Effect of drought on soil microbial metabolisms driving carbon allocation and volatile organic compound cycling in the tropical rainforest at Biosphere 2

2022 ◽  
Author(s):  
Linnea Honeker ◽  
Giovanni Pugliese ◽  
Johannes Ingrisch ◽  
Jane Fudyma ◽  
Juliana Gil-Loaiza ◽  
...  
2020 ◽  
Author(s):  
Christiane Werner ◽  
Nemiah S. Ladd ◽  
Laura Meredith ◽  

<p>Ecosystem processes present a complex interplay between different components, such as vegetation, soil, and the rhizosphere. All these different components can emit (or even uptake) a plethora of volatile organic compound (BVOC) with highly dynamic response to environmental changes. However, processes controlling carbon allocation into primary and secondary metabolism such as VOC synthesis or respiratory CO<sub>2</sub> emission remain unclear. De novo synthesis of BVOC depends on the availability of carbon, as well as energy provided by primary metabolism. Thus, carbon allocation may compete between primary and secondary metabolism, which are linked via a number of interfaces including the central metabolite pyruvate. It is the main substrate fulling respiration, but also a substrate for a large array of secondary pathways leading to the biosynthesis of many volatile organic compounds, such as volatile isoprenoids, oxygenated VOCs. Within the European Research Council (ERC) Project VOCO we developed a novel technological basis to couple CO<sub>2</sub> fluxes with VOC emissions based on simultaneous real-time measurements of stable carbon isotope composition of branch, root, and soil respired CO<sub>2</sub> and VOC fluxes (Fasbender et al. 2018). Position specific <sup>13</sup>C-labeled pyruvate feeding experiments are used to trace partitioning within the metabolic branching points into VOCs versus CO<sub>2</sub> emissions, bridging scales from sub-molecular to whole-plant and ecosystem processes. Positional 13C-labelling will trace real-time sub-molecular carbon investment into VOCs and CO<sub>2</sub>, enabling mechanistic descriptions of the underlying biochemical pathways coupling anabolic and catabolic processes.</p><p>To trace ecosystem scale interactions, we implemented a whole-ecosystem labelling approach in the world’s largest controlled growth facility: the Biosphere 2 Tropical Rainforest. In the Biosphere 2 Water, Atmosphere, and Life Dynamics (B2-WALD) experiment, we applied an ecosystem scale drought and tracing carbon allocation and dynamics of VOC, CO<sub>2</sub> and H<sub>2</sub>O fluxes from leaf, root, soil and atmospheric scales. The overarching goal of B2-WALD is to track, biological mechanisms controlling the fate of CO<sub>2</sub>, VOC and water cycling in an ecosystem under change in an interdisciplinary approach. This comprehensive data set will be used for carbon and water partitioning from the metabolic to ecosystem scale</p><p>Fasbender L., et al. (<strong>2018</strong>). A novel approach combining PTR-TOF-MS, <sup>13</sup>CO<sub>2</sub> laser spectroscopy and <sup>13</sup>C-metabolite labelling to trace real-time carbon allocation into BVOCs and respiratory CO<sub>2</sub>. PLOS One,13: e0204398</p><p> </p>


2016 ◽  
Vol 15 (3) ◽  
pp. 251-259
Author(s):  
Shreedhar Devkota ◽  
◽  
Jin Oh Jo ◽  
Dong Lyong Jang ◽  
Young Jin Hyun ◽  
...  

Chemosensors ◽  
2021 ◽  
Vol 9 (5) ◽  
pp. 104
Author(s):  
Hung-Yang Kuo ◽  
Wei-Riu Cheng ◽  
Tzu-Heng Wu ◽  
Horn-Jiunn Sheen ◽  
Chih-Chia Wang ◽  
...  

This paper presents the synthesis and evaluation of a carbon molecular sieve membrane (CMSM) grown inside a MEMS-fabricated μ-preconcentrator for sampling highly volatile organic compounds. An array of µ-pillars measuring 100 µm in diameter and 250 µm in height were fabricated inside a microfluidic channel to increase the attaching surface for the CMSM. The surface area of the CMSM was measured as high as 899 m2/g. A GC peak amplification factor >2 × 104 was demonstrated with gaseous ethyl acetate. Up to 1.4 L of gaseous ethanol at the 100 ppb level could be concentrated without exceeding the capacity of this microchip device. Sharp desorption chromatographic peaks (<3.5 s) were obtained while using this device directly as a GC injector. Less volatile compounds such as gaseous toluene, m-xylene, and mesitylene appeared to be adsorbed strongly on CMSM, showing a memory effect. Sampling parameters such as sample volatilities, sampling capacities, and compound residual issues were empirically determined and discussed.


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