Transformation and binding of 13C and 14C-labelled atrazine in relation to straw decomposition in soil

As a source of organic matter, crop residues affect the behaviour of pesticides in agricultural soils. The fate of [U‐ring‐¹³C] and [U‐ring‐¹⁴C] atrazine (6‐chloro‐N‐ethyl‐N‐isopropyl‐1,3,5‐triazine‐2,4‐diamine) was investigated during laboratory incubation under controlled conditions in a loamy soil amended with wheat straw at two different states of decomposition: no preliminary decomposition or 6 months’ preliminary decomposition. After 3 months, non‐extractable, so‐called ‘bound’, ¹³C‐atrazine residues were recovered in three particle‐size fractions (> 200, 50–200 and < 50 μm), and investigated with solid‐state ¹³C‐NMR spectroscopy. Parallel incubations with [U‐ring‐¹⁴C] atrazine were carried out to quantify the bound residues as well as the extractable and mineralized fractions. The effect of straw residues on atrazine behaviour depended on whether they had been previously decomposed or not. When straw was decomposed for 6 months prior to incubation, atrazine mineralization was enhanced to 50% of the initial ¹⁴C in contrast to 15% of the initial ¹⁴C in soil alone and soil amended with fresh straw. In parallel, atrazine bound residues were formed in greater amount representing up to 20% of the initial ¹⁴C. CP/MAS ¹³C‐NMR on soil size fractions of soil–straw mixtures after incubation with ¹³C‐atrazine showed that bound residues contained mostly triazinic C, corresponding to atrazine or primary metabolites. Non‐humified organic materials recovered in size fractions > 200 and 50–200 μm contained significant amounts of bound residues, especially when straw was added to the soil. CP/MAS ¹³C‐NMR analysis of humic acids obtained from < 50‐μm fractions was difficult due to overlapping of the native carboxyl ¹³C signal with the ¹³C‐atrazine signal.     

Organic matter in density fractions of water-stable aggregates in silty soils: Effect of land use

The location of soil organic matter (SOM) within the soil matrix is considered a major factor determining its turnover, but quantitative information about the effects of land cover and land use on the distribution of SOM at the soil aggregate level is rare. We analyzed the effect of land cover/land use (spruce forest, grassland, wheat and maize) on the distribution of free particulate organic matter (POM) with a density <1.6 g cm⁻³ (free POM_<1.6), occluded particulate organic matter with densities <1.6 g cm⁻³ (occluded POM_<1.6) and 1.6-2.0 g cm⁻³ (occluded POM_1.6-2.0) and mineral-associated SOM (>2.0 g cm⁻³) in size classes of slaking-resistant aggregates (53-250, 250-1000, 1000-2000, >2000 μm) and in the sieve fraction <53 μm from silty soils by applying a combined aggregate size and density fractionation procedure. We also determined the turnover time of soil organic carbon (SOC) fractions at the aggregate level in the soil of the maize site using the ¹³C/¹²C isotope ratio. SOM contents were higher in the grassland soil aggregates than in those of the arable soils mainly because of greater contents of mineral-associated SOM. The contribution of occluded POM to total SOC in the A horizon aggregates was greater in the spruce soil (23-44%) than in the grassland (11%) and arable soils (19%). The mass and carbon content of both the free and occluded POM fractions were greater in the forest soil than in the grassland and arable soils. In all soils, the C/N ratios of soil fractions within each aggregate size class decreased in the following order: free POM_<1.6>occluded POM_<1.6-2.0>mineral-associated SOM. The mean age of SOC associated with the <53 μm mineral fraction of water-stable aggregates in the Ap horizon of the maize site varied between 63 and 69 yr in aggregates >250 μm, 76 yr in the 53-250 μm aggregate class, and 102 yr in the sieve fraction <53 μm. The mean age of SOC in the occluded POM increased with decreasing aggregate size from 20 to 30 yr in aggregates >1000 μm to 66 yr in aggregates <53 μm. Free POM had the most rapid rates of C-turnover, with residence times ranging from 10 yr in the fraction >2000 μm to 42 yr in the fraction 53-250 μm. Results indicated that SOM in slaking-resistant aggregates was not a homogeneous pool, but consisted of size/density fractions exhibiting different composition and stability. The properties of these fractions were influenced by the aggregate size. Land cover/land use were important factors controlling the amount and composition of SOM fractions at the aggregate level.     

