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911.
In well-aerated culture solutions Ca-montmorillonite at 0.25% concentration markedly accelerated and increased growth, glucose consumption and CO2 evolution by various Streptomyces, Micromonospora and Nocardia species. The montmorillonite was a little more active than Ca-humate and was usually still but somewhat less effective when confined to dialysis tubing. Ca-exchange resin, Na2SiO3 and finely powdered CaCO3 exerted very little or no effect. In many cultures the relation of glucose consumption to biomass formation indicated a more efficient use of the glucose C for cell synthesis in the presence of clay. In other cultures the greater biomass formation was associated with a more rapid and complete utilization of the glucose present. 相似文献
912.
Pyrolysis mass-spectra from a sample of the A1-horizon of a soil from southern Spain showed predominant peaks related to furan derivatives similar to those observed from complex polysaccharides in which not only hexoses but also pentoses and deoxyhexoses were constituent units. Smaller peaks, typical for protein materials and phenolic units, were also observed. On the other hand, typical peaks for the methoxyphenols of lignins were very small and indicated only limited amounts of undecomposed lignin residues in this soil sample. Peaks related to benzene or toluene were also very small.Humic acid samples from this soil showed much more prominent signals related to protein materials, benzene and phenolic derivatives and weaker polysaccharide-related signals than did the entire sample. Typical lignin related peaks were small or insignificant. Spectra from the grey or brown humidic acid fractions were much like those of the parent humic acid. Brown humic acid, however, showed stronger signals for nitrogen and sulphur compounds, indicating a higher content of protein-like materials in this fraction. Preparations of humic acid hydrolyzed by 6 N HCl showed in their pyrolysis products a marked increase in phenols and methoxyphenols.In its pyrogram, humin resembled humic acid, but signals for complex polysaccharides were more evident. Lignin-like materials seem not to be higher in this fraction. Hymatomelanic acid showed prominent signals related to polysaccharides and lignin. Pyrograms from the soil polysaccharides showed the characteristic pattern of a complex polysaccharide with the presence of fragments from polymers of amino acids or amino sugars. Fulvic acid spectra showed obvious dissimilarities to those from humic acid in that signals for protein, as well as those related to phenols, were low. Depending upon the isolation method, the fulvic acid preparations showed differing signals related to polysaccharide or phenolic materials. 相似文献
913.
Six New Zealand topsoils of widely different origins and properties were subjected to 6m HC1 hydrolysis and the distribution of N fractions and amino acids were determined qualitatively and quantitatively.Of the total-N in the soils studied 83–91%, was hydrolysable with 6m HCl. The largest proportion of the hydrolysable N was α-amino acid N (38– 42%). followed by hydrolysable-unknown N (HUN) (14–24%), and NH4+-N (14–22%). A significant proportion (25–50%) of the HUN fraction was accounted for by the non α-amino acid-N. Oxidative (3% H2O2) hydrolysis released N-phenoxy amino acid-N and possibly N-compounds which were complexed with phenols and sugars. All soils had a similar amino-acid composition with a predominance of acidic amino-acids. 相似文献
914.
Freshly cleaved mica sheets with aluminium- or iron(III)-hydroxy species on the cationexchange surface were prepared by suitable treatment with AlCl3 or FeCl3. These surfaces were considered as model soilk mineral surfaces and their interaction with phosphate studied using techniques previously developed for the study of single planar surfaces.Adsorption isotherms for both the iron(III) and aluminium systems were very similar and could be interpreted as two Freundlich isotherms indicating two different adsorption processes, one operating below a solution concentration of 10?5 M and thee other above. Results obtained from the continuous monitoring of adsorption indicate that a rearrangement of adsorbed phosphate occurs with time on both the aluminium- and iron(III)hydroxy surfaces. This rearrangement reduces the rate of desorption and could be a cause of phosphate fixation in soils. 相似文献
915.
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919.
The relative persistence of 2,4-D, MCPA and 2,4,5-T in some Saskatchewan soils was assessed under laboratory conditions. Under moist conditions, 2,4-D and MCPA showed half-life times of between 14 and 41 days but the MCPA half-life was usually 1 or 2 days longer. 2,4,5-T exhibited a half-life period over twice the length of the other chemicals. The half-life times were directly correlated to microbial plate counts, the larger numbers of soil microorganisms being associated with shorter residence times. Half-lives depended on soil moisture content and the best moisture levels for chemical loss appeared to be just less than field capacity. The use of 14C in 2,4-D incubation studies showed that the initial cleavage of the 2,4-D molecule was associated with the ether linkage and was not a decarboxylation. 相似文献
920.
Macroconidia of Fusarium solani f. cucurbitae were placed into natural soil, incubated for various times, recovered and examined by light and transmission electron microscopy. Lysis of macroconidia and formation of chlamydospores were studied and the fine structure of these propagules and their associated microflora was investigated. The two most obvious features of chlamydospore morphology were the sloughing of outer wall layers and the accretion of micro-fibrillar elements adjacent to the plasmalemma. Chlamydospore formation was partially suppressed by addition of nitrogenous compounds to the soil. 相似文献