No abstract is provided for this article.
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.
Land use system in Russia has been significantly changed since 1990. More than quarter of croplands (about 34 M ha) including soils of southern regions (Chernozems. Kastanozems) was abandoned. The abandonment of cultivated lands and successive establishment of natural vegetation led to carbon (C) accumulation in soil, qualitative changes in organic C pools and microbial community. This study was aimed (1) to quantify the different C organic pools (total, labile, recalcitrant, and microbial) in the former arable Chernozems depending on the abandonment period and (2) to estimate C sequestration potential of soils after land use change from crops to natural vegetation.
No abstract is provided for this article.
Summary Incorporation of labelled 15 N and 14 C amino acids and nucleic bases into soil humus fractions as well as humus turnover was investigated under field conditions. The dynamics of 15 N and 14 C incorporation into organic matter was characterized by the following main steps: rapid incorporation of the labelled substance prevailing for the first 1–3 weeks, and decomposition of included labelled fragments prevailing beyond one month after substance addition. The annual turnover rates of N and C in humus fractions due to incorporation of amino acids and nucleic bases were calculated. The turnover rate of N in humus is two to three times that of C. The contribution of amino acids to organic matter generation is about twice as great as that of nucleic bases and other N‐containing organic substances. This indicates the important role of amino acids in the humification process and humus turnover. Turnovers of humic acids (0·002 year −1 for C and 0·02 for N) are the most rapid of humic fractions investigated, and humin is characterized by the slowest turnover (0·0002 year −1 for C and 0·007 for N). There are no significant differences in the turnover rates of fulvic acid fractions (0·0002 year −1 for C) with different molecular weight.
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.
Increasing phosphorus (P) inputs induced by anthropogenic activities have increased P availability in soils considerably, with dramatic effects on carbon (C) cycling and storage. However, the underlying mechanisms via which P drives plant and microbial regulation of soil organic C (SOC) formation and stabilization remain unclear, hampering the accurate projection of soil C sequestration under future global change scenarios. Taking the advantage of an 8-year field experiment with increasing P addition levels in a subalpine forest on the eastern Tibetan Plateau, we explored plant C inputs, soil microbial communities, plant and microbial biomarkers, as well as SOC physical and chemical fractions. We found that continuous P addition reduced fine root biomass, but did not affect total SOC content. P addition decreased plant lignin contribution to SOC, primarily from declined vanillyl-type phenols, which was coincided with a reduction in methoxyl/N-alkyl C by 2.1%-5.5%. Despite a decline in lignin decomposition due to suppressed oxidase activity by P addition, the content of lignin-derived compounds decreased because of low C input from fine roots. In contrast, P addition increased microbial (mainly fungal) necromass and its contribution to SOC due to the slower necromass decomposition under reduced N-acquisition enzyme activity. The larger microbial necromass contribution to SOC corresponded with a 9.1%-12.4% increase in carbonyl C abundance. Moreover, P addition had no influence on the slow-cycing mineral-associated organic C pool, and SOC chemical stability indicated by aliphaticity and recalcitrance indices. Overall, P addition in the subalpine forest over 8 years influenced SOC composition through divergent alterations of plant- and microbial-derived C contributions, but did not shape SOC physical and chemical stability. Such findings may aid in accurately forecasting SOC dynamics and their potential feedbacks to climate change with future scenarios of increasing soil P availability in Earth system models.