No abstract is provided for this article.
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No abstract is provided for this article.
No abstract is provided for this article.
No abstract is provided for this article.
Obwohl Sorption an Mineraloberflachen als dominierender Prozess zur Erklarung des langsamen Umsatzes mineralassoziierter organischer Bodensubstanz (OBS) dient, widerspricht diese Idee einer zunehmenden Zahl an Inkubationsstudien, die zeigen, dass fur niedermolekulare Substanzen nicht nur die mikrobielle Aufnahme kompetitivier als die Sorption ist, sondern auch sorbierte Substanzen in hohem Mase desorbiert und mikrobiell verwertet werden konnen. Dabei wurde gezeigt, dass sich die Verstoffwechselung desorbierter Substanzen zugunsten eines erhohten Recyclings verschiebt. Dies wirft die Frage auf, ob Recycling von intakten Metaboliten, d.h. unter Erhalt des Kohlenstoffgerustes, generell ein bisher stark unterschatzter Prozess ist, der die relativ hohen 14C Alter der OBS teilweise erklaren kann. Nach Applikation hoher Toxindosen konnte nachgewiesen werden, dass die nachfolgende Reetablierung der mikrobiellen Gemeinschaft zu grosem Anteil auf Recycling der Nekromasskomponenten der Vorgeneration basiert. Intaktes Metabolitrecycling ist jedoch unter steady-state Bedingungen nur auserst schwierig von der direkten Stabiliserung zu unterscheiden. Um diesen Prozess im Fliesgleichgewicht nachzuweisen muss 1) ein Biomolekul untersucht werden, dessen Biosyntheseweg so aufwandig ist, dass Recycling einen deutlichen Vorteil fur die Zelle im Vergleich zur Neusynthese darstellt, 2) dieses Biomolkul in lebenden Zellen in einer anderen Form gebunden sein, als die zu recycelnde Einheit in der Bodenlosung, so dass beide Zustandsformen unterschieden werden konnen und 3) dieses Biomolekul positionsspezifisch isotopenmarkiert zugegeben werden, so dass uber einen identischen Einbau der Positionen die Intaktheit des Kohlenstoffgerustes nachgewiesen werden kann. Am Beispiel der Alkylketten von Fettsauren, die in mikrobiellen Zellen primar als Phospholipide in den Membranen gebunden sind, soll dieses Prinzip veranschaulicht werden. Eine erste Abschatzung des intakten Recyclings von Alkylketten durch Mikroorganismen in Boden zeigt, dass von den 0.03% der basierend auf Alkyl-Kohlenstoff neugebildeten PLFA mehr als 75% aus intaktem Recycling dieser Ketten hervor gingen. Obwohl der Beitrag des Recyclings intakter Metabolite zur Umsatzzeit der gesamten OBS aufgrund der geringen Anzahl bisher untersuchter Metabolite noch nicht final quantifiziert werden kann, untermauern die hier vorgestellten Ergebnisse jedoch die hohe Relevanz dieses Prozesses fur die Dynamik der OBS.
The effects of tree species on the N cycle in forest systems are still under debate. However, contradicting results of different 15 N labeling techniques of trees and N tracers in the individual studies hamper a generalized mechanistic view. Therefore, we compared Ca( 15 NO 3 ) 2 and 15 NH 4 Cl leaf‐labeling method to investigate: (1) N allocation patterns from aboveground to belowground, (2) the cycles of N in soil‐plant systems, and (3) to allow the production of highly 15 N enriched litter for subsequent decomposition studies. 20 beeches ( Fagus sylvatica ) and 20 ashes ( Fraxinus excelsior ) were 15 N pulse labeled from aboveground with Ca( 15 NO 3 ) 2 and 40 beeches and 40 ashes were 15 N pulse labeled from aboveground with 15 NH 4 Cl. 15 N was quantified in tree compartments (leaves, stem, roots) and in soil after 8 d. Beech and ash incorporated generally more 15 N from the applied 15 NH 4 Cl compared to Ca( 15 NO 3 ) 2 in all measured compartments, except for ash leaves. Ash had highest 15 N incorporation [45% of the applied with Ca( 15 NO 3 ) 2 ] in its leaves. Both tree species kept over 90% of all fixed 15 N from Ca( 15 NO 3 ) in their leaves, whereas only 50% of the 15 N from the 15 NH 4 Cl tracer remained in the leaves and 50% were allocated to stem, roots, and soil. There was no damage of the leaves by both salts, and thus both 15 N tracers enable long‐term labeling in situ field studies on N rhizodeposition and allocation in soils. Nonetheless, the 15 N incorporation by both salts was species specific: the leaf labeling with 15 NH 4 Cl results in a more homogenous distribution between the tree compartments in both tree species and, therefore, 15 NH 4 Cl is more appropriate for allocation studies. The leaf labeling with Ca( 15 NO 3 ) 2 is a suitable tool to produce highly enriched 15 N leaf litter for further long term in situ decomposition and turnover studies.
Plants allocate carbon (C) to sink tissues depending on phenological, physiological or environmental factors. We still have little knowledge on C partitioning into various cellular compounds and metabolic pathways at various ecophysiological stages. We used compound-specific stable isotope analysis to investigate C partitioning of freshly assimilated C into tree compartments (needles, branches and stem) as well as into needle water-soluble organic C (WSOC), non-hydrolysable structural organic C (stOC) and individual chemical compound classes (amino acids, hemicellulose sugars, fatty acids and alkanes) of Norway spruce (Picea abies) following in situ 13C pulse labelling 15 days after bud break. The 13C allocation within the above-ground tree biomass demonstrated needles as a major C sink, accounting for 86% of the freshly assimilated C 6 h after labelling. In needles, the highest allocation occurred not only into the WSOC pool (44.1% of recovered needle 13C) but also into stOC (33.9%). Needle growth, however, also caused high 13C allocation into pathways not involved in the formation of structural compounds: (i) pathways in secondary metabolism, (ii) C-1 metabolism and (iii) amino acid synthesis from photorespiration. These pathways could be identified by a high 13C enrichment of their key amino acids. In addition, 13C was strongly allocated into the n-alkyl lipid fraction (0.3% of recovered 13C), whereby 13C allocation into cellular and cuticular exceeded that of epicuticular fatty acids. 13C allocation decreased along the lipid transformation and translocation pathways: the allocation was highest for precursor fatty acids, lower for elongated fatty acids and lowest for the decarbonylated n-alkanes. The combination of 13C pulse labelling with compound-specific 13C analysis of key metabolites enabled tracing relevant C allocation pathways under field conditions. Besides the primary metabolism synthesizing structural cell compounds, a complex network of pathways consumed the assimilated 13C and kept most of the assimilated C in the growing needles.