Geology topics

Asmeret Asefaw Berhe

Publications and source records attributed to Asmeret Asefaw Berhe.

7 recordsLinked to original sources

USGS2025

A landscape-scale view of soil organic matter dynamics

Soil carbon is an important component of the terrestrial carbon cycle and could be augmented through improved soil management to mitigate climate change. However, data gaps for numerous regions and a lack of understanding of the heterogeneity of biogeochemical processes across diverse soil landscapes hinder the development of large-scale representations of soil organic matter (SOM) dynamics. In this Perspective, we outline how understanding soil formation processes and complexity at the landscape scale can inform predictions of soil organic matter (SOM) cycling and soil carbon sequestration. Long-term alterations of the soil matrix caused by weathering and soil redistribution vary across climate zones and ecosystems, but particularly with the structure of landscapes at the regional scale. Thus, oversimplified generalizations that assume that the drivers of SOM dynamics can be scaled directly from local to global regimes and vice versa leads to large uncertainties in global projections of soil C stocks. Data-driven models with enhanced coverage of underrepresented regions, particularly where soils are physicochemically distinct and environmental change is most rapid, are key to understanding C turnover and stabilization at landscape scales to better predict global soil carbon dynamics.

Nature Reviews Earth & Environment↗

USGS2021

Beyond bulk: Density fractions explain heterogeneity in global soil carbon abundance and persistence

Understanding the controls on the amount and persistence of soil organic carbon (C) is essential for predicting its sensitivity to global change. The response may depend on whether C is unprotected, isolated within aggregates, or protected from decomposition by mineral associations. Here, we present a global synthesis of the relative influence of environmental factors on soil organic C partitioning among pools, abundance in each pool (mg C g −1 soil), and persistence (as approximated by radiocarbon abundance) in relatively unprotected particulate and protected mineral-bound pools. We show that C within particulate and mineral-associated pools consistently differed from one another in degree of persistence and relationship to environmental factors. Soil depth was the best predictor of C abundance and persistence, though it accounted for more variance in persistence. Persistence of all C pools decreased with increasing mean annual temperature (MAT) throughout the soil profile, whereas persistence increased with increasing wetness index (MAP/PET) in subsurface soils (30–176 cm). The relationship of C abundance (mg C g −1 soil) to climate varied among pools and with depth. Mineral-associated C in surface soils (<30 cm) increased more strongly with increasing wetness index than the free particulate C, but both pools showed attenuated responses to the wetness index at depth. Overall, these relationships suggest a strong influence of climate on soil C properties, and a potential loss of soil C from protected pools in areas with decreasing wetness. Relative persistence and abundance of C pools varied significantly among land cover types and soil parent material lithologies. This variability in each pool's relationship to environmental factors suggests that not all soil organic C is equally vulnerable to global change. Therefore, projections of future soil organic C based on patterns and responses of bulk soil organic C may be misleading.

Global Change Biology↗

USGS2019

Global ecological predictors of the soil priming effect

Identifying the global drivers of soil priming is essential to understanding C cycling in terrestrial ecosystems. We conducted a survey of soils across 86 globally-distributed locations, spanning a wide range of climates, biotic communities, and soil conditions, and evaluated the apparent soil priming effect using 13 C-glucose labeling. Here we show that the magnitude of the positive apparent priming effect (increase in CO 2 release through accelerated microbial biomass turnover) was negatively associated with SOC content and microbial respiration rates. Our statistical modeling suggests that apparent priming effects tend to be negative in more mesic sites associated with higher SOC contents. In contrast, a single-input of labile C causes positive apparent priming effects in more arid locations with low SOC contents. Our results provide solid evidence that SOC content plays a critical role in regulating apparent priming effects, with important implications for the improvement of C cycling models under global change scenarios.

Nature Communications↗

USGS2018

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↗

USGS2018

Beyond clay: Towards an improved set of variables for predicting soil organic matter content

Improved quantification of the factors controlling soil organic matter (SOM) stabilization at continental to global scales is needed to inform projections of the largest actively cycling terrestrial carbon pool on Earth, and its response to environmental change. Biogeochemical models rely almost exclusively on clay content to modify rates of SOM turnover and fluxes of climate-active CO 2 to the atmosphere. Emerging conceptual understanding, however, suggests other soil physicochemical properties may predict SOM stabilization better than clay content. We addressed this discrepancy by synthesizing data from over 5,500 soil profiles spanning continental scale environmental gradients. Here, we demonstrate that other physicochemical parameters are much stronger predictors of SOM content, with clay content having relatively little explanatory power. We show that exchangeable calcium strongly predicted SOM content in water-limited, alkaline soils, whereas with increasing moisture availability and acidity, iron- and aluminum-oxyhydroxides emerged as better predictors, demonstrating that the relative importance of SOM stabilization mechanisms scales with climate and acidity. These results highlight the urgent need to modify biogeochemical models to better reflect the role of soil physicochemical properties in SOM cycling.

Biogeochemistry↗

USGS2012

Persistence of soil organic matter in eroding versus depositional landform positions

Soil organic matter (SOM) processes in dynamic landscapes are strongly influenced by soil erosion and sedimentation. We determined the contribution of physical isolation of organic matter (OM) inside aggregates, chemical interaction of OM with soil minerals, and molecular structure of SOM in controlling storage and persistence of SOM in different types of eroding and depositional landform positions. By combining density fractionation with elemental and spectroscopic analyses, we showed that SOM in depositional settings is less transformed and better preserved than SOM in eroding landform positions. However, which environmental factors exert primary control on storage and persistence of SOM depended on the nature of the landform position considered. In an annual grassland watershed, protection of SOM by physical isolation inside aggregates and chemical association of organic matter (complexation) with soil minerals, as assessed by correlation with radiocarbon concentration, were more effective in the poorly drained, lowest-lying depositional landform positions, compared to well-drained landform positions in the upper parts of the watershed. Results of this study demonstrated that processes of soil erosion and deposition are important mechanisms of long-term OM stabilization.

Journal of Geophysical Research: Biogeosciences↗

USGS2008

Linking soil organic matter dynamics and erosion-induced terrestrial carbon sequestration at different landform positions

Recently, the potential for terrestrial carbon (C) sequestration by soil erosion and deposition has received increased interest. Erosion and deposition constitute a sink for atmospheric carbon dioxide relative to a preerosional state or a noneroding scenario, if the posterosion watershed C balance is increased due to (1) partial replacement of eroded C by new photosynthate in the eroded site; and (2) preservation from decomposition of at least some eroded soil organic carbon (SOC) arriving in depositional settings. Little is known, however, about differences in C dynamics at different erosional and depositional landform positions within the same eroding system. We determined the contribution of different landform positions to erosion-induced terrestrial C sequestration by measuring rates of net primary productivity (NPP), replacement of eroded C, and decomposition of organic matter (OM) at four categorically different landform positions within a naturally eroding toposequence in northern California. We found that eroded C is replaced by NPP 15 times over in the summit of the site studied and 5 times over in the slope. Profile-averaged, long-term rate constant for SOM decomposition was 2 to 14 times slower in the depositional settings compared with that in eroding slopes. As a result, the inventory of C in the depositional settings was 2 to 3 times larger than that of the eroding positions. Owing to both C replacement at eroding sites and reduced rates of OM decomposition in depositional sites, soil erosion constitutes a C sink from the atmosphere at our study site.

California↗