Stem respiration and carbon dioxide efflux of young Populus deltoides trees in relation to temperature and xylem carbon dioxide concentration

Oecologia ◽  
2007 ◽  
Vol 154 (4) ◽  
pp. 637-649 ◽  
Author(s):  
An Saveyn ◽  
Kathy Steppe ◽  
Mary Anne McGuire ◽  
Raoul Lemeur ◽  
Robert O. Teskey
Plants ◽  
2020 ◽  
Vol 9 (2) ◽  
pp. 230 ◽  
Author(s):  
Thomas E. Marler ◽  
Murukesan V. Krishnapillai

Stem respiration is influenced by the vertical location of tree stems, but the influence of vertical location on stem respiration in a representative cycad species has not been determined. We quantified the influence of vertical strata on stem carbon dioxide efflux (Es) for six arborescent Cycas L. species to characterize this component of stem respiration and ecosystem carbon cycling. The influence of strata on Es was remarkably consistent among the species, with a stable baseline flux characterizing the full mid-strata of the pachycaulous stems and an increase in Es at the lowest and highest strata. The mid-strata flux ranged from 1.8 μmol·m−2·s−1 for Cycas micronesica K.D. Hill to 3.5 μmol·m−2·s−1 for Cycas revoluta Thunb. For all species, Es increased about 30% at the lowest stratum and about 80% at the highest stratum. A significant quadratic model adequately described the Es patterns for all six species. The increase of Es at the lowest stratum was consistent with the influence of root-respired carbon dioxide entering the stem via sap flow, then contributing to Es via radial conductance to the stem surface. The substantial increase in Es at the highest stratum is likely a result of the growth and maintenance respiration of the massive cycad primary thickening meristem that constructs the unique pachycaulous cycad stem.


2018 ◽  
Author(s):  
Oscar A. Douglas-Gallardo ◽  
Cristián Gabriel Sánchez ◽  
Esteban Vöhringer-Martinez

<div> <div> <div> <p>Nowadays, the search of efficient methods able to reduce the high atmospheric carbon dioxide concentration has turned into a very dynamic research area. Several environmental problems have been closely associated with the high atmospheric level of this greenhouse gas. Here, a novel system based on the use of surface-functionalized silicon quantum dots (sf -SiQDs) is theoretically proposed as a versatile device to bind carbon dioxide. Within this approach, carbon dioxide trapping is modulated by a photoinduced charge redistribution between the capping molecule and the silicon quantum dots (SiQDs). Chemical and electronic properties of the proposed SiQDs have been studied with Density Functional Theory (DFT) and Density Functional Tight-Binding (DFTB) approach along with a Time-Dependent model based on the DFTB (TD-DFTB) framework. To the best of our knowledge, this is the first report that proposes and explores the potential application of a versatile and friendly device based on the use of sf -SiQDs for photochemically activated carbon dioxide fixation. </p> </div> </div> </div>


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Karolina Kula ◽  
Agnieszka Kącka-Zych ◽  
Agnieszka Łapczuk-Krygier ◽  
Radomir Jasiński

Abstract The large and significant increase in carbon dioxide concentration in the Earth’s atmosphere is a serious problem for humanity. The amount of CO2 is increasing steadily which causes a harmful greenhouse effect that damages the Earth’s climate. Therefore, one of the current trends in modern chemistry and chemical technology are issues related to its utilization. This work includes the analysis of the possibility of chemical consumption of CO2 in Diels-Alder processes under non-catalytic and catalytic conditions after prior activation of the C=O bond. In addition to the obvious benefits associated with CO2 utilization, such processes open up the possibility of universal synthesis of a wide range of internal carboxylates. These studies have been performed in the framework of Molecular Electron Density Theory as a modern view of the chemical reactivity. It has been found, that explored DA reactions catalyzed by Lewis acids with the boron core, proceeds via unique stepwise mechanism with the zwitterionic intermediate. Bonding Evolution Theory (BET) analysis of the molecular mechanism associated with the DA reaction between cyclopentadiene and carbon dioxide indicates that it takes place thorough a two-stage one-step mechanism, which is initialized by formation of C–C single bond. In turn, the DA reaction between cyclopentadiene and carbon dioxide catalysed by BH3 extends in the environment of DCM, indicates that it takes place through a two-step mechanism. First path of catalysed DA reaction is characterized by 10 different phases, while the second by eight topologically different phases.


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