The impact of land use change on C turnover in soils

Measurements of CO2 flux, soil temperature, and moisture content of selected natural and disturbed soils in central California were made on a monthly basis from August 1994 to October 1995 in an attempt to detect the effects of temperature, moisture, and land use change on CO2 production in soils. Soil CO2 flux displayed a strong negative correlation with soil temperature and a positive correlation with soil moisture at the natural site. However, at the disturbed site, the linear correlation between CO2 flux and temperature/moisture was insignificant. The negative correlation between soil CO2 flux and soil temperature is in contrast to what has been observed in other ecosystems but is typical for Mediterranean ecosystems in which grasses are biologically active only during cool months. Comparison of carbon (C) inventories of paired natural and disturbed soils indicates that both cultivation and logging have resulted in a significant decrease in total soil C content. The reduction in soil C storage is about 26% for the cultivated soil and around 30% for the logged soil. Most of the C loss is from the upper horizons. Radiocarbon (C-14) measurements of both recent and archived soil samples demonstrate large differences in C input rate and turnover time between natural and disturbed soils. The average turnover times of organic matter are longer in disturbed soils than in the corresponding natural soils as a result of preferential loss of C from "active" soil C pools. In both natural and disturbed soils, the average turnover times of organic matter increase with depth from decades or less in shallow horizons to hundreds of years or even thousands of years in deeper horizons. Our results show that land use change can have significant impact on soil C cycle and that shallow soil horizons are most susceptible to disturbance because of shorter turnover times of organic C in these horizons

Models of soil organic matter decomposition: the SOILR package, version 1.0

Soil organic matter decomposition is a very important process within the Earth system because it controls the rates of mineralization of carbon and other biogeochemical elements, determining their flux to the atmosphere and the hydrosphere. SOILR is a modeling framework that contains a library of functions and tools for modeling soil organic matter decomposition under the R environment for computing. It implements a variety of model structures and tools to represent carbon storage and release from soil organic matter. In SOILR, organic matter decomposition is represented as a linear system of ordinary differential equations that generalizes the structure of most compartment-based decomposition models. A variety of functions is also available to represent environmental effects on decomposition rates. This document presents the conceptual basis for the functions implemented in the package. It is complementary to the help pages released with the software

Simultaneous real-time measurement of isoprene and 2-methyl-3-buten-2-ol emissions from trees using SIFT-MS

The C5 hemiterpenes isoprene and 2-methyl-3-buten-2-ol (MBO) are important biogenic volatiles emitted from terrestrial vegetation. Isoprene is emitted from many plant groups, especially trees such as Populus, while emission of MBO is restricted to certain North American conifers, including species of Pinus. MBO is also a pheromone emitted by several conifer bark beetles. Both isoprene and MBO have typically been measured by proton-transfer reaction mass spectrometry (PTR-MS), but this method cannot accurately distinguish between them because of their signal overlap. Our study developed a method for using selective ion flow tube mass spectrometry (SIFT-MS) that allows simultaneous on-line measurement of isoprene and MBO by employing different reagent ions. The use of m/z(NO+) = 68 u for isoprene and m/z(O2 +) = 71 u for MBO gave minimal interference between the compounds. We tested the suitability of the method by measuring the emission of young trees of Populus, Picea, and Pinus. Our results largely confirm previous findings that Populus nigra, Picea glauca, and Picea abies emit isoprene and Pinus ponderosa emits MBO, but we also found MBO to be emitted by Picea abies. Thus SIFT-MS provides a reliable, easy to use, on-line measuring tool to distinguish between isoprene and MBO. The method should be of use to atmospheric chemists, tree physiologists and forest entomologists, among others

Anomalous AMS radiocarbon ages for foraminifera from high-deposition-rate ocean sediments

Radiocarbon ages on handpicked foraminifera from deep-sea cores are revealing that areas of rapid sediment accumulation are in some cases subject to hiatuses, reworking and perhaps secondary calcite deposition. We present here an extreme example of the impacts of such disturbances. The message is that if precise chronologies or meaningful benthic planktic age differences are to be obtained, then it is essential to document the reliability of radiocarbon ages by making both comparisons between coexisting species of planktomc foraminifera and detailed down-core sequences of measurements

How well does ramped thermal oxidation quantify the age distribution of soil carbon? Assessing thermal stability of physically and chemically fractionated soil organic matter

Carbon (C) in soils persists on a range of timescales depending on physical, chemical, and biological processes that interact with soil organic matter (SOM) and affect its rate of decomposition. Together these processes determine the age distribution of soil C. Most attempts to measure this age distribution have relied on operationally defined fractions using properties like density, aggregate stability, solubility, or chemical reactivity. Recently, thermal fractionation, which relies on the activation energy needed to combust SOM, has shown promise for separating young from old C by applying increasing heat to decompose SOM. Here, we investigated radiocarbon (C-14) and C-13 of C released during thermal fractionation to link activation energy to the age distribution of C in bulk soil and components previously separated by density and chemical properties. While physically and chemically isolated fractions had very distinct mean C-14 values, they contributed C across the full temperature range during thermal analysis. Thus, each thermal fraction collected during combustion of bulk soil integrates contributions from younger and older C derived from components having different physical and chemical properties but the same activation energy. Bulk soil and all density and chemical fractions released progressively older and more C-13-enriched C with increasing activation energy, indicating that each operationally defined fraction itself was not homogeneous but contained a mix of C with different ages and degrees of microbial processing. Overall, we found that defining the full age distribution of C in bulk soil is best quantified by first separating particulate C prior to thermal fractionation of mineral-associated SOM. For the Podzol analyzed here, thermal fractions confirmed that similar to 95 % of the mineral-associated organic matter (MOM) had a relatively narrow C-14 distribution, while 5 % was very low in C-14 and likely reflected C from the < 2 mm parent shale material in the soil matrix. After first removing particulate C using density or size separation, thermal fractionation can provide a rapid technique to study the age structure of MOM and how it is influenced by different OM-mineral interactions