Very precise measurement of carbon dioxide atmospheric concentration by using TDLs

Author(s):  
Francesco D'Amato ◽  
Antonio Lancia ◽  
Peter W. Werle
2017 ◽  
pp. 185-188
Author(s):  
András Tamás ◽  
Ágnes Törő ◽  
Tamás Rátonyi ◽  
Endre Harsányi

The atmospheric concentration of carbon dioxide increases from decade to decade in increasing pace. In 1957, atmospheric carbon dioxide levels were around 315 ppm, while in 2012 it amounted to 394.49 ppm concentration. In parallel, the global temperature is rising,which is projected to average 1.5–4.5 °C. The carbon dioxide concentration is a key factor – in interaction with the light – affects the plant's photosynthesis. Among the various factors significant interactions prevail: environmental factors affect - the growth and the development of plants, leaf area size and composition, the function of the photosynthetic apparatus, the duration of growing season.


Author(s):  
Philip M. Fearnside

Climate changes predicted for Brazilian Amazonia place much of the forest in danger of dieoff from the combined effect of drought and heat within the current century, and much sooner for some areas. Increases are expected in the frequency and magnitude of droughts from both the El Niño phenomenon and from the Atlantic dipole. These changes imply increased frequency of forest fires. Forest death from drought, fires or both would be followed by a transformation either to a savanna or to some type of low-biomass woody vegetation, in either case with greatly reduced biodiversity. This risk provides justification for Brazil to change its negotiating positions under the Climate Convention to accept a binding target now for national emissions and to support a low atmospheric concentration of carbon dioxide (400 ppmv or less) as the definition of “dangerous” interference with the climate system.


2019 ◽  
Vol 44 (4) ◽  
pp. 291-299 ◽  
Author(s):  
V. M. Ivakhov ◽  
N. N. Paramonova ◽  
V. I. Privalov ◽  
A. V. Zinchenko ◽  
M. A. Loskutova ◽  
...  

2018 ◽  
Vol 176 ◽  
pp. 05045 ◽  
Author(s):  
Erwan Cadiou ◽  
Jean-Baptiste Dherbecourt ◽  
Guillaume Gorju ◽  
Jean-Michel Melkonian ◽  
Antoine Godard ◽  
...  

We report on ground-based atmospheric concentration measurements of carbon dioxide, using a pulsed direct detection differential absorption lidar operating at 2051 nm. The transmitter is based on a tunable parametric source emitting 10-mJ energy, 10-ns duration Fourier-limited pulses. Range resolved concentration measurements have been carried out on the aerosol back-scattered signal. Cloud signals have been used to get long range integrated-path measurements.


2020 ◽  
Author(s):  
Chris R Taylor ◽  
Ben Keane ◽  
Iain Hartley ◽  
Gareth Phoenix

