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Geology topics

Jennifer L. Druhan

Publications and source records attributed to Jennifer L. Druhan.

2 recordsLinked to original sources

Deep root activity overprints weathering of petrogenic organic carbon in shale

The oxidation of organic carbon in sedimentary bedrock (petrogenic OC, OC p e t r o "> petro ) is increasingly recognized as a potential source of CO 2 to the atmosphere. Recent studies provide evidence for the mobilization and oxidation of OC p e t r o "> petro in sedimentary bedrock during rock weathering. However, the mechanisms and rates remain uncertain, particularly where overlying soils and vegetation drive contemporaneous oxidation of recently fixed organic carbon. Here, we quantify OC p e t r o "> petro weathering across a 16 m shale depth profile in a steep, rapidly eroding forested hillslope in the Northern California Coast Ranges. We report solid and gas phase radiocarbon and stable isotope analyses of samples extracted from specialized in-situ samplers, and a supporting laboratory incubation experiment of the shale regolith. OC p e t r o "> petro is removed from the weathered bedrock at a rate of approximately 0.12 gC/m 3 yr, which is orders of magnitude lower than the rate of OC p e t r o "> petro oxidation we achieved in the laboratory with crushed samples (557.1 gC/m 3 /yr). This disparity occurs despite high O 2 ( g ) "> 2(g) content across the depth profile, indicating that physical accessibility of OC p e t r o "> petro can regulate oxidative weathering. There is no direct radiocarbon evidence of OC p e t r o "> petro oxidation in CO 2 ( g ) "> 2(g) across the upper 13 m of the weathering profile during both wet and dry seasons. Instead, vadose zone CO 2 ( g ) "> 2(g) production at the site is dominated by respiration of recently fixed carbon associated with deep rooting. OC p e t r o "> petro is clearly mobilized across the vadose zone during weathering in this rapidly eroding, oxygen-rich, biologically dynamic hillslope, but at rates far below what can be measured given the contribution of root-derived CO 2 ( g ) "> 2(g) .

California

Improving understanding of soil organic matter dynamics by triangulating theories, measurements, and models

Soil organic matter (SOM) turnover increasingly is conceptualized as a tension between accessibility to microorganisms and protection from decomposition via physical and chemical association with minerals in emerging soil biogeochemical theory. Yet, these components are missing from the original mathematical models of belowground carbon dynamics and remain underrepresented in more recent compartmental models that separate SOM into discrete pools with differing turnover times. Thus, a gap currently exists between the emergent understanding of SOM dynamics and our ability to improve terrestrial biogeochemical projections that rely on the existing models. In this opinion paper, we portray the SOM paradigm as a triangle composed of three nodes: conceptual theory, analytical measurement, and numerical models. In successful approaches, we contend that the nodes are connected—models capture the essential features of dominant theories while measurement tools generate data adequate to parameterize and evaluate the models—and balanced—models can inspire new theories via emergent behaviors, pushing empiricists to come up with new measurements. Many exciting advances recently pushed the boundaries on one or more nodes. However, newly integrated triangles have yet to coalesce. We conclude that our ability to incorporate mechanisms of microbial decomposition and physicochemical protection into predictions of SOM change is limited by current disconnections and imbalances among theory, measurement, and modeling. Opportunities to reintegrate the three components of the SOM paradigm exist by carefully considering their linkages and feedbacks at specific scales of observation.

Biogeochemistry