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Susan E. Trumbore

Bio: Susan E. Trumbore is an academic researcher from Max Planck Society. The author has contributed to research in topics: Soil carbon & Soil water. The author has an hindex of 95, co-authored 337 publications receiving 34844 citations. Previous affiliations of Susan E. Trumbore include Columbia University & Lawrence Livermore National Laboratory.


Papers
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Journal ArticleDOI
06 Oct 2011-Nature
TL;DR: In this article, a new generation of experiments and soil carbon models were proposed to predict the SOM response to global warming, and they showed that molecular structure alone alone does not control SOM stability.
Abstract: Globally, soil organic matter (SOM) contains more than three times as much carbon as either the atmosphere or terrestrial vegetation. Yet it remains largely unknown why some SOM persists for millennia whereas other SOM decomposes readily—and this limits our ability to predict how soils will respond to climate change. Recent analytical and experimental advances have demonstrated that molecular structure alone does not control SOM stability: in fact, environmental and biological controls predominate. Here we propose ways to include this understanding in a new generation of experiments and soil carbon models, thereby improving predictions of the SOM response to global warming.

4,219 citations

Journal ArticleDOI
01 Jan 1997-Nature
TL;DR: In this article, the authors explore the relationship between soil mineralogy and organic carbon along two natural gradients (i.e., soil-age and climate) in volcanic soil environments.
Abstract: A large source of uncertainty in present understanding of the global carbon cycle is the distribution and dynamics of the soil organic carbon reservoir. Most of the organic carbon in soils is degraded to inorganic forms slowly, on timescales from centuries to millennia1. Soil minerals are known to play a stabilizing role, but how spatial and temporal variation in soil mineralogy controls the quantity and turnover of long-residence-time organic carbon is not well known2. Here we use radiocarbon analyses to explore interactions between soil mineralogy and soil organic carbon along two natural gradients—of soil-age and of climate—in volcanic soil environments. During the first ∼150,000 years of soil development, the volcanic parent material weathered to metastable, non-crystalline minerals. Thereafter, the amount of non-crystalline minerals declined, and more stable crystalline minerals accumulated. Soil organic carbon content followed a similar trend, accumulating to a maximum after 150,000 years, and then decreasing by 50% over the next four million years. A positive relationship between non-crystalline minerals and organic carbon was also observed in soils through the climate gradient, indicating that the accumulation and subsequent loss of organic matter were largely driven by changes in the millennial scale cycling of mineral-stabilized carbon, rather than by changes in the amount of fast-cycling organic matter or in net primary productivity. Soil mineralogy is therefore important in determining the quantity of organic carbon stored in soil, its turnover time, and atmosphere–ecosystem carbon fluxes during long-term soil development; this conclusion should be generalizable at least to other humid environments.

1,308 citations

Journal ArticleDOI
01 Dec 1994-Nature
TL;DR: In this article, the authors estimate that half of the closed forests of Brazilian Amazonia depend on deep root systems to maintain green canopies during the dry season, and as much as 15% of this deep-soil carbon turns over on annual or decadal timescales.
Abstract: DEFORESTATION and logging transform more forest in eastern and southern Amazonia than in any other region of the world1–3. This forest alteration affects regional hydrology4–11 and the global carbon cycle12–14, but current analyses of these effects neglect an important deep-soil link between the water and carbon cycles. Using rainfall data, satellite imagery and field studies, we estimate here that half of the closed forests of Brazilian Amazonia depend on deep root systems to maintain green canopies during the dry season. Evergreen forests in northeastern Para state maintain evapotranspiration during five-month dry periods by absorbing water from the soil to depths of more than 8m. In contrast, although the degraded pastures of this region also contain deep-rooted woody plants, most pasture plants substantially reduce their leaf canopy in response to seasonal drought, thus reducing dry-season evapotranspiration and increasing potential subsurface runoff relative to the forests they replace. Deep roots that extract water also provide carbon to the soil. The forest soil below 1 m depth contains more carbon than does above-ground biomass, and as much as 15% of this deep-soil carbon turns over on annual or decadal timescales. Thus, forest alteration that affects depth distributions of carbon inputs from roots may also affect net carbon storage in the soil.

