Measuring tree root respiration using (13)C natural abundance: rooting medium matters

Tree root respiration utilizes a major portion of the primary production in forests and is an important process in the global carbon cycle. Because of the lack of ecologically relevant methods, tree root respiration in situ is much less studied compared with above-ground processes such as photosynthesis and leaf respiration. This study introduces a new (13)C natural tracer method for measuring tree root respiration in situ. The method partitions tree root respiration from soil respiration in buried root chambers. Rooting media substantially influenced root respiration rates. Measured in three media, the fine root respiration rates of longleaf pine were 0.78, 0.27 and 0.18 mg CO(2) carbon mg(-1) root nitrogen d(-1) at 25 degrees C in the native soil, tallgrass prairie soil, and sand-vermiculite mixture, respectively. Compared with the root excision method, the root respiration rate of longleaf pine measured by the field chamber method was 18% higher when using the native soil as rooting medium, was similar in the prairie soil, but was 42% lower if in the sand-vermiculite medium. This natural tracer method allows the use of an appropriate rooting medium and is capable of measuring root respiration nondestructively in natural forest conditions.     

Rhizosphere respiration varies with plant species and phenology: A greenhouse pot experiment

Assessment of particulate (>53-m) and mineral-associated (<53-m) soil organic matter (SOM) fractions is a useful approach to understand the dynamic of organic matter in soils. This study aimed to compare the long-term (9-yr) effects of no-tillage (NT) and conventional tillage (CT) on C and N stocks in the two above mentioned organic fractions in a Brazilian Acrisol. The degree of SOM humification, which has been associated with the concentration of semiquinone-type free radicals (`spin') determined by electron spin resonance (ESR), was also evaluated. Soil under no-tillage had 7.55 Mg ha<sup>–1</sup> (25%) more C and 741 kg ha<sup>–1</sup> (29%) more N than conventionally tilled soil in the 0–175-mm depth. Both particulate and mineral-associated SOM increased in the no-tilled soil. The increase of C and N stocks in the mineral-associated SOM accounted for 75% and 91% of the difference in total soil C and N stocks between NT and CT, respectively. Averaged across tillage systems, C and N stocks were respectively 4.6 and 16.8 times higher in the mineral-associated SOM than in particulate SOM. The higher C and N stocks were associated with greater recalcitrance of mineral-associated SOM to biological decomposition, resulting, probably, from its interaction with variable charge minerals. This is corroborated by a positive relationship between concentrations of C and iron oxides and kaolinite in the 53–20, 20–2 and <2-m particle size classes, of the 0–25-mm soil layer. The degree of SOM humification, assessed by ESR, decreased in both the 53–20 and 20–2-m fractions under NT. However, it was unaffected by tillage in the <2-m fraction, which normally presented the lowest `spin' concentration. Since quality as well as quantity of SOM improved in the no-tillage soil, adoption of this system is highly recommended for amelioration of degraded tropical and subtropical soils.     

Nutrient fluxes in a snow-dominated, semi-arid forest: Spatial and temporal patterns

We tested five hypotheses regarding the potential effects of precipitation change on spatial and temporal patterns of water flux, ion flux, and ion concentration in a semiarid, snowmelt-dominated forest in Little Valley, Nevada. Variations in data collected from 1995 to 1999 were used to examine the potential effects of snowpack amount and duration on ion concentrations and fluxes. Soil solution NO₃ ^–, NH₄ ⁺, and ortho-phosphate concentrations and fluxes were uniformly low, and the variations in concentration bore no relationship to snowmelt water flux inputs of these ions. Weathering and cation exchange largely controlled the concentrations and fluxes of base cations from soils in these systems; however, soil solution base cation concentrations were affected by cation concentrations during snowmelt episodes. Soil solution Cl^– and SO₄ ^2– concentrations closely followed the patterns in snowmelt water, suggesting minimal buffering of either ion by soils. In contrast to other studies, the highest concentration and the majority of ion flux from the snowpack in Little Valley occurred in the later phases of snowmelt. Possible reasons for this include sublimation of the snowpack and dry deposition of organic matter during the later stages of snowmelt. Our comparison of interannual and spatial patterns revealed that variation in ion concentration rather than water flux is the most important driver of variation in ion flux. Thus, it is not safe to assume that changes in total precipitation amount will cause concomitant changes in ion inputs to this system.