Abstract

Abstract. Transport and reactivity of carbon in the critical zone are highly controlled by reactions of dissolved organic matter (DOM) with subsurface soils, including adsorption, transformation and exchange. These reactions are dependent on frequent wet–dry cycles common to the unsaturated zone, particularly in semi-arid regions. To test for an effect of wet–dry cycles on DOM interaction and stabilization in subsoils, samples were collected from subsurface (Bw) horizons of an Entisol and an Alfisol from the Catalina-Jemez Critical Zone Observatory and sequentially reacted (four batch steps) with DOM extracted from the corresponding soil litter layers. Between each reaction step, soils either were allowed to air dry (wet–dry treatment) before introduction of the following DOM solution or were maintained under constant wetness (continually wet treatment). Microbial degradation was the dominant mechanism of DOM loss from solution for the Entisol subsoil, which had higher initial organic C content, whereas sorptive retention predominated in the lower C Alfisol subsoil. For a given soil, bulk dissolved organic C losses from solution were similar across treatments. However, a combination of Fourier transform infrared (FTIR) and near-edge X-ray absorption fine structure (NEXAFS) spectroscopic analyses revealed that wet–dry treatments enhanced the interactions between carboxyl functional groups and soil particle surfaces. Scanning transmission X-ray microscopy (STXM) data suggested that cation bridging by Ca2+ was the primary mechanism for carboxyl association with soil surfaces. STXM data also showed that spatial fractionation of adsorbed OM on soil organo-mineral surfaces was diminished relative to what might be inferred from previously published observations pertaining to DOM fractionation on reaction with specimen mineral phases. This study provides direct evidence of the role of wet–dry cycles in affecting sorption reactions of DOM to a complex soil matrix. In the soil environment, where wet–dry cycles occur at different frequencies from site to site and along the soil profile, different interactions between DOM and soil surfaces are expected and need to be considered for the overall assessment of carbon dynamics.

Highlights

  • Dissolved organic matter (DOM) is the main vehicle of organic carbon (OC) and nutrient transport to the subsoil (Kaiser and Kalbitz, 2012; Kalbitz et al, 2000)

  • The mean fraction of OC removed from DOM solution was 58 ± 5 % (SD) after each reaction step with Jemez River Basin (JRB) soil, and OC uptake values were not significantly different between the continuously wet and wet–dry treatments

  • At the end of four reaction steps the Total organic carbon (TOC) of JRB soils increased from 1700 ± 74 mg OC kg−1 for the unreacted soil to 2750 ± 87 and 2840 ± 99 mg OC kg−1 for the wet–dry and continuously wet treatments, respectively (Fig. 1)

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Summary

Introduction

Dissolved organic matter (DOM) is the main vehicle of organic carbon (OC) and nutrient transport to the subsoil (Kaiser and Kalbitz, 2012; Kalbitz et al, 2000). There it stimulates key biogeochemical processes including heterotrophic microbial activity (Fontaine et al, 2007), mineral transformation and organic and inorganic nutrient and contaminant mobilization (Chorover et al, 2007; Polubesova and Chefetz, 2014; Zhao et al, 2011). Such cyclic conditions likely impact C dynamics, the nature of their effects on micro- to molecular-scale organo-mineral associations remains poorly known

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