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  • 1
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Drought control over conductance and assimilation was assessed using eddy flux and meteorological data monitored during four summer periods from 1998 to 2001 above a closed canopy of the Mediterranean evergreen oak tree Quercus ilex. Additional discrete measurements of soil water content and predawn leaf water potential were used to characterize the severity of the drought.Canopy conductance was estimated through the big-leaf approach of Penman–Monteith by inverting latent heat fluxes. The gross primary production (GPP) was estimated by adding ecosystem respiration to net ecosystem exchange. Ecosystem respiration was deduced from night flux when friction velocity (u*) was greater than 0.35 m s−1. Empirical equations were identified that related maximal canopy conductance and daily ecosystem GPP to relative soil water content (RWC), the ratio of current soil water content to the field capacity, and to the predawn leaf water potential. Both variables showed a strong decline with soil RWC for values lower than 0.7. The sharpest decline was observed for GPP. The curves reached zero for RWC=0.41 and 0.45 for conductance and GPP, respectively. When the predawn leaf water potential was used as a surrogate for soil water potential, both variables showed a hyperbolic decline with decreasing water potential.These results were compared with already published literature values obtained at leaf level from the same tree species. Scaling up from the leaf to ecosystem highlighted the limitation of two big-leaf representations: Penman–Monteith and Sellers' Π factor. Neither held completely for comparing leaf and canopy fluxes. Tower measurements integrate fluxes from foliage elements clumped at several levels of organization: branch, tree, and ecosystem. The Q. ilex canopy exhibited non-random distribution of foliage, emphasizing the need to take into account a clumping index, the factor necessary to apply the Lambert–Beer law to natural forests.Our results showed that drought is an important determinant in water losses and CO2 fluxes in water-limited ecosystems. In spite of the limitations inherent to the big-leaf representation of the canopy, the equations are useful for predicting the influence of environmental factors in Mediterranean woodlands and for interpreting ecosystem exchange measurements.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: This paper discusses the advantages and disadvantages of the different methods that separate net ecosystem exchange (NEE) into its major components, gross ecosystem carbon uptake (GEP) and ecosystem respiration (Reco). In particular, we analyse the effect of the extrapolation of night-time values of ecosystem respiration into the daytime; this is usually done with a temperature response function that is derived from long-term data sets. For this analysis, we used 16 one-year-long data sets of carbon dioxide exchange measurements from European and US-American eddy covariance networks. These sites span from the boreal to Mediterranean climates, and include deciduous and evergreen forest, scrubland and crop ecosystems.We show that the temperature sensitivity of Reco, derived from long-term (annual) data sets, does not reflect the short-term temperature sensitivity that is effective when extrapolating from night- to daytime. Specifically, in summer active ecosystems the long-term temperature sensitivity exceeds the short-term sensitivity. Thus, in those ecosystems, the application of a long-term temperature sensitivity to the extrapolation of respiration from night to day leads to a systematic overestimation of ecosystem respiration from half-hourly to annual time-scales, which can reach 〉25% for an annual budget and which consequently affects estimates of GEP. Conversely, in summer passive (Mediterranean) ecosystems, the long-term temperature sensitivity is lower than the short-term temperature sensitivity resulting in underestimation of annual sums of respiration.We introduce a new generic algorithm that derives a short-term temperature sensitivity of Reco from eddy covariance data that applies this to the extrapolation from night- to daytime, and that further performs a filling of data gaps that exploits both, the covariance between fluxes and meteorological drivers and the temporal structure of the fluxes. While this algorithm should give less biased estimates of GEP and Reco, we discuss the remaining biases and recommend that eddy covariance measurements are still backed by ancillary flux measurements that can reduce the uncertainties inherent in the eddy covariance data.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Several studies have shown multiple confounding factors influencing soil respiration in the field, which often hampers a correct separation and interpretation of the different environmental effects on respiration. Here, we present a controlled laboratory experiment on undisturbed organic and mineral soil cores separating the effects of temperature, drying–rewetting and decomposition dynamics on soil respiration. Specifically, we address the following questions:〈list xml:id="l1" style="custom"〉1Is the temperature sensitivity of soil respiration (Q10) dependent on soil moisture or soil organic matter age (incubation time) and does it differ for organic and mineral soil as suggested by recent field studies.2How much do organic and mineral soil layers contribute to total soil respiration?3Is there potential to improve soil flux models of soil introducing a multilayer source model for soil respiration?Eight organic soil and eight mineral soil cores were taken from a Norway spruce (Picea abies) stand in southern Germany, and incubated for 90 days in a climate chamber with a diurnal temperature regime between 7 and 23°C. Half of the samples were rewetted daily, while the other half were left to dry and rewetted thereafter. Soil respiration was measured with a continuously operating open dynamic soil respiration chamber system. The Q10 was stable at around 2.7, independent of soil horizon and incubation time, decreasing only slightly when the soil dried. We suggest that recent findings of the Q10 dependency on several factors are emergent properties at the ecosystem level, that should be analysed further e.g. with regard to rhizosphere effects. Most of the soil CO2 efflux was released from the organic samples. Initially, it averaged 4.0 μmol m−2 s−1 and declined to 1.8 μmol m−2 s−1 at the end of the experiment. In terms of the third question, we show that models using only one temperature as predictor of soil respiration fail to explain more than 80% of the diurnal variability, are biased with a hysteresis effect, and slightly underestimate the temperature sensitivity of respiration. In contrast, consistently more than 95% of the diurnal variability is explained by a dual-source model, with one CO2 source related to the surface temperature and another CO2 source related to the central temperature, highlighting the role of soil surface processes for ecosystem carbon balances.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1365-2486
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Geography
    Notes: Eddy covariance and sapflow data from three Mediterranean ecosystems were analysed via top-down approaches in conjunction with a mechanistic ecosystem gas-exchange model to test current assumptions about drought effects on ecosystem respiration and canopy CO2/H2O exchange. The three sites include two nearly monospecific Quercus ilex L. forests – one on karstic limestone (Puéchabon), the other on fluvial sand with access to ground water (Castelporziano) – and a typical mixed macchia on limestone (Arca di Noè). Estimates of ecosystem respiration were derived from light response curves of net ecosystem CO2 exchange. Subsequently, values of ecosystem gross carbon uptake were computed from eddy covariance CO2 fluxes and estimates of ecosystem respiration as a function of soil temperature and moisture. Bulk canopy conductance was calculated by inversion of the Penman-Monteith equation. In a top-down analysis, it was shown that all three sites exhibit similar behaviour in terms of their overall response to drought. In contrast to common assumptions, at all sites ecosystem respiration revealed a decreasing temperature sensitivity (Q10) in response to drought. Soil temperature and soil water content explained 70–80% of the seasonal variability of ecosystem respiration. During the drought, light-saturated ecosystem gross carbon uptake and day-time averaged canopy conductance declined by up to 90%. These changes were closely related to soil water content. Ecosystem water-use efficiency of gross carbon uptake decreased during the drought, regardless whether evapotranspiration from eddy covariance or transpiration from sapflow had been used for the calculation. We evidence that this clearly contrasts current models of canopy function which predict increasing ecosystem water-use efficiency (WUE) during the drought. Four potential explanations to those results were identified (patchy stomatal closure, changes in physiological capacities of photosynthesis, decreases in mesophyll conductance for CO2, and photoinhibition), which will be tested in a forthcoming paper. It is suggested to incorporate the new findings into current biogeochemical models after further testing as this will improve estimates of climate change effects on (semi)arid ecosystems' carbon balances.
    Type of Medium: Electronic Resource
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