Carbon partitioning in a wet and a semiwet subarctic mire ecosystem based on in situ 14C pulse-labelling

2011 ◽  
Vol 43 (2) ◽  
pp. 231-239 ◽  
Author(s):  
Maria Olsrud ◽  
Torben R. Christensen
2016 ◽  
Vol 49 (2) ◽  
pp. 399-414 ◽  
Author(s):  
I. B. Timokhina ◽  
K. D. Liss ◽  
D. Raabe ◽  
K. Rakha ◽  
H. Beladi ◽  
...  

In situ neutron diffraction, transmission electron microscopy (TEM) and atom probe tomography (APT) have been used to study the early stages of bainite transformation in a 2 mass% Si nano-bainitic steel. It was observed that carbon redistribution between the bainitic ferrite and retained austenite at the early stages of the bainite transformation at low isothermal holding occurred in the following sequence: (i) formation of bainitic ferrite nuclei within carbon-depleted regions immediately after the beginning of isothermal treatment; (ii) carbon partitioning immediately after the formation of bainitic ferrite nuclei but substantial carbon diffusion only after 33 min of bainite isothermal holding; (iii) formation of the carbon-enriched remaining austenite in the vicinity of bainitic laths at the beginning of the transformation; (iv) segregation of carbon to the dislocations near the austenite/ferrite interface; and (v) homogeneous redistribution of carbon within the remaining austenite with the progress of the transformation and with the formation of bainitic ferrite colonies. Bainitic ferrite nucleated at internal defects or bainite/austenite interfaces as well as at the prior austenite grain boundary. Bainitic ferrite has been observed in the form of an individual layer, a colony of layers and a layer with sideplates at the early stages of transformation.


1992 ◽  
Vol 28 (1) ◽  
pp. 73-80 ◽  
Author(s):  
L. Walter ◽  
R. Altenburger ◽  
R. Callies ◽  
L. H. Grimme ◽  
D. Leibfritz ◽  
...  

2020 ◽  
Author(s):  
Dorine Desalme ◽  
Ornuma Duangngam ◽  
Philippe Thaler ◽  
Poonpipope Kasemsap ◽  
Jate Sathornkich ◽  
...  

<p>Rubber trees (<em>Hevea brasiliensis</em>) are the main source of natural rubber, extracted from latex, which exudes from the trunk after tapping. Tapped trees require large amounts of carbon (C) to regenerate the latex after its collection. Knowing the contribution of C sources involved in latex biosynthesis will help understand how rubber trees face this additional C demand. Whole crown<sup> 13</sup>CO<sub>2 </sub>pulse labelling was performed on 4-year-old rubber trees in June when latex production was low and in October, when it was high. <sup>13</sup>C contents were quantified in the foliage, phloem sap, wood and latex. In both labelling periods, <sup>13</sup>C was recovered in latex just after labelling, indicating that part of the carbohydrates was directly allocated to latex. However, significant <sup>13</sup>C amounts were still recovered in latex after 100 days and the peak was reached significantly later than in phloem sap, demonstrating the contribution of a reserve pool as a source of latex C. The contribution of new photosynthates to latex regeneration was faster and higher when latex metabolism was well established, in October than in June. An improved understanding of C dynamics and source-sink relationship in rubber tree is crucial to adapt tapping system practices and ensure sustainable latex production.</p>


Polar Biology ◽  
2012 ◽  
Vol 35 (8) ◽  
pp. 1209-1219 ◽  
Author(s):  
Jens-Arne Subke ◽  
Andreas Heinemeyer ◽  
Harry W. Vallack ◽  
Vincenzo Leronni ◽  
Robert Baxter ◽  
...  
Keyword(s):  

Soil Research ◽  
2005 ◽  
Vol 43 (5) ◽  
pp. 659 ◽  
Author(s):  
Bhupinderpal-Singh ◽  
M. J. Hedley ◽  
S. Saggar

Information on the dynamics of recently photo-assimilated carbon (C) allocated to roots and root-derived exudates in soils is scarce and experimentally difficult to obtain. We used Rhizon Soil Moisture SamplersTM (RSMS) placed at different depths in soil (20, 40, 80, 120 mm) to monitor short-term dynamics of root and root-derived C at the root–soil interface after 14CO2 pulse-labelling of pasture cores. At the 20 mm depth, 14C activity in soil solution peaked within 2 h of 14CO2 application. The peak of 14C activity took longer to appear and slower to disappear with increased depth. Negligible amounts of 14C as soluble exudates were found in the soil solution. The pattern of initial 14C activity in soil solution, allocation of recently assimilated 14C in roots, and root mass distribution with depth were closely related to each other. This suggested that the rapid appearance of 14CO2 in soil solution is more closely linked to root respiration of recent 14C-assimilates (transferred via shoots to roots) and/or to microbial decomposition of root-released 14C-assimilates than to transfer by diffusion of atmospheric 14CO2 through open soil surface to different depths in soil. The use of RSMS was an effective, simple, and non-destructive method to monitor the dynamics of root-derived 14C by in situ sampling of soil solution.


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