European Journal of Soil Science
Công bố khoa học tiêu biểu
* Dữ liệu chỉ mang tính chất tham khảo
Việc đưa rơm vào đất đã được khuyến khích như một giải pháp thay thế cho việc đốt rơm tại chỗ, điều này đang diễn ra ở nhiều vùng trồng lúa. Tuy nhiên, thực hành này có thể dẫn đến sự thay đổi trong tính chất keo của đất sét, điều này có thể làm tăng cường sự mất mát của đất sét và dinh dưỡng. Nghiên cứu này nhằm chứng minh ảnh hưởng của bột rơm được thiết kế với kích thước vi mô lên các tính chất keo của hai loại đất sét, đó là đất sét illite và kaolinite. Kỹ thuật tán xạ ánh sáng động đã được kết hợp với phương pháp ống nghiệm để đánh giá sự thay đổi theo thời gian về kích thước hạt, điện thế zeta và khả năng phân tán cho các huyền phù của bột rơm và các hỗn hợp của nó với đất sét illite và kaolinite. Dữ liệu từ các thí nghiệm động học trong khoảng thời gian 20 ngày cho thấy bột rơm đã làm tăng đáng kể khả năng phân tán của đất sét. Phát hiện cho thấy các hạt rơm mang điện tích âm; do đó, việc đưa bột rơm vào các huyền phù đất sét đã làm tăng số lượng điện tích âm trong hệ thống, từ đó tăng cường các lực đẩy nội bộ và cuối cùng thúc đẩy sự phân tán của đất sét. Hơn nữa, một số quá trình tương tác, đó là sự phân hủy sinh học và hòa tan của phytolith (silica trong rơm), dẫn đến việc giải phóng chất hữu cơ hòa tan và silicon, điều này làm tăng cường khả năng phân tán của đất sét. Ngoài nhận thức “truyền thống” về tác động của việc đưa rơm vào đất, chẳng hạn như tạo ra môi trường độc hại, môi trường thiếu oxy hoặc tăng lượng phát thải CH4, sự thay đổi trong các tính chất keo của đất sét cũng cần được nhấn mạnh. Chúng tôi đề xuất rằng việc đưa rơm vào đất cần có thêm các giải pháp để ngăn ngừa sự mất mát đất sét.
Bột rơm đã được kiểm tra về khả năng ảnh hưởng đến các tính chất keo của đất sét Phát hiện rằng các hạt rơm mang điện tích âm Việc đưa bột rơm vào tăng cường lực đẩy và tạo điều kiện cho sự phân tán của đất sét Vi sinh vật,
The response of soil respiration (
Mid‐infrared diffuse reflectance spectroscopy can provide rapid, cheap and relatively accurate predictions for a number of soil properties. Most studies have found that it is possible to estimate chemical properties that are related to surface and solid material composition. This paper focuses on prediction of physical and mechanical properties, with emphasis on the elucidation of possible mechanisms of prediction. Soil physical properties that are based on pore‐space relationships such as bulk density, water retention and hydraulic conductivity cannot be predicted well using MIR spectroscopy. Hydraulic conductivity was measured using a tension‐disc permeameter, excluding the macropore effect, but MIR spectroscopy did not give a good prediction. Properties based on the soil solid composition and surfaces such as clay content and shrink‐swell potential can be predicted reasonably well. Macro‐aggregate stability in water can be predicted reasonably as it has a strong correlation with carbon content in the soil. We found that most of the physical and mechanical properties can be related back to the fundamental soil properties such as clay content, carbon content, cation exchange capacity and bulk density. These connections have been explored previously in pedotransfer functions studies. The concept of a spectral soil inference system is reiterated: linking the spectra to basic soil properties and connecting basic soil properties to other functional soil properties via pedotransfer functions.
This work aimed to evaluate the potential of mid‐infrared reflectance spectroscopy (MIRS) to predict soil organic and inorganic carbon contents with a 2086‐sample set representative of French topsoils (0–30 cm). Ground air‐dried samples collected regularly using a 16 × 16‐km grid were analysed for total (dry combustion) and inorganic (calcimeter) carbon; organic carbon was calculated by difference. Calibrations of MIR spectra with partial least square regressions were developed with 10–80% of the set and five random selections of samples. Comparisons between samples with contrasting organic or inorganic carbon content and regression coefficients of calibration equations both showed that organic carbon was firstly associated with a wide spectral region around 2500–3500 cm−1 (which was a reflection of its complex nature), and inorganic carbon with narrow spectral bands, especially around 2520 cm−1. Optimal calibrations for both organic and inorganic carbon were achieved by using 20% of the total set: predictions were not improved much by including more of the set and were less stable, probably because of atypical samples. At the 20% rate, organic carbon predictions over the validation set (80% of the total) yielded mean
The packing of elementary particles in soil largely determines the properties that depend on the textural soil pore space, but is studied little. The relations between packing and size and nature of soil particles were studied using fractions of clay, silt and sand, mixed when wet and then dried. Ternary mixtures (clay:silt:sand) were compared with binary mixtures (clay:silt, clay:sand). The pore space of the mixtures was studied using mercury porosimetry and scanning electron microscopy. In all the mixtures the textural pore space was divided into two compartments: (1) lacunar pores due to the presence of skeleton particles and to the shrinkage of the clay phase between these particles, and (2) the clay–fabric pores due to the packing of the clay. In the ternary mixtures, lacunar pores could be divided into two classes: (1) those due to sand particles within the clay–slit phase considered as a single phase, and (2) those due to silt particles within this same phase. For certain mixtures, lacunar pores, referred to as hidden lacunar pores, were not interconnected but were occluded. This occurred both for hidden pores caused by the presence of sand and occluded by the clay–slit phase, and for hidden pores caused by the presence of silt and occluded by the clay phase. The relations between these types of textural pores and the proportions of different size fractions in the mixtures provide guidelines for making optimum use of the particle‐size characteristics of the soil to determine its properties.
