The distribution of nitrogen in some highly organic tropical volcanic soils

The qualitative and quantitative distribution of N-compounds in 10 tropical soils, and in a number of humic materials extracted from representative samples thereof, was determined after 6 N HCl hydrolysis.Eighty to 98% of the total N in the soils and humic materials was hydrolysable by 6n HCl. Slightly less than one half the hydrolysable N in the soils and humic fractions consisted of amino acids. Well-drained soils and fulvic acids extracted from them contained unusually high concentrations of the acidic amino acids, aspartic and glutamic acids. Between 80 and 95% of the amino acids in the soils was accounted for in the humic materials + NaOH-insoluble organic residues. NH⁺₄-N released by acid hydrolysis was generally higher for the soil samples than for the humic materials. Amino sugar-N constituted relatively small proportions of the total N in the soils and humic fractions.Our data suggest that large quantities of amorphous allophanic materials coupled with relatively high enzymic activity are responsible for the observed accumulation of acidic amino acids in the well-drained tropical volcanic soils.     

Volatilization of sulfur from unamended and sulfate-treated soils

Volatilization of sulfur from unamended and sulfate-treated soils was studied by sensitive gas chromatographic techniques using a flame photometric detector fitted with a sulfur filter. The soils employed were surface samples of 25 Iowa soils selected to obtain a wide range in properties. No release of volatile sulfur compounds was detected when 11 of these soils were incubated under aerobic or waterlogged conditions before or after treatment with sulfate (400 μg sulfate S/g soil). Fourteen soils released volatile sulfur compounds when incubated under waterlogged conditions before and after addition of sulfate, but only 4 of these soils released volatile sulfur compounds when incubated under aerobic conditions. Where volatilization of sulfur was observed, the volatile sulfur detected was identified as dimethyl sulfide or as dimethyl sulfide associated with smaller amounts of carbonyl sulfide, carbon disulfide, methyl mercaptan, and (or) dimethyl disulfide. No trace of hydrogen sulfide was detected. Where release of volatile sulfur was observed, the amount of sulfur volatilized at 30°C in 60 days under aerobic or waterlogged conditions was very small and did not account for more than 0–05% of the sulfur in the unamended or sulfate-treated soils studied. It is concluded that gaseous loss of sulfur from unamended or sulfate-treated soils is insignificant under conditions likely to be encountered in the field.     

The production of N-nitrosoiminodiacetate from nitrilotriacetate and nitrate by microorganisms growing in mixed culture

Mixed populations of microorganisms growing in a recycling soil percolator produced N-nitrosoiminodiacetate (NIDA) after 30 days growth using sodium nitrilotriacetate (NTA), a detergent additive, and NaNO₃ as C and N source respectively. Control experiments using autoclaved soil or substituting either acetate (C source) or NH⁺₄ (N source) did not show any N-nitroso derivative production. Five distinct strains of microorganisms were isolated which could grow on an NTA/NO^?₃ minimal medium but none produced NIDA in pure culture. Mixed cultures of two strains of Pseudomonas produced NIDA after 4 days percolation, using glass beads as a support. Cell-free extracts of the mixed cultures synthesized NIDA after 30 min incubation at 30°C with an activity of 27 μmoles NIDA produced/mg protein h^?1. Physical separation of the two organisms and the cell-free extracts by a dialysis membrane in a chamber determined that only one of the two organisms was responsible for the synthesis of NIDA, but the production was dependent upon the presence of the other organism. The possible relationship between the two organisms is discussed.     

Substances interfering with the gas-liquid chromatographic determination of T-2 mycotoxin.

Two substances interfering with the gas-liquid chromatographic (GLC) detection of T-2 mycotoxin were identified as 1-glyceryl-monooleate and 1-glycerylmonolinoleate. These monoglycerides are natural products formed by species of Fusarium growing on cereal grains and are also additives contained in liquid vegetable and animal fats added to the feed mixture. The monoglycerides can be removed from the analytical sample by resolution by thin layer chromatography prior to separation by GLC. Trimethylsilyl ether derivatives of the monoglycerides and T-2 toxin have almost identical retention times on 3% OV-1 columns, whereas the trifluoroacetyl and pentafluoropropionyl derivatives give baseline separation on the same column. The monoglycerides can be misidentified as the T-2 toxin in analyses involbing GLC.     

Mineralogisch-chemische umwandlungen bei der verwitterung pyroklastischer gesteine auf teneriffa (Kanarische Inseln)

In a weathering profile on pyroclastic material four phases of volcanic activity could be defined by mineralogical analysis. Halloysite in 10 Å- and 7 Å-modifications is the predominant new mineral formed by weathering processes. Various degrees of development of this clay-mineral were found in scanning microscopy.The paragenesis of gibbsite, ilmenite and anatase is characteristic for horizons of most intense weathering. The gibbsite found in distinct layers indicates an alteration of climatic conditions between eruption-stages 3 and 4. Absolute age determinations on potash-felspars from a layer of stage 3 yield 1.53 mio. years (+ 10%).     

Sodium bicarbonate as an extractant for soil phosphate III. Effects of the buffering capacity of a soil for phosphate

An index of the buffering capacity for phosphate of a group of soils was obtained by measuring adsorption of phosphate from dilute solutions of calcium chloride. The effect of buffering capacity on the amount of phosphate initially displaced by solutions of sodium bicarbonate and on the amount of secondary adsorption from bicarbonate was then studied. These two effects were separated using a regression procedure in which the soil: solution ratio was the independent variable.As buffering capacity increased the amount of phosphorus initially displaced decreased and the amount of secondary adsorption increased. Both these changes resulted in a decrease in the amount of phosphate in the extract. The effect of buffering capacity was greater with the Olsen method (soil : solution ratio 1 : 20; 30 min) than with the Colwell method (soil : solution ratio 1 : 100; 16 h). The relation between phosphorus extracted and buffering capacity was of a similar shape to that between effectiveness of fertilizer and buffering capacity. However, the first relation depends on the conditions of extraction and the second on the kind of plant grown and on the conditions of growth. Hence the two relations do not necessarily coincide.The effect of buffering capacity on the proportion of added phosphate initially displaced from the soil became more marked as the period of incubation prior to extraction was increased. Bicarbonate soil tests would therefore indicate that, on soils of low buffering capacity, the decrease with time in availability of applied phosphate would be smaller than on soils of high buffering capacity. This effect differs from that observed with plants.