Elsevier

Soil Biology and Biochemistry

Volume 43, Issue 9, September 2011, Pages 1808-1811
Soil Biology and Biochemistry

Resilience of microbial respiration, respiratory quotient and stable isotope characteristics to soil hydrocarbon addition

https://doi.org/10.1016/j.soilbio.2010.09.026Get rights and content

Abstract

On the basis of CO2 evolution rate, O2 uptake rate, and 13C isotopic signature of respired CO2, the metabolic response to the addition of 13C labelled n-hexadecane and palmitic acid each with supplementary nitrogen was studied for two topsoils, one under continuous agricultural management and the other under beech forest. The CO2 evolution rate was immediately stimulated in the agricultural soil and the respiratory quotient (RQ) decreased from 0.8 to 0.4 mol CO2 evolution rate per mol O2 uptake rate, which was below the theoretically expected value of 0.65 and 0.70 for the degradation of n-hexadecane and palmitic acid, respectively. The microbial response was delayed in the forest soil, but developed better than in the agricultural soil throughout the subsequent 2–4 weeks. Consequently, the respiration rate returned earlier to the initial level for the beech forest soil and the δ13C of respired CO2 and RQ approached values before hydrocarbon addition. Based on the link among respiration rates, RQ and 13C–CO2 value, the added oil-analogue compounds induced a more rapid response in the agricultural soil and were degraded more completely in the forest soil. We concluded that the resilience, which we defined here as the capacity of the soil microbiota to buffer perturbance and to reorganise in response to change resulting in a more desirable system, was higher in our forest soil than for the agricultural soil.

Highlights

► Oil-analogue degradation in soil was monitored on the basis of carbon dioxide evolution and carbon isotopic characteristics. ► Carbon dioxide and oxygen uptake provide complementary information. ► Forest soil was more efficient than agricultural soils.

Introduction

Our global transport system and power generating industry is based on the extraction of fossil hydrocarbon fuels such as crude oil that may contribute to increased concentrations of organic pollutants in the atmosphere, hydrosphere, and geosphere (O’Donoghue and Broderick, 2009, Li and Boufadel, 2010). The combustion of fossil fuels has already led to significant changes in atmospheric carbon dioxide content and signature (Intergovernmental Panel on Climate Change, 2007). In addition, the pollution of soil poses the need for efficient monitoring and control of the fate of the anthropogenic hydrocarbons as they affect sustainability issues such as plant growth (Adam and Duncan, 2002, Adam and Duncan, 2003).

Microbial communities have the unique capability to adjust to unfavourable conditions and to use a broad spectrum of substrates. They have metabolic systems that allow them to utilise both natural and synthetic sources such as exogenous petroleum for energy and tissue constituents. In particular, the n-hexadecane and palmitic acid are constituents of fossil fuels. In natural systems, fatty acids such as palmitic acids are metabolised for NADPH and ATP generation. Fatty acids are esterified to a glycerol backbone to form a group of compounds known as mono-, di-, and tri-glycerides (neutral fats). Energy is released when fatty acids are degraded and also serve as precursors for a number of cell components that are structurally and physiologically essential.

Monitoring of soil hydrocarbon pollution and transformation activity can be done by estimating the concentration of the pollutant and the formation of the respective metabolites. One of the most ubiquitous and universal metabolites is carbon dioxide since respiration is the prominent pathway of biologically processed carbon. When hydrocarbons have carbon isotope characteristics that differ from soil organic components, the 13C–CO2 characteristics can also be used to monitor their mineralisation (Zyakun et al., 2003). Since hydrocarbons require a high amount of oxygen for complete oxidation, the RQ should be affected as well (Dilly, 2001) as oxygen limitation may induce changes in cytochrome levels (Asperger et al., 1986).

The aim of this study is to evaluate the response of soil microbial community to addition of reduced substrates such as n-hexadecane (C16H34) and palmitic acid (C16H32O2) using the CO2 evolution rate, the RQ, and the 13C–CO2 isotopic signature. Additionally, the degradation of palmitic acid was studied due to its primary functions for cell systems. After monitoring the respiratory characteristics, the residual hydrocarbons were estimated. This study should give information on the resilience of soil systems to buffer perturbations and change resulting in a more desirable (here non-polluted) system and also about the soil energetic characteristics, which can be defined as soil energomics (Dilly et al., 2010).

Section snippets

Soil characteristics and sampling

Two soils were sampled at the Bornhöved Lake District in northern Germany (54°06′N, 10°14′E). The first was a soil having a pH [H2O] of 6.4, organic C and total N content of 14.4 mg C and 1.4 mg N g−1 soil, respectively. This agricultural soil, eutri-cambic Arenosol (IUSS Working Group WRB, 2006), was under Lolium perenne grassland since 2003, after regular crop rotation. The second, dystric-cambic Arenosol forest soil (IUSS Working Group WRB, 2006), developed under beech forest under a mature

Basal respiration

The CO2 evolution rate was significantly higher for the agricultural soil than for the forest soil immediately after starting the experiment (Fig. 1). However, the difference in CO2 evolution rate was not significant at 3 days before n-hexadecane addition (Fig. 1) or before palmitic acid addition (Fig. 2). The RQ during basal metabolism was 0.7 and 0.9 mol CO2 mol−1 O2 for the agricultural and the forest soil, respectively (Fig. 1, Fig. 2). The δ13C–CO2 during basal metabolism was −26.7 ± 0.3‰

Discussion

The addition of n-hexadecane and palmitic acid immediately stimulated microbial respiration in both the agricultural and the forest soil. However, the soil microbial communities in the agricultural soil responded more rapidly in comparison to the forest soil. It seems that the microbiota in the agricultural soil seems physiologically better adjusted to n-hexadecane and palmitic acid (Palmroth et al., 2005) and the microbial communities in the forest soil were in a more inactive state compared

Acknowledgement

These studies were financially supported by German Research Foundation, the Ministry for Science, Research and Culture (MWFK) of the Brandenburg state, EFRE and SENSOR. The completion of this work was supported through the Cluster of Excellence ‘Climate System Analysis and Predication – CliSAP’, University of Hamburg, funded through the German Science Foundation (DFG). The authors thank Maria Koon for editing the English.

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