A simple, inexpensive method for measurement of respiration (CO, evolution) under a continuous air-flow was calibrated against an i.r. gas analyzer. Regression equations were developed to apply the method to general soil respiration measurement in the laboratory. The substrate-induced respiration technique was modified. By using 120% PWHC as a standard soil water condition during incubation, in...

A new system for soil respiration measurement [P. Rochette, L.B. Flanagan, E.G. Gregorich. Separating soil respiration into plant and soil components using analyses of the natural abundance of carbon-13. Soil Sci. Soc. Am. J., 63, 1207-1213 (1999).] was modified in order to collect soil-derived CO2 for stable isotope analysis. The aim of this study was to assess the suitability of this modified...

Precipitation and temperature are important drivers of soil respiration. The role of moisture and temperature are generally explored at seasonal or inter-annual timescales; however, significant variability also occurs on hourly to daily time-scales. We used small (1.54 m(2)), throughfall exclusion shelters to evaluate the role soil moisture and temperature as temporal controls on soil CO2 efflu...

Results of a 12-yr study in an oligotrophic South Carolina salt marsh demonstrate that soil respiration increased by 795 g C m22 yr21 and that carbon inventories decreased in sediments fertilized with nitrogen and phosphorus. Fertilized plots became net sources of carbon to the atmosphere, and sediment respiration continues in these plots at an accelerated pace. After 12 yr of treatment, soil m...

We examined fine-root (< 2.0 mm diameter) respiration throughout one growing season in four northern hardwood stands dominated by sugar maple (Acer saccharum Marsh.), located along soil temperature and nitrogen (N) availability gradients. In each stand, we fertilized three 50 x 50 m plots with 30 kg NO(3) (-)-N ha(-1) year(-1) and an additional three plots received no N and served as controls. ...

It is widely known that the carbon availability in the rhizosphere is much higher than in the bulk soil. However, studies have failed to show whether microbial respiration in the rhizosphere is carbon-limited. Precise and timely measurements are lacking. We measured carbon availability index (basal respiration divided by substrate-induced respiration), and water soluble carbon in soils sampled ...

Soil respiration (Rs) is a major pathway by which fixed carbon in the biosphere is returned to the atmosphere, yet there are limits to our ability to predict respiration rates using environmental drivers at the global scale. While temperature, moisture, carbon supply, and other site characteristics are known to regulate soil respiration rates at plot scales within certain biomes, quantitative f...

Bradford et al. (2008) conclude that thermal adaptation will reduce the response of soil microbial respiration to rising global temperatures. However, we question both the methods used to calculate mass-specific respiration rates and the interpretation of the results. No clear evidence of thermal adaptation reducing soil microbial activity was produced.

The carbon isotopic composition (delta(13)C) of recently assimilated plant carbon is known to depend on water-stress, caused either by low soil moisture or by low atmospheric humidity. Air humidity has also been shown to correlate with the delta(13)C of soil respiration, which suggests indirectly that recently fixed photosynthates comprise a substantial component of substrates consumed by soil ...

The stable carbon (δC) and oxygen (δO) isotopic composition of terrestrial carbonate has been used to reconstruct late Quaternary paleoecological and paleoclimatic conditions, respectively, for many different regions of the world. Quantitative reconstructions of past variability in climate and the distribution of C3/CAM/C4 vegetation from carbonate in soils and speleothems depend upon a rigorou...