Short-term kinetics of residual wheat straw C and N under field conditions: characterization by 13C15N tracing and soil particle size fractionation

Summary A clear understanding of the short-term decomposition and fate of crop residues is necessary to predict the availability of mineral N in soil. The fate of ¹³ C¹⁵N-labelled wheat straw in a silty soil (Typic Hapludalf) was studied using particle size fractionation and in situ incubation in which the equivalent of 8 t dry matter per ha of straw was incorporated into the soil over 574 days. Soil samples were separated into five particle-size fractions by wet sieving after disruption of aggregates. The weight, C and N contents, and ¹³C and ¹⁵N atom excess of each fraction were determined. Straw-derived C disappeared rapidly from the > 2000-μm fraction with an estimated half-life of 53 'normalized' days (equivalent of 10°C and −0−01 MPA water potential). Straw-derived C appeared to be only temporarily stored in the intermediate fractions (1000–2000 and 200–1000 pm). The maximum net ¹³C accumulation in the 50–200-μm fraction was 4·4% of added ¹³C. Straw-derived C accumulated most rapidly and preferentially in the 50-μm fraction, which stabilized after 265 days and accounted for 70% of the residual ¹³C on day 574. Although there was more residual ¹⁵N than ¹³C, the distributions and kinetics of the two isotopes in the fractions were similar.     

Fate of Carbon in Water-Stable Aggregates during Decomposition of 13C-Labeled Corn Straw

Fundamental knowledge about decomposition, fate of crop residue, and allocation of residue-derived carbon (C) in soil aggregates is essential to understand the C dynamics in soil. The incorporation of C derived from corn residue in water-stable aggregate fractions, particulate organic C (POC), and mineral-associated C (MAC) in soil were examined using the ¹³C tracer technique. Soil was treated with corn straw at the rate of 1% dry mass of soil brought to 66% of field capacity and incubated for 70 days at 25 °C. Samples were taken at 20, 35, and 70 days and analyzed for water-stable aggregates. Values for POC and MAC were analyzed for total C and ¹³C enrichment. The addition of corn straw caused a shift in the distribution of recoverable particles with significant decreases in <53-μm silts and clays, microaggregrates (53–250 μm), and smaller macroaggegates (250–2000 μm); however, the large macroaggegates (>2000 μm) increased significantly. Macroaggregates contained greater amount of C than microaggregates. The proportion of ¹³C recovered in the fractions <53 μm (silt and clay), 53–250 μm, and 250–2000 μm increased during decomposition of corn straw, whereas there was no significant change in >2000-μm fraction. Most (70–76%) of the soil organic C was affiliated with MAC (<53 μm). Carbon (¹³C) derived from corn straw decreased in POC but increased in MAC as decomposition proceeded. In the long term, microaggregate fraction appears to be involved in storage and stabilization of the C derived from corn straw and is important for soil quality and soil C sequestration point of view.     

The contribution from hyphae, roots and organic carbon constituents to the aggregation of a sandy loam under long-term clover-based and grass pastures

