Abstract. In contrast to mineral topsoils, in subsoils the origin and processes leading to the formation and stabilization of organic matter (OM) are still not well known. This study addresses the fate of litter-derived carbon (C) in whole soil profiles with regard to the conceptual cascade model, which proposes that OM formation in subsoils is linked to sorption–microbial processing–remobilization cycles during the downward migration of dissolved organic carbon (DOC). Our main objectives were to quantify the contribution of recent litter to subsoil C stocks via DOC translocation and to evaluate the stability of litter-derived OM in different functional OM fractions. A plot-scale stable isotope-labeling experiment was conducted in a temperate beech forest by replacing the natural litter layer with 13C enriched litter on an area of 20 m2 above a Dystric Cambisol. After 22 months of field exposure, the labeled litter was replaced again by natural litter and soil cores were drilled down to 180 cm soil depth. Water extraction and density fractionation were combined with stable isotope measurements in order to link the fluxes of recent litter-derived C to its allocation into different functional OM fractions. A second sampling was conducted 18 months later to further account for the stability of translocated young litter-derived C. Almost no litter-derived particulate OM (POM) entered the subsoil, suggesting root biomass as the major source of subsoil POM. The contribution of aboveground litter to the formation of mineral-associated OM (MAOM) in topsoils (0–10 cm) was 1.88±0.83 g C m−2 and decreased to 0.69±0.19 g C m−2 in the upper subsoil (10–50 cm) and 0.01±0.02 g C m−2 in the deep subsoil >100 cm soil depth during the 22 months. This finding suggests a subordinate importance of recent litter layer inputs via DOC translocation to subsoil C stocks, and implies that most of the OM in the subsoil is of older age. Smaller losses of litter-derived C within MAOM of about 66 % compared to POM (77 %–89 %) over 18 months indicate that recent carbon can be stabilized by interaction with mineral surfaces; although the overall stabilization in the sandy study soils is limited. Our isotope-labeling approach supports the concept of OM undergoing a sequence of cycles of sorption, microbial processing, and desorption while migrating down a soil profile, which needs to be considered in models of soil OM formation and subsoil C cycling.

Abstract. In contrast to mineral topsoils, the origin and processes leading to the formation and stabilization of organic matter (OM) in subsoils is still not well known. This study addresses the fate of litter-derived carbon (C) in whole soil profiles with regard to the conceptual cascade model, which proposes that OM formation in subsoils is linked to sorption-microbial processing-remobilization cycles during the downward migration of dissolved organic carbon (DOC). Our main objectives were to quantify the contribution of recent litter to subsoil C stocks via DOC movement and to evaluate the stability of litter-derived OM in different functional OM fractions. A plot-scale stable isotope labeling experiment was conducted in a temperate beech forest by replacing the natural litter layer with 13C enriched litter on an area of 20 m2 above a Dystric Cambisol. After 22 months of field exposure, the labeled litter was replaced again by natural litter and soil cores were drilled down to 180 cm soil depth. Water extraction and density fractionation were combined with stable isotope measurements in order to link the fluxes of recent litter-derived C to its allocation into different functional OM fractions. A second sampling was conducted 18 months later to further account for the stability of translocated young litter-derived C. Almost no litter-derived particulate OM (POM) entered the subsoil, suggesting root biomass as the major source of subsoil POM. The contribution of aboveground litter to the formation of mineral-associated OM (MAOM) in topsoils (0–10 cm) was 0.99 ± 0.45 g C m−2 yr−1, and decreased to 0.37 ± 0.10 g C m−2 yr−1 in the upper subsoil (10–50 cm) and 0.01 ± 0.01 g C m−2 yr−1 in the deep subsoil > 100 cm soil depth. This finding suggests a subordinate importance of recent litter layer inputs via DOC translocation to subsoil C stocks, and implies that most of the OM in the subsoil is of older age. Smaller losses of litter-derived C within MAOM of about 66 % compared to POM (77–89 %) indicate that recent carbon can be stabilized by interaction with mineral surfaces; although the overall stabilization in the sandy study soils was low. Our isotope labeling approach supports the concept of OM undergoing a sequence of cycles of sorption, microbial processing, and desorption while migrating down a soil profile, which needs to be considered in models on soil OM formation and subsoil C cycling.

