Increased litter input increases litter decomposition and soil respiration but has minor effects on soil organic carbon in subtropical forests

2015 ◽  
Vol 392 (1-2) ◽  
pp. 139-153 ◽  
Author(s):  
Xiong Fang ◽  
Liang Zhao ◽  
Guoyi Zhou ◽  
Wenjuan Huang ◽  
Juxiu Liu
2021 ◽  
Vol 18 (1) ◽  
pp. 1-11
Author(s):  
Lianlian Zhu ◽  
Zhengmiao Deng ◽  
Yonghong Xie ◽  
Xu Li ◽  
Feng Li ◽  
...  

Abstract. Litter decomposition plays a vital role in wetland carbon cycling. However, the contribution of aboveground litter decomposition to the wetland soil organic carbon (SOC) pool has not yet been quantified. Here, we conducted a Carex brevicuspis leaf litter input experiment to clarify the intrinsic factors controlling litter decomposition and quantify its contribution to the SOC pool at different water levels. The Carex genus is ubiquitous in global freshwater wetlands. We sampled this plant leaf litter at −25, 0, and +25 cm relative to the soil surface over 280 d and analysed leaf litter decomposition and its contribution to the SOC pool. The percentage litter dry weight loss and the instantaneous litter dry weight decomposition rate were the highest at +25 cm water level (61.8 %, 0.01307 d−1), followed by the 0 cm water level (49.8 %, 0.00908 d−1), and the lowest at −25 cm water level (32.4 %, 0.00527 d−1). Significant amounts of litter carbon, nitrogen, and phosphorus were released at all three water levels. Litter input significantly increased the soil microbial biomass and fungal density but had nonsignificant impacts on soil bacteria, actinomycetes, and the fungal∕bacterial concentrations at all three water levels. Compared with litter removal, litter addition increased the SOC by 16.93 %, 9.44 %, and 2.51 % at the +25, 0, and −25 cm water levels, respectively. Hence, higher water levels facilitate the release of organic carbon from leaf litter into the soil via water leaching. In this way, they increase the soil carbon pool. At lower water levels, soil carbon is lost due to the slower litter decomposition rate and active microbial (actinomycete) respiration. Our results revealed that the water level in natural wetlands influenced litter decomposition mainly by leaching and microbial activity, by extension, and affected the wetland surface carbon pool.


2020 ◽  
Author(s):  
Lianlian Zhu ◽  
Zhengmiao Deng ◽  
Yonghong Xie ◽  
Xu Li ◽  
Feng Li ◽  
...  

Abstract. Litter decomposition plays a vital role in wetland carbon cycling. However, the contribution of aboveground litter decomposition to the wetland soil organic carbon (SOC) pool has not yet been quantified. Here, we conducted a Carex brevicuspis leaf litter input experiment to clarify the intrinsic factors controlling litter decomposition and quantify it's contribution to SOC pool at different water levels. This species is ubiquitous to global freshwater wetlands. We sampled this plant leaf litter at −25, 0, and +25 cm relative to the soil surface over 280 days and analysed leaf litter decomposition and its contribution to the SOC pool. The mass loss and carbon release rates were the highest at +25 cm water level, followed by the 0 cm water level. The rates of these parameters were the lowest at −25 cm water level. Significant amounts of litter carbon, nitrogen, and phosphorus were released at all three water levels. Litter input significantly increased the soil microbial biomass and fungal density but had nonsignificant impacts on soil bacteria, actinomycetes, and fungal/bacterial concentrations at all three water levels. Compared with litter removal, litter application increased the SOC by 25.12 %, 9.58 %, and 4.98 % at the +25 cm, 0 cm, and −25 cm water levels, respectively. Hence, higher water levels facilitate the release of organic carbon from leaf litter into the soil via water leaching. In this way, they strengthen the soil carbon pool. At lower water levels, soil carbon is lost as the slower litter decomposition rate and active microbial (actinomycete) respiration. Our results revealed that the water level in natural wetlands influences litter decomposition mainly by leaching and microbial activity, by extension, affects wetland surface carbon pool.