Water-stable macro-aggregate size fractions (>2.0 mm, 1.0–2.0 mm, 0.5–1.0 mm and 0.25–0.5 mm) and non-aggregated soil from a sandy loam under long-term clover-based pasture and from grass pasture were analysed to determine the role of acid- and water-extractable carbohydrate C, total hyphal length, microbial biomass, organic C and total and mycorrhizal root length in stabilization of the aggregates. Aggregates were examined by scanning electron microscopy (SEM) and the particle-size distribution of the size fractions was also determined. Macro-aggregation increased under grass, relative to clover-based pasture; however, the properties of the aggregate fractions measured did not reflect this difference. Microbial-biomass C, extractable-carbohydrate C, hyphal length, total and mycorrhizal root length and organic C content of the soils were poorly correlated with macro-aggregation. Within the aggregates, the proportion of 250–1000-km sand was smaller and clay, silt and fine sand (20–250 μm) were greater relative to non-aggregated soil, suggesting that the >250-μm sand in the non-aggregated soil limited the stabilization of macro-aggregates. Under SEM, no enmeshment of aggregates by hyphae and roots was apparent. Although 50–160 m hyphae g^?1 soil was found within the aggregates, calculations showed that on average only 5 to 13 lengths of hyphae were associated with each 250-μm cube of soil within the aggregates, and suggested little potential to stabilize the aggregates by enmeshing. On average, all >2.0-mm aggregates contained less than 3.6 mm of roots and less than 50% by weight of <2.0-mm aggregates contained a single length of root. The findings cast doubt about the role of hyphae and fine roots in the stabilization of macro-aggregates through an enmeshing mechanism in sandy soils.     

Following the decomposition of ryegrass labelled with 13C and 15N in soil by solid-state nuclear magnetic resonance spectroscopy

Investigating the biogeochemistry of plant material decomposition in soil has been restricted by difficulties extracting and identifying organic compounds. In this study the decomposition of ¹³C- and ¹⁵N-labelled Lolium perenne leaves mixed with mineral soil has been investigated over 224 days of incubation under laboratory conditions. Decomposition was followed using short-term rates of CO₂ evolution, the amounts of ¹³C and ¹⁵N remaining were determined by mass spectrometry, and ¹³C and ¹⁵N solid-state nuclear magnetic resonance (NMR) spectroscopy was used to characterize chemically the plant material as it decomposed. After 224 days 48% of the added ¹³C had been lost with a rapid period of C0₂ evolution over the first 56 days. The fraction of cross-polarization magic angle spinning (CP MAS) ¹³C NMR spectra represented by O-alkyl-C signal probably in carbohydrates (chemical shift, 60–90 p.p.m.) declined from 60 to 20% of the spectrum (chemical shift, 0–200 p.p.m.) over 224 days. The rate of decline of the total ¹³C exceeded that of the 60–90 p.p.m. signal during the first 56 days and was similar thereafter. The fraction of the CP MAS ¹³C NMR spectra represented by the alkyl- and methyl-C (chemical shift, 10–45 p.p.m.) signal increased from 5 to 14% over the first 14 days and was 19% after 224 days. CP MAS ¹³C NMR of ¹³C- and ¹⁵N-L. perenne contained in 100-μm aperture mesh bags incubated in the soil for 56 days indicated that the remaining material was mainly carbohydrate but there was an increase in the alkyl- and methyl-C associated with the bag's contents. After 224 days incubation of the labelled ¹³C- and ¹⁵N-L. perenne mixed with the soil, 40% of the added N had been lost. Throughout the incubation there was only one signal centred around 100 p.p.m. detectable in the CP MAS ¹⁵N NMR spectra. This signal corresponded to amide ¹⁵N in peptides and may have been of plant or microbial origin or both. Although there had been substantial interaction between the added ¹⁵N and the soil microorganisms, the associated redistribution of ¹⁵N from plant to microbial tissues occurred within the amide region. The feasibility of following some of the component processes of plant material decomposition in soil using NMR has been demonstrated in this study and evidence that microbial synthesis contributes to the increase in alkyl- and methyl-C content of soil during decomposition has been represented.     

How do earthworms influence organic matter quantity and quality in tropical soils?