1,288 citations

Journal ArticleDOI
TL;DR: In this article, the authors used radiocarbon data from soil organic matter and soil respiration to determine carbon dynamics and thereby the magnitude and timing of the soil carbon response to global change.
Abstract: Radiocarbon data from soil organic matter and soil respiration provide pow- erful constraints for determining carbon dynamics and thereby the magnitude and timing of soil carbon response to global change. In this paper, data from three sites representing well-drained soils in boreal, temperate, and tropical forests are used to illustrate the methods for using radiocarbon to determine the turnover times of soil organic matter and to partition soil respiration. For these sites, the average age of bulk carbon in detrital and Oh/A-horizon organic carbon ranges from 200 to 1200 yr. In each case, this mass-weighted average includes components such as relatively undecomposed leaf, root, and moss litter with much shorter turnover times, and humified or mineral-associated organic matter with much longer turnover times. The average age of carbon in organic matter is greater than the average age predicted for CO2 produced by its decomposition (30, 8, and 3 yr for boreal, temperate, and tropical soil), or measured in total soil respiration (16, 3, and 1 yr). Most of the CO 2 produced during decomposition is derived from relatively short-lived soil organic matter (SOM) components that do not represent a large component of the standing stock of soil organic matter. Estimates of soil carbon turnover obtained by dividing C stocks by hetero- trophic respiration fluxes, or from radiocarbon measurements of bulk SOM, are biased to longer time scales of C cycling. Failure to account for the heterogeneity of soil organic matter will result in underestimation of the short-term response and overestimation of the long-term response of soil C storage to future changes in inputs or decomposition. Comparison of the 14 C in soil respiration with soil organic matter in temperate and boreal forest sites indicates a significant contribution from decomposition of organic matter fixed.2 yr but ,30 yr ago. Tropical soil respiration is dominated by C fixed ,1 yr ago. Monitoring the 14 C signature of CO2 emitted from soils give clues as to the causes of

985 citations

Journal ArticleDOI
TL;DR: It is shown that higher plant diversity increases rhizosphere carbon inputs into the microbial community resulting in both increased microbial activity and carbon storage, indicating that the increase in carbon storage is mainly limited by the integration of new carbon into soil and less by the decomposition of existing soil carbon.
Abstract: Plant diversity strongly influences ecosystem functions and services, such as soil carbon storage. However, the mechanisms underlying the positive plant diversity effects on soil carbon storage are poorly understood. We explored this relationship using long-term data from a grassland biodiversity experiment (The Jena Experiment) and radiocarbon ((14)C) modelling. Here we show that higher plant diversity increases rhizosphere carbon inputs into the microbial community resulting in both increased microbial activity and carbon storage. Increases in soil carbon were related to the enhanced accumulation of recently fixed carbon in high-diversity plots, while plant diversity had less pronounced effects on the decomposition rate of existing carbon. The present study shows that elevated carbon storage at high plant diversity is a direct function of the soil microbial community, indicating that the increase in carbon storage is mainly limited by the integration of new carbon into soil and less by the decomposition of existing soil carbon.

