Who is who in litter decomposition




















Moreover, we employed metaproteomics to investigate the influence of environmental factors and nutrients on the decomposer structure and function during beech litter decomposition. Litter was collected at forest sites in Austria with different litter nutrient content.

Mass spectra were assigned to phylogenetic and functional groups by a newly developed bioinformatics workflow, assignments being validated by complementary approaches.

Three of the sampled fields are referred to as recently abandoned fields, since they have been abandoned from agricultural practices for 5—9 years. The other field sites have been abandoned for 29—32 years and are therefore referred to as long-term abandoned fields. Details of these study sites are given in Table 1. Soil sampling took place in October by collecting eight soil samples 10 cm deep, 6 cm diameter per ex-arable field.

Soil samples were taken at least 20 m from the edge of a field, and at least 10 m apart. Aboveground vegetation was removed prior to transportation. TABLE 1. Overview of ex-arable field sites where soil samples were taken, including information on the exact location, land abandonment stage and time of abandonment of agricultural practices.

In the summer of , ten soil cores 12 cm diameter, 20 cm deep were collected per field site, including standing vegetation.

Nine of those cores were transported to the laboratory and labeled with The remaining core served as a non-labeled control core. The labeled plant material was used as a 13 C-labeled substrate in the incubation experiment see below and is further referred to as 13 C-labeled litter.

Soil samples were sieved 2 mm to remove roots and stones and subsequently pooled into one composite soil sample per field site. For each of the six field sites, a total of 30 glass bottles of ml were filled with an equivalent of 50 g of dry weight soil.

Three out of every five bottles were supplemented with 0. The bottles were closed with a cotton ball to avoid contamination, while permitting gas exchange and incubated in the dark at One-sixth of all bottles was destructively sampled at each of the following time points: 1, 3, 7, 14, 28, and 56 days. Per field site, this corresponded to three labeled samples technical replicates , plus a positive and negative control sample.

During the entire experimental period of 56 days, 13 CO 2 flux measurements were taken. The 30 bottles that were harvested on day 56 were subjected to gas sampling throughout the entire experiment. On day 1, 3, 7, 14, 28, and 55 because of destructive sampling on day 56 , the cotton balls were removed from the bottles and subsequently closed with a lid with a rubber septum. The headspace air pressure-drop was compensated by injecting 15 ml of N 2 gas.

A total number of 24 PLFA biomarkers were used to study soil microbial community composition and to calculate total microbial biomass. Within 24 h of sampling, soil samples were extracted with ml 0. Samples were shaken for 1 h at rpm on a rotary shaker Laboshake, Gerhardt, Germany.

Samples were centrifuged for 4 min at rpm Megafuge 1. Results were analyzed using R version 3. To visualize the sequential order of microbial groups throughout the first stages of litter decomposition, the excess amount of 13 C in different microbial groups was normalized over time using the following formula:. Absolute value transformation was applied to meet homogeneity and normality requirements. Comparison of all control samples no litter addition based on abundance of phospholipid fatty acid PLFA biomarkers revealed an effect of land abandonment stage on the composition of the soil microbial community Figure 1.

When looking at the relative abundances for individual biomarkers, more than half of all biomarkers showed a marginally significant higher abundance in long-term abandoned soils compared to recently abandoned soils Supplementary Table S1. Principal component analysis PCA of the relative abundance of soil microbial PLFA biomarkers to characterize soil microbial community composition.

TABLE 2. Soil microbial community abundances and ratios based on PLFA biomarkers for each land abandonment stage recent and long-term. One day after the addition of 13 C-labeled litter there was more than a tenfold increase in the total amount of respired CO 2 , which gradually decreased back to the control level over the course of the experiment Table 3.

The absolute and relative amounts of litter-derived CO 2 were not significantly different between the different land abandonment stages, although there were significant interaction effects between land abandonment stage and time. The total amount of mineral N in recently abandoned soils decreased compared to the control treatment until day 7, while the mineral N content for long-term abandoned soils showed an initial increase followed by a similar trend as observed for recently abandoned soils Table 3.

After day 7, the amount of mineral N increased until the end of the incubation experiment Table 3. No significant differences were found in mineral N dynamics between recent and long-term abandoned soils.

TABLE 3. Carbon and nitrogen mineralization parameters for recent and long-term abandoned ex-arable soils during incubation at each respective sampling moment. One day after the addition of 13 C-labeled litter, the total amount of PLFA in both recent and long-term abandoned soils increased from approximately to more than nmol C per gram soil. After day 3, the total amount of PLFA biomass gradually decreased, so that at day 56 the amount of PLFA biomass was still slightly increased compared to the situation without litter addition.

Similar patterns were observed when examining individual PLFA biomarkers, where only a few biomarkers were significantly affected by land abandonment stage during the incubation experiment when testing for PLFA biomass Supplementary Table S2 and the absolute amount of litter-derived PLFA biomass Supplementary Table S3. Dotted lines show the corresponding control PLFA biomass without litter addition.

These analyses reveal a strong time effect during the incubation experiment for all three microbial community properties, whereby only the relative amount of litter-derived PLFA was clearly affected by land-abandonment stage Figure 3C. Principal component analyses of phospholipid fatty acids PLFA biomarkers to characterize soil microbial community structure in ex-arable soils recent abandonment, orange vs.

There were no significant effects of land abandonment stage on the absolute amount of litter-derived PLFA biomass for any of the microbial groups.

TABLE 4. When examining the build-up of litter-derived PLFA biomass in Figure 2 , we found that each microbial group had its own distinct substrate derived 13 C incorporation pattern over time.

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Also it is very difficult to understand the rate of litter degradation as it is influenced by a number of entirely different factors. Researchers are yet to finalise a methodology to detect the rate of litter degradation, which can incorporate all the factors. However, it is significant to study litter degradation in the context of increasing anthropogenic impacts on biogeochemical cycles. This review focuses on various factors that affect the litter degradation and degradation patterns of the various polymers in leaf litter.

It also emphasised and discussed various methods for assessing litter degradation. The review found that there are very few studies on litter degradation and element recycling in various ecosystems. Hence, future research must be centralised on the following subject areas: a development of a methodology for assessing the rate of litter degradation; b litter degradation and climate change; c transport pathways of elements during litter degradation, etc.

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