Earthworms are important regulators of soil structure and soil organic matter (SOM) dynamics; however, quantifying their influence on SOM cycling in tropical ecosystems remains little studied. Simulated rainfall was used to disrupt casts produced by Amynthas khami and their surrounding soil (control) into a range of small sized aggregates (50-250, 250-500, 500-2000 and 2000-5000 μm). To gain insight into how earthworms influence SOM biogeochemical composition in the aggregates, we carried out elemental and stable isotope analysis, and analytical pyrolysis (Py GC/MS). We also characterized their lignin component after oxidation with cupric oxide (CuO).The C content of smaller size fractions (<500 μm) in the control soil was higher than in the larger fractions. Our study therefore suggests that the aggregate hierarchy concept, which is used to understand soil aggregates and SOM dynamics in temperate soils, may not be applicable to the tropical Acrisol studied here. Earthworms modified SOM organization in soil aggregates. Although the isotope analyses were useful for highlighting SOM enrichment in the earthworm casts, aggregate fractions could not be classified according to particle size. Molecular analyses were necessary to indicate that SOM in all size fractions of casts consisted of relatively undecomposed material. Protection of the most labile SOM structures occurred in the smallest aggregate size fraction (50-250 μm). Py GC/MS showed that earthworm casts and control aggregates <2000 μm could be clearly distinguished according to the molecular properties of their SOM. Aggregates larger than 2000 μm, however, were most probably composed of all fractions and were not different. As a consequence, our results indicate that studies to determine the impact of earthworms on SOM turnover in soil are spatially dependant on the scale of observation.     

Effect of litter quality and soil fungi on macroaggregate dynamics and associated partitioning of litter carbon and nitrogen

We investigated the effect of plant residue decomposability and fungal biomass on the dynamics of macroaggregate (250–2000 μm) formation in a three months' incubation experiment and determined the distribution of residue-derived C and N in the microbial biomass and in aggregate size fractions (250–2000 μm, 53–250 μm and <53 μm) using ¹³C and ¹⁵N data. A silty loam soil (sieved <250 μm) was incubated with and without addition of ¹⁵N labelled maize leaves (C/N = 27.4) and roots (C/N = 86.4). Each treatment was carried out with and without fungicide application. The addition of maize residues enhanced soil respiration and microbial biomass C and N and resulted in increased macroaggregate formation with a higher and more rapid maximum macroaggregation in the soil amended with maize leaves than in that with addition of roots. Fungicide application led to a significant decline of microbial biomass C and mineralization of the added residues compared to untreated soils, which demonstrates a successful suppression of part of the active microbial biomass by the fungicide. However, this was not confirmed by a generally lower ergosterol concentration. Consequently, ergosterol was no reliable fungal biomarker in periods of rapid decline of the fungal biomass. A single addition of fungicide was insufficient for continued inhibition of the fungal biomass. Yet, a significant delay (28–42 days) in macroaggregation in fungicide treated compared to untreated samples highlighted the importance of the fungal biomass in macroaggregate formation. Macroaggregates were enriched in maize-derived ¹³C and ¹⁵N compared to microaggregates or the fraction < 53 μm. They turned over rapidly with decreasing substrate availability, which entailed a transfer of maize-derived C and N stored within macroaggregates during the first weeks of incubation to microaggregates with proceeding incubation time. Our results indicate that this transfer happened within macroaggregates, because no considerable amount of free particulate organic matter (POM) was released upon macroaggregate breakdown. We conclude that substrate decomposability and fungal activity are key factors determining extent and dynamics of macroaggregation during decomposition processes. Macroaggregate formation implied rapid incorporation and thereby short-term protection of maize-derived C and N. Moreover, macroaggregates allowed a transfer of maize-derived organic matter into microaggregates within macroaggregates, which prevented the release of significant amounts of free POM upon macroaggregate breakdown. Consequently, macroaggregates constitute to the transfer of recently added C into more stable soil organic matter fractions.     

