We combined year-round eddy covariance with biometry and biomass harvests along a chronosequence of boreal forest stands that were 1, 6, 15, 23, 40, $ 74, and $ 154 years old to understand how ecosystem production and carbon stocks change during recovery from stand-replacing crown fire. Live biomass (C live ) was low in the 1-and 6-year-old stands, and increased following a logistic pattern to high levels in the 74-and 154-year-old stands. Carbon stocks in the forest floor (C forest floor ) and coarse woody debris (C CWD ) were comparatively high in the 1-year-old stand, reduced in the 6-through 40-year-old stands, and highest in the 74-and 154-year-old stands. Total net primary production (TNPP) was reduced in the 1-and 6-year-old stands, highest in the 23-through 74-year-old stands and somewhat reduced in the 154-year-old stand. The NPP decline at the 154-year-old stand was related to increased autotrophic respiration rather than decreased gross primary production (GPP). Net ecosystem production (NEP), calculated by integrated eddy covariance, indicated the 1-and 6-year-old stands were losing carbon, the 15-year-old stand was gaining a small amount of carbon, the 23-and 74-year-old stands were gaining considerable carbon, and the 40-and 154-year-old stands were gaining modest amounts of carbon. The recovery from fire was rapid; a linear fit through the NEP observations at the 6-and 15-year-old stands indicated the transition from carbon source to sink occurred within 11-12 years. The NEP decline at the 154-year-old stand appears related to increased losses from C live by tree mortality and possibly from C forest floor by decomposition. Our findings support the idea that NPP, carbon production efficiency (NPP/GPP), NEP, and carbon storage efficiency (NEP/TNPP) all decrease in old boreal stands.
We combined observations from four eddy covariance towers with remote sensing to better understand the altitudinal patterns of climate, plant phenology, Gross Ecosystem CO2Uptake, and Evapotranspiration (ET) around the Upper Kings River basin in the southern Sierra Nevada Mountains. Precipitation (P) increased with elevation to ∼500 m, and more gradually at higher elevations, while vegetation graded from savanna at 405 m to evergreen oak and pine forest to mid‐montane forest to subalpine forest at 2700 m. CO2uptake and transpiration at 405 m peaked in spring (March to May) and declined in summer; gas exchange at 1160 and 2015 m continued year‐round; gas exchange at 2700 m peaked in summer and ceased in winter. A phenological threshold occurred between 2015 and 2700 m, associated with the development of winter dormancy. Annual ET and Gross Primary Production were greatest at 1160 and 2015 m and reduced at 405 m coincident with less P, and at 2700 m coincident with colder temperatures. The large decline in ET above 2015 m raises the possibility that an upslope redistribution of vegetation with climate change could cause a large increase in upper elevation ET. We extrapolated ET to the entire basin using remote sensing. The 2003–11 P for the entire Upper Kings River basin was 984 mm y−1 and the ET was 429 mm y−1, yielding a P‐ET of 554 mm y−1, which agrees well with the observed Kings River flow of 563 mm y−1. ET averaged across the entire basin was nearly constant from year to year.
Decomposition of O horizon organic matter made up 20% or less of soil respiration in the younger (o40 years since fire) stands, increasing to $ 50% in mature stands. This is a minimum for total heterotrophic contribution, since mineral soil CO 2 had D 14 C close to or less than those we have assigned to autotrophic respiration. Decomposition of old organic matter in mineral soils clearly contributed to soil respiration in younger stands in 2003, a very dry year, when D 14C of soil respiration in younger successional stands dropped below those of the atmospheric CO 2 .
a b s t r a c tThe relative importance of dispersal limitation versus environmental filtering for community assembly has received much attention for macroorganisms. These processes have only recently been examined in microbial communities. Instead, microbial dispersal has mostly been measured as community composition change over space (i.e., distance decay).Here we directly examined fungal composition in airborne wind currents and soil fungal communities across a 40 000 km 2 regional landscape to determine if dispersal limitation or abiotic factors were structuring soil fungal communities. Over this landscape, neither airborne nor soil fungal communities exhibited compositional differences due to geographic distance. Airborne fungal communities shifted temporally while soil fungal communities were correlated with abiotic parameters. These patterns suggest that environmental filtering may have the largest influence on fungal regional community assembly in soils, especially for aerially dispersed fungal taxa. Furthermore, we found evidence that dispersal of fungal spores differs between fungal taxa and can be both a stochastic and deterministic process. The spatial range of soil fungal taxa was correlated with their average regional abundance across all sites, which may imply stochastic dispersal mechanisms. Nevertheless, spore volume was also negatively correlated with spatial range for some species. Smaller volume spores may be adapted to long-range dispersal, or establishment, suggesting that deterministic fungal traits may also influence fungal distributions. Fungal life-history traits may influence their distributions as well. Hypogeous fungal taxa exhibited high local abundance, but small spatial ranges, while epigeous fungal taxa had lower local abundance, but larger spatial ranges. This study is the first, to our knowledge, to directly sample air dispersal and soil fungal communities simultaneously across a regional landscape. We provide some of the first evidence that soil fungal communities are mostly assembled through environmental filtering and experience little dispersal limitation.