Dissolved organic carbon (DOC) from Oa horizons has been proposed to be an important contributor for subsoil organic carbon stocks. We investigated the fate of DOC by directly injecting a DOC solution from 13 C labelled litter into three soil depths at beech forest sites. Fate of injected DOC was quantified with deep drilling soil cores down to 2 m depth, 3 and 17 months after the injection. 27 ± 26% of the injected DOC was retained after 3 months and 17 ± 22% after 17 months. Retained DOC was to 70% found in the first 10 cm below the injection depth and on average higher in the topsoil than in the subsoil. After 17 months DOC in the topsoil was largely lost (-19%) while DOC in the subsoil did not change much (-4.4%). Data indicated a high stabilisation of injected DOC in the subsoils with no differences between the sites. Potential mineralisation as revealed by incubation experiments however, was not different between DOC injected in topsoil or subsoils underlining the importance of environmental factors in the subsoil for DOC stabilisation compared to topsoil. We conclude that stability of DOC in subsoil is primary driven by its spatial inaccessibility for microorganisms after matrix flow while site specific properties did not significantly affect stabilisation. Instead, a more fine-textured site promotes the vertical transport of DOC due to a higher abundance of preferential flow paths.

Abstract. Geogenic organic carbon (GOC) from sedimentary rocks is an overlooked fraction in soils that has not yet been quantified but influences the composition, age, and stability of total organic carbon (OC) in soils. In this context, GOC is the OC in bedrock deposited during sedimentation. The contribution of GOC to total soil OC may vary, depending on the type of bedrock. However, no studies have been carried out to investigate the contribution of GOC derived from different terrestrial sedimentary rocks to soil OC contents. In order to fill this knowledge gap, 10 m long sediment cores from three sites recovered from Pleistocene loess, Miocene sand, and Triassic Red Sandstone were analysed at 1 m depth intervals, and the amount of GOC was calculated based on 14C measurements. The 14C ages of bulk sedimentary OC revealed that OC is comprised of both biogenic and geogenic components. The biogenic component relates to OC that entered the sediments from plant sources since soil development started. Assuming an average age for this biogenic component ranging from 1000–4000 years BP (before present), we calculated average amounts of GOC in the sediments starting at 1.5 m depth, based on measured 14C ages. The median amount of GOC in the sediments was then taken, and its proportion of soil mass (g GOC per kg−1 fine soil) was calculated in the soil profile. All the sediments contained considerable amounts of GOC (median amounts of 0.10 g kg−1 in Miocene sand, 0.27 g kg−1 in Pleistocene loess, and 0.17 g kg−1 in Red Sandstone) compared with subsoil OC contents (between 0.53 and 15.21 g kg−1). Long-term incubation experiments revealed that the GOC appeared comparatively stable against biodegradation. Its possible contribution to subsoil OC stocks (0.3–1.5 m depth) ranged from 1 % to 26 % in soil developed in the Miocene sand, from 16 % to 21 % in the loess soil, and from 6 % to 36 % at the Red Sandstone site. Thus, GOC with no detectable 14C content influenced the 14C ages of subsoil OC and may partly explain the strong increase in 14C ages observed in many subsoils. This could be particularly important in young soils on terrestrial sediments with comparatively low amounts of OC, where GOC can make a large contribution to total OC stocks.

Abstract. Geogenic organic carbon (GOC) from sedimentary rocks is an overlooked fraction in soils that has not been quantified yet, influencing the composition, age and stability of total organic carbon (OC) in soils. In this context GOC is referred to as the OC in bedrocks deposited during sedimentation. However, the contribution of GOC to total soil OC varies with the type of bedrock. So far studies investigating the contribution of GOC derived from different terrestrial sedimentary rocks to soil OC contents are missing. In order to fill this gap, we analysed 10 m long sediment cores at three sites recovered from Pleistocene Loess, Miocene Sand and Triassic Red Sandstone and calculated the amount of GOC based on 14C measurements. 14C ages of bulk sedimentary OC revealed that OC represents a mixture of biogenic and geogenic components. Biogenic refers to OC that entered the sediments recently from plant sources. All sediments contain considerable amounts of GOC (median amounts of 0.10 g kg−1 at the Miocene Sand, 0.27 g kg−1 at the Pleistocene Loess and 0.17 at Red Sandstone) in comparison to subsoil OC contents (between 0.53–15.21 g kg−1). Long-term incubation experiments revealed that this GOC seemed to be comparatively stable against biodegradation. Its possible contribution to subsoil OC stocks (0.3–1.5 m depth) is ~ 2.5 % in soil developed in the Miocene Sand, ~ 8 % in the Loess soil and ~ 12 % at the Red Sandstone site. Thus GOC having no detectable 14C contents influences 14C ages of subsoil OC and thus may partly explain the strong 14C ages increase observed in many subsoils. This is particularly important in soils on terrestrial sediments with comparatively low amounts of OC, where GOC can considerably contribute to total OC stocks.