2019 ◽  
Vol 8 (1) ◽  
Author(s):  
Tong Li ◽  
Haicheng Zhang ◽  
Xiaoyuan Wang ◽  
Shulan Cheng ◽  
Huajun Fang ◽  
...  

2020 ◽  
Vol 707 ◽  
pp. 136104 ◽  
Author(s):  
Mengxiao Yu ◽  
Ying-Ping Wang ◽  
Jeffrey A. Baldock ◽  
Jun Jiang ◽  
Jiangming Mo ◽  
...  

2012 ◽  
Vol 28 (2) ◽  
pp. 239-248 ◽  
Author(s):  
Nirav Mehta ◽  
J. Dinakaran ◽  
Shrena Patel ◽  
A. H. Laskar ◽  
M. G. Yadava ◽  
...  

2021 ◽  
Author(s):  
Gerardo Ojeda ◽  
Hernando García ◽  
Susanne Woche ◽  
Jorg Bachmann ◽  
Georg Guggenberger ◽  
...  

<p><strong>Contextualization</strong>: In 2011, it was published a curious conundrum, which forms the basis of the present study: why, when organic matter is thermodynamically unstable, does it persist in soils, sometimes for thousands of years? The question challenges the idea that the recalcitrant or labile character of soil organic matter (SOM) is a sufficient argument to ensure SOM persistence. Temperature could play an important role in SOM decomposition, especially in tropics. Particularly, tropical dry forest (TDF) represents an important ecosystem with unique biodiversity and fertile soils in Colombia. At present, the increase in population density and consequently, in the demands of energy and arable land, have led to its degradation.</p><p> </p><p><strong>Knowledge gap</strong>: Although the mentioned question was formulated several years ago, it has still to be answered, hence limiting the development of new soil organic carbon (SOC) models or the quantification of its ecosystem services. A key point, in terms of soil carbon storage, is to determine the maximum rate of CO<sub>2</sub> emissions from soils (Rmax). Traditionally, it is considered that Rmax occurs at the 50% of field capacity. Unfortunately, information about the environmental conditions under which this maximum occurs is scarce.</p><p><strong> </strong></p><p><strong>Purpose</strong>: The main objectives of this study were: (a) determine the maximum rate of soil respiration or CO<sub>2</sub> emissions from soil in TDF soils and (b) to estimate the main environmental drivers of maximum SOM decomposition along a temperature gradient (20°, 30°, 40°C) in incubated soils.</p><p><strong> </strong></p><p><strong>Methodology</strong>: Soils pertained to permanent plots were sampled in six different TDF of Colombia. The evolution of CO<sub>2</sub> emissions (monitored by an infrared gas analyser), relative humidity and soil temperature were recorded in time on incubated soils samples. Temperature was maintained constant at 20°C, 30°C and 40°C during soil incubations under soil drying conditions. Additionally, elemental composition (Fe, Ca, O, Al, Si, K, Mg, Na) of SOM and chemical composition of soil organic carbon (SOC: aromatic-C, O-alkyl-C, Aliphatic-C, Phenolic and Ketonic-C) were determined by X-ray photoelectron spectroscopy (XPS).</p><p><strong> </strong></p><p><strong>Results and conclusions</strong>: The majority of TDF soil samples (90.7%) presented that its peak of CO<sub>2</sub> emissions occurs at soil-water contents higher than saturation (0 MPa), at 20°, 30° and 40°C. Clearly, to consider that the maximum soil respiration rate could be observed at the 50% of field capacity, underestimated the real maximum value of carbon mineralization (48-68%.) Globally, increases in the Rmax values corresponded to increases in electrical conductivity, soil desorption rates, total carbon and nitrogen contents, and decreases in bulk density (BD) and aggregate stability. Taking into account the temperature gradient, increments in calcium and aromatic carbon contents corresponded to decrements in Rmax values but only at 30°C and 40°C, respectively. Some authors indicated that at high soil moisture contents, iron reduction could be release protected carbon. However, no significant relation between Fe and Rmax was observed. Consequently, physical and chemical properties related to SOM accessibility and decomposability by microbial activity, were the main drivers and controls of maximum SOM decomposition rates.</p>


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