Abstract. We measured soil respiration during two winters in three different ecotypes of the BOREAS northern study area. The production of CO2 was continuous throughout the winter and, when totaled for the winter of 1994-1995, was equivalent to the release of --•40-55 g C/m 2 from the soil surface. As soils cooled in the early winter, the CO2 production rate decreased in a manner that appeared to be exponentially related to shallow soil temperatures. This exponential relationship was not observed when soils began to warm, possibly indicating that there may be additional or different processes responsible for increased CO2 production during winter warming events. We also measured CO2 concentrations in soil gas and the A•4C of the soil CO2. These measurements show that the CO2 produced in winter is not simply the return to the atmosphere of the carbon fixed during the previous growing season. We suggest that the wintertime production of CO2 originates, at least in part, from the decomposition of old organic carbon stored at depth in the soil.
We deployed a mesonet of year-round eddy covariance towers in boreal forest stands that last burned in $1850, $1930, 1964, 1981, 1989, 1998, and 2003 to understand how CO 2 exchange and evapotranspiration change during secondary succession. We used MODIS imagery to establish that the tower sites were representative of the patterns of secondary succession in the region, and Landsat images to show that the individual stands have changed over the last 22 years in ways that match the spatially derived trends. The eddy covariance towers were well matched, with similar equipment and programs, which maximized site-to-site precision and allowed us to operate the network in an efficient manner. The six oldest sites were fully operational for $90% of the growing season and $70% of the dormant season from 2001 or 2002 to 2004, with most of the missing data caused by low battery charge or bad signals from the sonic anemometers. The rates of midday growing-season CO 2 uptake recovered to preburn levels within 4 years of fire. The seasonality of land-atmosphere exchange and growing-season length changed markedly with stand age. The foliage in the younger stands (1989, 1998, and 2003 burns) was almost entirely deciduous, which resulted in comparatively short growing seasons that lasted $65 days. In contrast, the older stands (1850, 1930, 1964, and 1981) were mostly evergreen, which resulted in comparatively long growing seasons that lasted $130 days. The eddy covariance mesonet approach we describe could be used within the context of other ecological experimental designs such as controlled manipulations and gradient comparisons.
[1] A mechanistic understanding of soil respiration is a major impediment to predicting terrestrial C fluxes spatially and temporally. Automated measurements of soil respiration offer the high-resolution information necessary to observe temporal variation in soil respiration, but spatially these measurements are under-represented in water-limited and non-forested ecosystems. We measured soil respiration with automated chambers over the growing season, at two sites with the same semi-arid climate, but with different dominant vegetation, perennial grasses and shrubs in the Owens Valley, CA, USA. An isotope mass balance technique was used to partition soil respiration into autotrophic and heterotrophic components at two time points, early and late growing season. Results showed large differences in the magnitude of growing season soil respiration between the two sites (910 versus 126 g C m À2 for grasses and shrubs respectively over 5 months). We attribute this to site differences in soil water availability and belowground allocation and productivity. Diel patterns of soil respiration between the two sites were similar. Temperature explained most of the diel variability in the early growing season, when soil moisture was greatest. As soil moisture declined over the growing season, diel patterns became increasingly decoupled temporally from temperature due to increased water-limitation on surface heterotrophic sources and hypothesized strong photosynthetic control over soil respiration rates. Partitioning of soil respiration into autotrophic and heterotrophic sources showed the dominance of autotrophic sources across seasons and ecosystems. However, heterotrophic respiration was more dynamic from early to late growing season, declining in the grass ecosystem; and a surprising increase in the shrub ecosystem, attributed to warming of the soil profile enhancing microbial decomposition at depth.Citation: Carbone, M. S., G. C. Winston, and S. E. Trumbore (2008), Soil respiration in perennial grass and shrub ecosystems: Linking environmental controls with plant and microbial sources on seasonal and diel timescales,
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