PubMed · 12775026
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Jerald L Schnoor. 2003-05-01. Internalizing the externalities.. https://doi.org/10.1021/es0324306
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The enthalpy of solution (Delta(solv)H(m)) and solubility of 1,4-naphthoquinone in CO(2) + n-pentane were measured at 308.15 K in the critical region of the binary fluid. In order to study the effect of phase behavior of the mixed solvent on Delta(solv)H(m), the experiments were carried out in the supercritical (SC) and subcritical region of the binary solvent. The density of the mixed solvent in different conditions was determined. The isothermal compressibility (K(T)) of the mixed solvent, and the partial molar volume (V(n-pentane)) of n-pentane in the solution were calculated. It was demonstrated that the Delta(solv)H(m) was negative in all conditions. Delta(solv)H(m) is nearly independent of pressure or density in all the solvents in a high-density region, in which compressibility of the solvent is very small; this indicates that the intermolecular interaction between the solvent and the solute is similar to that for liquid solutions. It is very interesting that Delta(solv)H(m) in the mixed SC fluid differs from the Delta(solv)H(m) in mixed subcritical fluids. The absolute value of Delta(solv)H(m) in the mixed SC fluid is close to that in pure SC CO(2) in the high-density region, and is much lower than that in pure SC CO(2) in the low-density region. In the mixed subcritical fluids, the Delta(solv)H(m) is also close to that in the pure CO(2) in the high-density region. However, at the same density, the absolute value of Delta(solv)H(m) in the binary subcritical fluid is larger than that in pure CO(2) in the high-compressible region of the mixed solvent. The main reason for this is that the degree of clustering in the SC solutions is small at the density in which the degree of clustering is large in the subcritical solutions. It can be concluded that solubility enhancement by n-pentane in the mixed SC fluid is entropy driven. In contrast, the solubility enhancement by n-pentane in subcritical fluids is enthalpy driven. The intermolecular interaction in the SC solutions and subcritical solutions can be significantly different even if their densities are the same.
Despite the great interest concerning the relationship between species diversity and ecosystem functioning, there is virtually no knowledge as to how the diversity of decomposer microbes influences the decomposition rate of soil organic matter. We established a microcosm study in which the number of soil fungi was investigated in relation to the system's ability to (i) degrade raw coniferous forest humus, and (ii) use resources that were either added to the systems or released into the soils after a disturbance (drought). With the exception of the most diverse treatment, in each of the six replicates of each of the six diversity treatments (1, 3, 6, 12, 24 or 43 taxa), fungal taxa were randomly chosen from a pool of 43 commonly isolated fungal species of raw humus. Two months after initiation of the study CO2 production increased as fungal diversity increased, but in the species-poor end of the diversity gradient only. Addition of various energy resources to the microcosms generally increased the level of soil respiration but did not affect the shape of the diversity-CO2-production curve. Rewetting the soil after severe drought resulted in a rapid flush of CO2, particularly in the most diverse communities. The biomass of the fungi in the non-disturbed soils, and soil NH4-N concentration and soil pH in both disturbed and non-disturbed systems were slightly but significantly higher in the diverse than in the simple systems. Fungal species richness had no influence on the organic matter content of the humus at the end of the experiment. The results suggest that the functional efficiency of fungal communities can increase with the number of fungal taxa. This diversity effect was, however, significant at the species-poor end of the diversity gradient only, which implies considerable functional equivalency (redundancy) among the decomposer fungi.
It has generally been assumed that the photosynthetic quantum yield of all C3 plants is essentially the same for all unstressed leaves at the same temperature and CO2 and O2 concentrations. However, some recent work by H.C. Timm et al. (2002, Trees 16:47-62) has shown that quantum yield can be reduced for some time after leaves have been exposed to darkness. To investigate under what light conditions quantum yield can be reduced, we carried out a number of experiments on leaves of a partial-shade (unlit greenhouse)-grown Coleus blumei Benth. hybrid. We found that after leaves had been exposed to complete darkness, quantum yield was reduced by about 60%. Only very low light levels were needed for quantum yield to be fully restored, with 5 micromol quanta m(-2) s(-1) being sufficient for 85% of the quantum yield of fully induced leaves to be achieved. Leaves regained higher quantum yields upon exposure to higher light levels with an estimated time constant of 130 s. It was concluded that the loss of quantum yield would be quantitatively important only for leaves growing in very dense understoreys where maximum light levels might not exceed 5 micromol quanta m(-2) s(-1) even in the middle of the day. Most leaves, even in understorey conditions, do, however, experience light levels in excess of 5 micromol quanta m(-2) s(-1) over periods where they obtain most of their carbon so that the loss of quantum yield would affect total carbon gain of those leaves only marginally.