Organic C and N stabilization in a forest soil: Evidence from sequential density fractionation

In mineral soil, organic matter (OM) accumulates mainly on and around surfaces of silt- and clay-size particles. When fractionated according to particle density, C and N concentration (per g fraction) and C/N of these soil organo-mineral particles decrease with increasing particle density across soils of widely divergent texture, mineralogy, location, and management. The variation in particle density is explained potentially by two factors: (1) a decrease in the mass ratio of organic to mineral phase of these particles, and (2) variations in density of the mineral phase. The first explanation implies that the thickness of the organic accumulations decreases with increasing particle density. The decrease in C/N can be explained at least partially by especially stable sorption of nitrogenous N-containing compounds (amine, amide, and pyrrole) directly to mineral surfaces, a phenomenon well documented both empirically and theoretically. These peptidic compounds, along with ligand-exchanged carboxylic compounds, could then form a stable inner organic layer onto which other organics could sorb more readily than onto the unconditioned mineral surfaces (“onion” layering model).To explore mechanisms underlying this trend in C concentration and C/N with particle density, we sequentially density fractionated an Oregon andic soil at 1.65, 1.85, 2.00, 2.28, and 2.55 g cm⁻³ and analyzed the six fractions for measures of organic matter and mineral phase properties.All measures of OM composition showed either: (1) a monotonic change with density, or (2) a monotonic change across the lightest fractions, then little change over the heaviest fractions. Total C, N, and lignin phenol concentration all decreased monotonically with increasing density, and ¹⁴C mean residence time (MRT) increased with particle density from ca. 150 years to >980 years in the four organo-mineral fractions. In contrast, C/N, ¹³C and ¹⁵N concentration all showed the second pattern. All these data are consistent with a general pattern of an increase in extent of microbial processing with increasing organo-mineral particle density, and also with an “onion” layering model.X-ray diffraction before and after separation of magnetic materials showed that the sequential density fractionation (SDF) isolated pools of differing mineralogy, with layer-silicate clays dominating in two of the intermediate fractions and primary minerals in the heaviest two fractions. There was no indication that these differences in mineralogy controlled the differences in density of the organo-mineral particles in this soil. Thus, our data are consistent with the hypothesis that variation in particle density reflects variation in thickness of the organic accumulations and with an “onion” layering model for organic matter accumulation on mineral surfaces. However, the mineralogy differences among fractions made it difficult to test either the layer-thickness or “onion” layering models with this soil. Although SDF isolated pools of distinct mineralogy and organic-matter composition, more work will be needed to understand mechanisms relating the two factors.     

Di-tri-octahedral smectite for the prevention of post-operative diarrhea in equids with surgical disease of the large intestine: Results of a randomized clinical trial

The aim of this study was to evaluate the effects of a commercially available di-tri-octahedral (DTO) smectite product on clinical signs and prevalence of post-operative diarrhea in horses with colic associated with disease of the large intestine. Sixty-seven horses with surgical disease of the large intestine were randomly assigned to be treated with DTO smectite (n = 37; 0.5 kg via nasogastric intubation every 24 h for 3 days post-operatively) or a placebo (n = 30). The effect of treatment on fecal scores and clinical and hematological parameters, including heart rate, mucous membrane color, temperature, total white blood cell count, total neutrophil count and total plasma protein values, were determined.Horses treated with DTO smectite had a significant reduction in the prevalence of post-operative diarrhea (10.8%), compared with controls (41.4%). A significant improvement in mucous membrane color was observed 72 h post-operatively in horses receiving treatment, compared with placebo. Administration of DTO smectite to colic patients with disease of the large intestine reduced the occurrence of diarrhea in the early post-operative period.     