<p>Terrestrial ecosystems absorb 30% of anthropogenic carbon dioxide (CO<sub>2</sub>) emissions, slowing its rising atmospheric concentration and substantially inhibiting climate change. This uptake is believed to be due to elevated CO<sub>2</sub> (eCO<sub>2</sub>) stimulating plant photosynthesis and growth, thus increasing carbon (C) storage in plants and soil organic matter. However, nitrogen (N) limitation can reduce ecosystem C uptake capacity under eCO<sub>2</sub> by as much as 50%. Phosphorus (P) limitation in ecosystems is almost as common as N-limitation and is increasing due to ongoing deposition of N from anthropogenic activities. Despite this, we do not know how P-limited ecosystems will respond to eCO<sub>2</sub>, constituting a major gap in our understanding of how large areas of the biosphere will impact atmospheric CO<sub>2</sub> over the coming decades.</p><p>In the first study conducted into the effect of eCO<sub>2</sub> on P-limited ecosystems with manipulated nutrient availability, the Phosphorus Limitation And ecosystem responses to Carbon dioxide Enrichment project (PLACE), investigates the effects of eCO<sub>2</sub> on C cycling in grasslands, which are a critical global C store. Turf mesocosms from P-limited acidic and limestone grasslands, where N and P inputs have been manipulated for 20 years (control, low N (3.5 g m<sup>-2</sup> y<sup>-1</sup>), high N (14 g m<sup>-2</sup> y<sup>-1</sup>), and P (3.5 g m<sup>-2</sup> y<sup>-1</sup>)), have been exposed to either ambient or eCO<sub>2</sub> (600 ppm) in a miniFACE (mini Free Air Carbon Enrichment) system. Long-term P addition has alleviated P limitation while N additions have exacerbated it. The two contrasting grasslands contain different amounts of organic versus mineral P in their soils and, thus, plants may have to use contrasting strategies to acquire the additional P they need to increase growth rates under elevated CO<sub>2</sub>.</p><p>We present data from the first two growing seasons, including above and below ground productivity, and C, N and P cycling through plant, soil and microbial pools. Aboveground harvest data from the second year have shown eCO<sub>2</sub> has only increased biomass production in the limestone grassland (by 17%; p< 0.0001), and not in the acid grassland. There was also a significant effect of nutrient treatment (p< 0.001) with biomass increasing under P and HN, indicating some co-NP limitation. Stable isotope tracing, using the fumigation CO<sub>2</sub> signal has shown the fate of newly assimilated C and its contribution to gaseous C flux to the atmosphere in the form of methane (CH<sub>4</sub>) and respired CO<sub>2</sub>.  In summary, our first two years of eCO<sub>2</sub> treatment suggests that productivity of limestone and acidic grassland respond differently and that these responses depend on nutrient availability, indicating the complexity of predicting P-limited ecosystem responses as atmospheric CO<sub>2 </sub>continues to rise.</p>


1997 ◽  
Vol 26 (3) ◽  
pp. 239-240
Author(s):  
Shigeto Sudo ◽  
Takeshi Tominaga ◽  
Yoshihiro Makide

2008 ◽  
Vol 12 (9) ◽  
pp. 1-23 ◽  
Author(s):  
R. K. Kaufmann ◽  
L. F. Paletta ◽  
H. Q. Tian ◽  
R. B. Myneni ◽  
R. D. D’Arrigo

Abstract Two hypotheses are tested: 1) monitoring stations (e.g., Mauna Loa) are not able to measure changes in atmospheric concentrations of CO2 that are generated by changes in terrestrial vegetation at distant locations; 2) changes in the atmospheric concentration of carbon dioxide do not affect terrestrial vegetation at large scales under conditions that now exist in situ, by estimating statistical models of the relationship between satellite measurements of the normalized difference vegetation index (NDVI) and the atmospheric concentration of carbon dioxide measured at Mauna Loa and Point Barrow. To go beyond simple correlations, the notion of Granger causality is used. Results indicate that the authors are able to identify locations where and months when disturbances to the terrestrial biota “Granger cause” atmospheric CO2. The authors are also able to identify locations where and months when disturbances to the atmospheric concentration of carbon dioxide generate changes in NDVI. Together, these results provide large-scale support for a CO2 fertilization effect and an independent empirical basis on which observations at monitoring stations can be used to test hypotheses and validate models regarding effect of the terrestrial biota on atmospheric concentrations of carbon dioxide.