Organic matter turnover in soil physical fractions following woody plant invasion of grassland: Evidence from natural C and N

Soil physical structure causes differential accessibility of soil organic carbon (SOC) to decomposer organisms and is an important determinant of SOC storage and turnover. Techniques for physical fractionation of soil organic matter in conjunction with isotopic analyses (δ¹³C, δ¹⁵N) of those soil fractions have been used previously to (a) determine where organic C is stored relative to aggregate structure, (b) identify sources of SOC, (c) quantify turnover rates of SOC in specific soil fractions, and (d) evaluate organic matter quality. We used these two complementary approaches to characterize soil C storage and dynamics in the Rio Grande Plains of southern Texas where C₃ trees/shrubs (δ¹³C=−27‰) have largely replaced C₄ grasslands (δ¹³C=−14‰) over the past 100-200 years. Using a chronosequence approach, soils were collected from remnant grasslands (Time 0) and from woody plant stands ranging in age from 10 to 130 years. We separated soil organic matter into specific size/density fractions and determined their C and N concentrations and natural δ¹³C and δ¹⁵N values. Mean residence times (MRTs) of soil fractions were calculated based on changes in their δ¹³C with time after woody encroachment. The shortest MRTs (average=30 years) were associated with all particulate organic matter (POM) fractions not protected within aggregates. Fine POM (53-250 μm) within macro- and microaggregates was relatively more protected from decay, with an average MRT of 60 years. All silt+clay fractions had the longest MRTs (average=360 years) regardless of whether they were found inside or outside of aggregate structure. δ¹⁵N values of soil physical fractions were positively correlated with MRTs of the same fractions, suggesting that higher δ¹⁵N values reflect an increased degree of humification. Increased soil C and N pools in wooded areas were due to both the retention of older C₄-derived organic matter by protection within microaggregates and association with silt+clay, and the accumulation of new C₃-derived organic matter in macroaggregates and POM fractions.     

Glucose additions to aggregates subjected to drying/wetting cycles promote carbon sequestration and aggregate stability

Biogeochemical mechanisms at microscale regions within soil macroaggregates strengthen aggregates during repeated DW cycles. Knowledge of additional biogeochemical processes that promote the movement of dissolved organic carbon (DOC) into and throughout soil aggregates and soil aggregate stabilization are essential before we can more accurately predict maximum carbon (C) sequestration by soils subjected to best management practices. We investigated the spatial distribution of ¹³C-glucose supplied to individual soil macroaggregate surfaces and subjected to multiple drying and wetting (DW) cycles. Subsequent distribution of added glucose-C, CO₂ respiration, increased microbial community activity and concomitant changes in soil aggregate stabilization were monitored. Moist macroaggregates were treated with no DW cycles and zero glucose C (Control), 5 DW cycles and zero glucose (DW0G), and 5 DW cycles with additions of 250 μg glucose-¹³C/g soil during each cycle (DW+G). Repeated additions of glucose-C to aggregate surfaces reduced the mineralization of pre-existing soil C by an average of 45% and established concentric gradients of glucose-derived C. It is concluded these increasing gradients promoted the diffusion of soluble C into interior regions and became less available to microbial respiration. Spatial gradients of glucose-derived C within aggregates influenced a shift in the abundance of unique ribotypes spatially distributed within aggregates. Rapid decreases in the mineralization rates of glucose-C during repeated DW cycles suggested greater C sequestration by either physical restriction of microbes or chemical sorption of new C that diffused into aggregates. Aggregate stability decreased significantly following 2-3 DW cycles, when glucose-C was not added. Additions of glucose-C with each DW cycle maintained soil aggregate stability equal to the moist but not cycled control throughout the 5 DW cycles of this study. These data simulate the strengthening of soil aggregates in no tillage agroecosystems which provides continuous additions of DOC compounds generated by decomposing plant residues on the soil surface, and root exudates and decomposition, as well as the mineralization of POM materials within nondisturbed soil profiles.     

Distribution and availability of fungicide-derived copper in soil aggregates

Purpose

Soil consists of various sizes of aggregates, and different soil aggregates vary in their abilities to adsorb or transport metals. This study aimed to investigate the distribution behaviors of Cu from different fungicides in soil aggregates after a 15-month incubation.