Escherichia coli challenge and one type of smectite alter intestinal barrier of pigs

An experiment was conducted to determine how an E. coil challenge and dietary clays affect the intestinal barrier of pigs. Two groups of 32 pigs （initial BW： 6.9 ± 1.0 kg） were distributed in a 2 x 4 factorial arrangement of a randomized complete block design （2 challenge treatments： sham or E. coil, and 4 dietary treatments： control, 0.3% smectite A, 0.3% smectite B and 0.3% zeolite）, with 8 replicates total. Diarrhea score, growth performance, goblet cell size and number, bacterial translocation from intestinal lumen to lymph nodes, intestinal morphology, and relative amounts of sulfo and sialo mucins were measured. The E. coli challenge reduced performance, increased goblet cell size and number in the ileum, increased bacterial translocation from the intestinal lumen to the lymph nodes, and increased ileal crypt depth. One of the clays （smectite A） tended to increase goblet cell size in ileum, which may indicate enhanced protection. In conclusion, E. coli infection degrades intestinal barrier integrity but smectite A may enhance it.     

Clay mineral evolution along a soil chronosequence in an Alpine proglacial area

As a consequence of global warming, additional areas will become ice-free and subject to weathering and soil formation. The most evident soil changes in the Alps will occur in proglacial areas where young soils will continuously develop due to glacier retreat. Little is known about the initial stages of weathering and soil formation, i.e. during the first decades of soil genesis. In this study, we investigated clay minerals formation during a time span 0-150 years in the proglacial area of Morteratsch (Swiss Alps). The soils developed on granitic till and were Lithic Leptosols.Mineralogical measurements of the clay (< 2 μm) and fine silt fraction (2-32 μm) were carried out using XRD (X-ray Diffraction) and DRIFT (Diffuse Reflectance Infrared Fourier Transform). Fast formation and transformation mechanisms were measured in the clay fraction. The decreasing proportion of trioctahedral phases with time confirmed active chemical weathering. Since the start of soil formation, smectite was actively formed. Some smectite (low charge) and vermiculite (high charge) was however already present in the parent material. Main source of smectite formation was biotite, hornblende and probably plagioclase. Furthermore, irregularly and regularly interstratified clay minerals (mica-HIV or mica-vermiculite) were formed immediately after the start of moraine exposure to weathering. In addition, hydroxy-interlayered smectite (HIS) as a transitory weathering product from mica to smectite was detected. Furthermore, since the start of soil evolution, kaolinite was progressively formed. In the silt fraction, only little changes could be detected; i.e. some formation of an interstratified mica-HIV or mica-vermiculite phase.The detected clay mineral formation and transformation mechanisms within this short time span confirmed the high reactivity of freshly exposed sediments, even in a cryic environment.     

典型砂姜黑土黑色物质提取方法及成分研究

土壤颜色是反映土壤发生、分类及肥力特征的一项重要物理指标。黑色土壤一般有较高的有机质含量,但砂姜黑土是低有机质含量的黑色土壤典型代表。以黄淮海平原3种典型砂姜黑土为研究对象,分别采用添加六偏磷酸钠分散剂后振荡并结合多层次超声处理(HP)、添加碳酸钠分散剂后振荡并结合多层次超声处理(SC)和仅超声波处理(US)等3种方法分散土壤,然后依次提取土壤浅色组分(颗粒态有机质(POM)、白(W)、浅白(LW))和黑色组分(浅黑(LB)、黑(B)、深黑(DB)),旨在建立土壤黑色物质的有效提取方法。结果表明,HP方法提取黑色物质(LB、B和DB)的量最多,且提取量与土壤黑度间相关性最显著(P<0.01),是提取砂姜黑土黑色物质的最佳方法。不同提取组分中的土壤黑度与有机质含量无明显相关性,砂姜黑土的显色主要取决于由蒙皂石吸附有机质形成的黑色纳米有机-无机复合体,受有机质含量的直接影响相对较小。本研究提出了一种砂姜黑土黑色物质提取方法,并初步明确了黑色物质组成特征,可为揭示砂姜黑土有机质形成与累积机制提供参考。     

Adsorption of chromium(VI) ions on Brazilian smectite: Effect of contact time,pH, concentration,and calorimetric investigation