891 citations


Cited by
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Journal ArticleDOI
TL;DR: In this paper, Heaton, AG Hogg, KA Hughen, KF Kaiser, B Kromer, SW Manning, RW Reimer, DA Richards, JR Southon, S Talamo, CSM Turney, J van der Plicht, CE Weyhenmeyer
Abstract: Additional co-authors: TJ Heaton, AG Hogg, KA Hughen, KF Kaiser, B Kromer, SW Manning, RW Reimer, DA Richards, JR Southon, S Talamo, CSM Turney, J van der Plicht, CE Weyhenmeyer

13,605 citations

Journal ArticleDOI
09 Mar 2006-Nature
TL;DR: This work has suggested that several environmental constraints obscure the intrinsic temperature sensitivity of substrate decomposition, causing lower observed ‘apparent’ temperature sensitivity, and these constraints may, themselves, be sensitive to climate.
Abstract: Significantly more carbon is stored in the world's soils--including peatlands, wetlands and permafrost--than is present in the atmosphere. Disagreement exists, however, regarding the effects of climate change on global soil carbon stocks. If carbon stored belowground is transferred to the atmosphere by a warming-induced acceleration of its decomposition, a positive feedback to climate change would occur. Conversely, if increases of plant-derived carbon inputs to soils exceed increases in decomposition, the feedback would be negative. Despite much research, a consensus has not yet emerged on the temperature sensitivity of soil carbon decomposition. Unravelling the feedback effect is particularly difficult, because the diverse soil organic compounds exhibit a wide range of kinetic properties, which determine the intrinsic temperature sensitivity of their decomposition. Moreover, several environmental constraints obscure the intrinsic temperature sensitivity of substrate decomposition, causing lower observed 'apparent' temperature sensitivity, and these constraints may, themselves, be sensitive to climate.

5,367 citations

Journal ArticleDOI
TL;DR: The use of stable isotopes to solve biogeochemical problems in ecosystem analysis is increasing rapidly because stable isotope data can contribute both source-sink (tracer) and process information: the elements C, N, S, H, and all have more than one isotope, and isotopic compositions of natural materials can be measured with great precision with a mass spectrometer as mentioned in this paper.
Abstract: The use of stable isotopes to solve biogeochemical problems in ecosystem analysis is increasing rapidly because stable isotope data can contribute both source-sink (tracer) and process information: The elements C, N, S, H, and all have more than one isotope, and isotopic compositions of natural materials can be measured with great precision with a mass spectrometer. Isotopic compositions change in predictable ways as elements cycle through the biosphere. These changes have been exploited by geochemists to understand the global elemental cycles. Ecologists have not until quite recently employed these techniques. The reasons for this are, first, that most ecologists do not have the background in chemistry and geochemistry to be fully aware of the possibilities for exploiting the natural variations in stable isotopic compositions, and second, that stable isotope ratio measurements require equipment not normally available to ecologists. This is unfortunate because some of the more intractable problems in ecology can be profitably addressed using stable isotope measurements. Stable isotopes are ideally suited to increase our understanding of element cycles in ecosystems. This review is written for ecologists who would like to learn more about how stable isotope analyses have been and can be used in ecosystem studies. We begin with an explanation of isotope terminology and fractionation, then summarize isotopic distributions in the C, N, and S biogeochemical cycles, and conclude with five case studies that show how stable isotope measurements can provide crucial information for ecosystem analysis. We restrict this review to studies of natural variations in C, N, and S isotopic abundances, cxcluding from consideration ~5N enrichment studies and hydrogen and oxygen isotope studies. Our focus on C, N, and S derives in part from our

5,234 citations

Journal ArticleDOI
01 Dec 1989-Nature
TL;DR: In this paper, a global oxygen isotope record for ocean water has been calculated from the Barbados sea level curve, allowing separation of the ice volume component common to all isotope records measured in deep-sea cores.
Abstract: Coral reefs drilled offshore of Barbados provide the first continuous and detailed record of sea level change during the last deglaciation. The sea level was 121 ± 5 metres below present level during the last glacial maximum. The deglacial sea level rise was not monotonic; rather, it was marked by two intervals of rapid rise. Varying rates of melt-water discharge to the North Atlantic surface ocean dramatically affected North Atlantic deep-water production and oceanic oxygen isotope chemistry. A global oxygen isotope record for ocean water has been calculated from the Barbados sea level curve, allowing separation of the ice volume component common to all oxygen isotope records measured in deep-sea cores.

4,483 citations