Materials and methods

Bordeaux mixture (CuSO₄/Ca(OH)₂?=?1/1 by weight, BR), copper nitrate (Cu(NO₃)₂·4H₂O, CN), and copper oxychloride (3Cu(OH)₂·CuCl₂, CO) were applied to a representative Chinese Mollisol to reach the Cu content 200 mg kg^?1. Five soil aggregate fractions, i.e., >?2000 μm, 2000–1000 μm, 1000–500 μm, 500–250 μm, and <?250 μm, were obtained by the wet sieving method. The modified Bureau Communautaire de Références (BCR) sequential extraction was applied to assess the Cu distribution among the main soil fractions.

Results and discussion

The highest Cu mass loading was found for the >?2000-μm soil aggregate. The input Cu was mainly in stable fractions, and the highest proportion was found for the residual fraction. The bioavailability and mobility of Cu from different fungicides in soils varied from each other, and they presented an order of CO > CN > BR. High bioavailability and transferring coefficients were found in the <?250-μm and >?2000-μm soil aggregates.

Conclusions

This study indicated that the input Cu from fungicides mainly distributed in the >?2000-μm soil aggregates. Moreover, the CO-derived Cu presented a higher availability than the BR- and CN-derived Cu in the soil.

     

Soil Na+ concentration controls salt-affected soil organic matter components in Hetao region China

Purpose

There is little knowledge on the organic matter fractions of salt-affected soil aggregates. This study aimed at investigating characteristics of salt-affected soil organic carbon components and the relationships between soil salt concentration and soil organic carbon component content.

Materials and methods

Five typical salt-affected soils in Hetao region China were collected and analyzed for light (LF) and heavy fraction (HF) in different water-stable aggregates. And the soil organic carbon components were measured by Fourier transform infrared (FTIR) and pyrolysis-gas chromatography/mass spectrometer (Py–GC/MS).

Results and discussion

The results showed that the salt-affected soils were dominant in 53–10-μm water-stable aggregates, 61–80% in the bulk soil, and very low in >?250-μm macro-aggregates, less than 7.06% in the bulk soil. The proportions of >?250-μm macro-aggregates and the mean weight diameter (MWD) were negatively correlated to Na⁺ concentration (p?<?0.05). Furthermore, the macro-aggregates were generally higher in total organic carbon (TOC) and accordingly higher C/N ratio than those in micro-aggregates. Heavy fractions (HF) from both >?53 μm and <?53-μm soil aggregates accounted for 99.30–99.83% of the bulk soil and contained 89.6–98.5% lower TOC and accordingly 49.2–84.8% lower C/N ratio than those in light fractions (LF). The LFs were high in lignin (7.27–34.02% in total pyrolysis products, 19.89% on average) and alkane/alkene-derived compounds (9.51–37.21%, 23.18% on average), but low in N-containing compounds (0–3.64%, 1.71% on average), while HFs were high in both alkane/alkene (4.38–27.46%, 15.06% on average) and N-containing compounds (7.45–26.45%, 13.98% on average), but low in lignin-derived compounds (1.13–8.75%, 3.86% on average).

Conclusions

The tested salt-affected soils were predominant in 53–10-μm micro-aggregates, which was caused by the Na⁺ dispersion effect on soil aggregates. Most SOM was stored in HF that contained high N-containing compounds and low C/N ratios. Our results suggested that the components of SOM were mainly controlled by the soil Na⁺ concentration.

     