The original smectite clay mineral has been collected from Amazon region, Brazil. The compound 2-aminomethylpyridine (AMP) was anchored onto Amazon smectite surface by heterogeneous route. The natural (SMC) and modified (SMC_AMP) smectite samples were characterized by elemental analysis, scanning electron microscopy, N₂ adsorption, X-ray diffraction, and silicon-29 and carbon-13 nuclear magnetic resonance. Due to the increment of basic centers attached to the pendant chains, the metal adsorption capability of the final chelating material, was found to be higher than the precursor. The ability of these materials to remove Cr(VI) from aqueous solution was followed by a series of adsorption isotherms at room temperature and pH 4.0. The maximum number of moles adsorbed was determined to be 1.16 and 1.87 mmol g^− 1 for SMC and SMC_AMP, respectively. In order to evaluate the clay samples as adsorbents in dynamic system, a glass column was fulfilled with clay samples (1.0 g) and it was fed with 2.0 × 10^− 4 mol dm^− 3 Cr(VI) at pH 4.0. The energetic effects caused by metal cation adsorption were determined through calorimetric titrations. Thermodynamics indicated the existence of favorable conditions for such Cr(VI)–nitrogen interactions.     

Smectite formation produced by weathering in a coarse granite saprolite in Galicia (NW Spain)

Weathering of a calcalkaline granite was studied in the south of Galicia (NW Spain) where the average annual precipitation is 1400 mm and the average annual temperature is 12°C. The original rock contains perthitic K-feldspars, plagioclases with inclusions of muscovite and opaque minerals, quartz and chloritized biotite, with apatite, zircon, sphene and opaques as accessories. In the saprolite the structure of the rock is preserved, the plagioclases show up to grade 4 weathering and the biotites, between 2 and 3. Weathering in quartz and potassium feldspar crystals is manifested only by fracturing. Biotite changes following the parallel linear model and its weathering products are interstratified biotite–vermiculite and iron oxyhydroxides. The plagioclases change to a microgranular material by pseudomorphic transformation. This material, which substitutes the plagioclase, includes small clearly delimited units which retain zones with the optic characteristics of muscovite. X-ray diffraction analyses of microsamples show that they are formed by 1:1 diocthaedral phyllosilicate, smectite and a small quantity of mica. From these facts we concluded that smectite is formed inside the plagioclase crystals, and probably originates from the inclusions of muscovite contained in these crystals, as it is suggested by the microscopic study which shows the increase in volume which occurs when the crystals of muscovite are transformed.     

Effect of north and south exposure on weathering rates and clay mineral formation in Alpine soils

A comparison was made between two soil climosequences on north- and south-facing slopes in northern Italy to determine the influence of slope aspect on soil processes. The climosequences span an elevational gradient ranging from moderate (1200 m a.s.l.) to high alpine (2420 m a.s.l.) climate zones on surfaces having an age of about 15 000 years. The soils were investigated with respect to organic C, oxalate and dithionite extractable Fe, Al and Si, elemental losses (Ca, Mg, K, Na, Fe, Al, Si, Mn) and clay minerals. The stocks of soil org. C as well as of oxalate-extractable Fe and Al was greatest in the subalpine zone near the timberline. There are no clear differences in organic C content between the soils on north- and south-facing sites. Fe-oxalate and to a lesser extent Al_o-stocks were, however, greater on north-facing sites, indicating that weathering is greater there. Eluviation and illuviation of Al and Fe within the soil profile, typical for podzolisation, was more distinctly expressed on the N slopes. The probability of ITM (Imogolite-type-material) formation in the soil seemed to be greater on south-facing sites. On the north-facing sites, element leaching was most intense in the subalpine zone close to the timberline while on the south-facing sites this was only the case for the base cations. The N slopes exhibited higher leaching of elements which generally indicates a higher weathering intensity. On south-facing sites, typical podzolisation processes were measurable only above 2000 m a.s.l. The development of smectites is also a reflection of the weathering intensity; smectite was discernible in the surface horizon at all sites on N slopes but the highest amount was detected in the sub-alpine climate zone. For the south-facing sites only in the alpine climate zone could smectite be detected. Higher temperatures and an increased number of freeze-thaw cycles on south-facing slopes should theoretically enhance rates of chemical weathering. This could, however, not be confirmed with our measurements. The degree of chemical weathering increases from the south- to the north-facing sites that are characterised by lower temperatures, lower evapotranspiration and consequently by a higher humidity. Although precipitation in Alpine regions is abundant, the availability and flux of water through the soil is the prime factor in weathering intensity.