Although the effect of experimental warming on soil microorganisms has been well documented at surface horizons, less is known about its influence in subsurface horizons. An experiment was therefore carried out in an alpine meadow on the
In the detritusphere, particulate organic matter offers new sites for microorganisms, whereas soluble substrates are transported into the adjacent soil. We investigated how mechanisms of solute transport affect microbial abundance and function in the detritusphere. In a first experiment, transport was restricted to diffusion, whereas in a second experiment it was dominated by convection. Two soil moisture contents were established in each experiment. When diffusion was the exclusive transport mechanism, the addition of maize litter induced distinct gradients in enzyme activities, soil organic C content and microbial biomass to a depth of 1.5–2.8 mm. Convection enlarged these gradients to 2.5–3.0 mm. The moisture regime modified the temporal pattern of diffusive C transport, microbial growth and enzyme release by inducing faster transport at large water contents. Convective transport seemed to be unaffected by soil moisture content. Using a convective‐diffusive transport model with first‐order decay, it was possible to simulate the observed activity profiles. The results indicate that the spatial dimension of the detritusphere is governed by the ratio between decay rate of available substrates and transport rate. Bacteria and fungi showed differing utilization strategies as revealed by coupling phospholipid fatty acid (PLFA) analysis with stable isotope techniques. Fungi assimilated C directly in the litter, whereas bacteria took up the substrates in the soil and therefore depended more on transport processes than fungi. Our results demonstrate the impact of physicochemical conditions on the abundance and function of microorganisms in the detritusphere. Furthermore, the combination of enzymatic measurements and mathematical transport modelling may offer a new way to measure substrate decay rates in soil.
In the Congo, near Pointe‐Noire,
The quantitative and qualitative evolution of the whole soil carbohydrates was studied as a function of plantation age. Carbohydrate‐C represents 131 mg g−1 of the soil organic carbon in the savanna soil, but decreases to an average value of 75 mg g−1 in plantations more than 6 years old. This appears to be due mainly to the stimulation of the mineralization of the glucose, which represented 60% of the total sugars in savanna soil and only 45–48% in tree plantations. The ratio [arabinose + galactose + fucose]/[rhamnose + xylose], which is the largest in the oldest plantations, is significant for evaluating the replacement of carbohydrates of the original grass savanna by those of the trees.
Soil from Eutrochrept A horizons under long‐term spruce forest (Sf), mixed deciduous forest (Df), permanent grassland (Gp) and arable rotation (Ar) was fractionated according to particle size and analysed for contents of C, N, lignin‐derived phenols and carbohydrates.
Whole soil from Sf, Df, Gp and Ar contained 84, 59, 73 and 25 g C kg−1 soil, respectively. For all sites, the C content declined and C/N ratio increased in the order: clay (<2 μm), silt (2–20 μm), sand (20–2000 μm). Clay and silt were significantly lower in C in Ar than in Sf, Df and Gp, C associated with sand being substantially lower under arable rotation.
The yield of lignin‐derived phenols decreased and carboxyl functionality and methoxyl demethylation of lignin derivatives increased with decreasing particle size, indicating a progressive lignin alteration. Whole soil from Sf and Gp was substantially higher in vanillyl (V), syringyl (S) and cinnamyl (C) units (VSC) than soil from Df and Ar. Compared to whole soil, clay was depleted and sand enriched in VSC. Only sand appeared to be affected significantly by land use. Sand from Ar and Df was more enriched in VSC than sand from Gp and Sf.
Whole soil carbohydrates decreased in the order: Gp>Ar>Df>Sf. Sand‐ and clay‐sized separates were enriched in carbohydrates compared to silt. Carbohydrates in sand were mainly of plant origin whereas microbially‐derived sugars accounted for a larger proportion in the clay. Compared to Sf, Df and Gp, clay from Ar was enriched and sand depleted in microbial sugars.
Lignin and carbohydrate distribution patterns indicate that organic matter was in a more advanced stage of decomposition in the sand separates from forest than from agricultural A horizons. The forest soils also show a higher degree of oxidative changes in lignin associated with clay. In contrast, differences between silt from the four A horizons were small.
Particulate organic matter (POM) is a labile fraction of soil organic matter which is thought to be physically protected from biodegradation when within soil aggregates. We have developed a fractionation method to separate POM located outside stable soil macroaggregates (> 200 μm) and microaggregates (50–200 μm) from that within them, and applied it to a cultivation sequence of humic loamy soils. The natural abundance of 13C was used to determine the amounts of POM derived from forest and that derived from crop in the free and occluded fractions. In the forest soil the free and occluded POM fractions had the same composition, morphology and isotopic signature. On cultivation the amounts of POM decreased sharply. The loss of C in the POM from forest was mainly from POM outside the aggregates. The POM occluded within microaggregates was found to turnover slowly. This may be due either to its recalcitrant chemical nature or to its physical protection within microaggregates
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