2019 ◽  
Author(s):  
Omid Taheri Qazvini ◽  
Shane G. Telfer

<p>Efficient and sustainable methods for carbon dioxide (CO<sub>2</sub>) capture are essential. Its atmospheric concentration must be reduced to meet climate change targets, and its removal from sources such as chemical feedstocks is vital. While mature technologies involving chemical reactions that absorb CO<sub>2</sub> exist, they have many drawbacks. Porous materials with void spaces that are complementary in size and electrostatic potential to CO<sub>2</sub> offer an alternative. In these materials, the molecular CO<sub>2 </sub>guests are trapped by noncovalent interactions, hence they can be recycled by releasing the CO<sub>2</sub> with a low energy penalty. Capacity and selectivity are the twin challenges for such porous adsorbents. Here, we show how a metal-organic framework, termed MUF-16 (MUF = Massey University Framework), is a universal adsorbent for CO<sub>2</sub> that sequesters large quantities of CO<sub>2</sub> from a broad palette of gas streams with record selectivities over competing gases. The crystallographically-determined position of the CO<sub>2</sub> molecules captured in the framework pores illustrate how complementary noncovalent interactions envelop CO<sub>2</sub> while repelling other guest molecules. The low affinity of the pore environment for other gases underpins the strikingly high selectivity of MUF-16 for CO<sub>2</sub> over methane, nitrogen, hydrogen, acetylene, ethylene, ethane, propylene and propane. Breakthrough gas separations under dynamic conditions benefit from short time lags in the elution of the weakly-adsorbed component to deliver a repertoire of high-purity products. MUF-16 is an inexpensive, robust, recyclable adsorbent that is universally applicable to the removal of CO<sub>2 </sub>from sources such as natural gas, syngas, flue gas and chemical feedstocks.</p><br>


2019 ◽  
Author(s):  
Omid Taheri Qazvini ◽  
Shane G. Telfer

<p>Efficient and sustainable methods for carbon dioxide (CO<sub>2</sub>) capture are essential. Its atmospheric concentration must be reduced to meet climate change targets, and its removal from sources such as chemical feedstocks is vital. While mature technologies involving chemical reactions that absorb CO<sub>2</sub> exist, they have many drawbacks. Porous materials with void spaces that are complementary in size and electrostatic potential to CO<sub>2</sub> offer an alternative. In these materials, the molecular CO<sub>2 </sub>guests are trapped by noncovalent interactions, hence they can be recycled by releasing the CO<sub>2</sub> with a low energy penalty. Capacity and selectivity are the twin challenges for such porous adsorbents. Here, we show how a metal-organic framework, termed MUF-16 (MUF = Massey University Framework), is a universal adsorbent for CO<sub>2</sub> that sequesters large quantities of CO<sub>2</sub> from a broad palette of gas streams with record selectivities over competing gases. The crystallographically-determined position of the CO<sub>2</sub> molecules captured in the framework pores illustrate how complementary noncovalent interactions envelop CO<sub>2</sub> while repelling other guest molecules. The low affinity of the pore environment for other gases underpins the strikingly high selectivity of MUF-16 for CO<sub>2</sub> over methane, nitrogen, hydrogen, acetylene, ethylene, ethane, propylene and propane. Breakthrough gas separations under dynamic conditions benefit from short time lags in the elution of the weakly-adsorbed component to deliver a repertoire of high-purity products. MUF-16 is an inexpensive, robust, recyclable adsorbent that is universally applicable to the removal of CO<sub>2 </sub>from sources such as natural gas, syngas, flue gas and chemical feedstocks.</p><br>


2016 ◽  
Vol 58 ◽  
pp. 35-41
Author(s):  
Irfan Mahmood ◽  
Muhammad Farooq Iqbal ◽  
Muhammad Imran Shahzad ◽  
Ahmed Waqas ◽  
Luqman Atique

Carbon dioxide (CO2), Methane (CH4) are two most potent greenhouse gases and are major source of climate change. Human activities particularly fossil fuels burning have caused considerable increase in atmospheric concentrations of greenhouse gases. CO2contributes 60% of anthropogenic greenhouse effect whereas CH4contributes 15%. Ice core records also show that the concentrations of Carbon dioxide and methane have increased substantially. The emission of these gases alters the Earth’s energy budget and are drivers of climate change. In the present study, atmospheric concentration of CO2and CH4over Pakistan is measured using Atmospheric Infrared Sounder (AIRS). Time series and time averaged maps are prepared to measure the concentrations of CO2and CH4. The results show considerable increase in concentration of Carbon dioxide and methane. The substantial increase in these concentrations can affect human health, earth radiative balance and can damage crops.


Sign in / Sign up

Export Citation Format

Share Document