Protection of soil carbon by microaggregates within earthworm casts

Earthworms are known to play a role in aggregate formation and soil organic matter (SOM) protection. However, it is still unclear at what scale and how quickly earthworms manage to protect SOM. We investigated the effects of Aporrectodea caliginosa on aggregation and aggregate-associated C pools using ¹³C-labeled sorghum (Sorghum bicolor (L.) Moench) leaf residue. Two incubations were set up. The first incubation consisted of soil samples crushed <250 μm to break up all macroaggregates with three treatments: (i) control soil; (ii) soil+¹³C-labeled residue and (iii) soil+¹³C-labeled residue+earthworms. Earthworms were added after 8 d and 12 d (days) later, aggregate size distribution was measured together with total C and ¹³C in each aggregate fraction. A second incubation was made to assay protected versus unprotected total C and ¹³C from 21-d laboratory incubations of intact and crushed large (>2000 μm) and small (250-2000 μm) macroaggregates and microaggregates (53-250 μm). Eight different pools of aggregate-associated C were quantified: (1) and (2) unprotected C pools in large and small macroaggregates, (3) unprotected C pools in microaggregates, (4) and (5) protected C pools in large and small macroaggregates, (6) protected C pool in microaggregates, and (7) and (8) protected C pools in microaggregates within large and small macroaggregates. In the presence of earthworms, a higher proportion of large macroaggregates was newly formed and these aggregates contained more C and ¹³C compared to bulk soil. There were no significant differences between the samples with or without earthworms in the C pool-sizes protected by macroaggregates, microaggregates or microaggregates within small macroaggregates. However, in the presence of earthworms, the C protected by microaggregates within large macroaggregates was a significant pool and 22% of this C pool was newly added C. In conclusion, these results clearly indicate the direct involvement of earthworms in providing protection of soil C in microaggregates within large macroaggregates leading to a possible long-term stabilization of soil C.     

Decomposition of 15N-labelled catch-crop residues in soil: evaluation of N mineralization and plant-N uptake potentials under controlled conditions

The decomposition of ¹⁵N-labelled catch-crop materials (rape, radish and rye), obtained from field experiments, was studied in a chalky Champagne soil during a 60-week incubation at 28°C. Mineralized N was assumed to come from either labile or recalcitrant fractions of plant residues. The labile fraction represented about one-third of the catch-crop N; its mineralization rate constant varied from 0.06 to 0.12 d^?1. The decomposition rate of the recalcitrant N fraction ranged from 0.03 × 10^?2 to 0.06 × 10^?2 d^?1. Catch-crop species and rate of incorporation had no effect on N residue mineralized at the end of incubation. The decomposition of labelled rye was monitored in the same soil during a 5-month pot experiment to determine the N availability to an Italian ryegrass crop and the effect of plants on the decomposition processes. The ¹⁵N-rye decomposed rapidly both in the presence or absence of Italian ryegrass, but the amounts of N mineralized were influenced by the presence of living roots: 42% of the ¹⁵N in labelled rye was present as inorganic N in the pots without plants after 5 months, compared with only 32% in the ryegrass crop. Comparison of microbial-biomass dynamics in both treatments suggested that there had been preferential utilization by soil micro-organisms of materials released from the living roots than the labelled plant residues.     

Earthworm impacts on soil organic matter and fertilizer dynamics in tropical hillside agroecosystems of Honduras

Earthworms are important processors of soil organic matter (SOM) and nutrient turnover in terrestrial ecosystems. In agroecosystems, they are often seen as beneficial organisms to crop growth and are actively promoted by farmers and extension agents, yet their contribution to agroecosystem services is uncertain and depends largely on management. The Quesungual slash-and-mulch agroforestry system (QSMAS) of western Honduras has been proposed as a viable alternative to traditional slash-and-burn (SB) practices and has been shown to increase earthworm populations, yet the effect of earthworms on soil fertility and SOM in QSMAS is poorly understood. This study examined the role of Pontoscolex corethrurus in QSMAS by comparing their influence on aggregate-associated SOM and fertilizer dynamics with their effects under SB and secondary forest in a replicated field trial. Both the fertilized QSMAS and SB treatments had plots receiving additions of inorganic ¹⁵N and P, as well as plots with no inorganic N additions. Earthworm populations were manipulated in field microcosms at the beginning of the rainy season within each management treatment via additions of P. corethrurus or complete removal of existing earthworm populations. Microcosms were destructively sampled at harvest of Zea mays and soils were wet-sieved (using 53, 250 and 2000 μm mesh sizes) to isolate different aggregate size fractions, which were analyzed for total C, N and ¹⁵N. The effects of management system were smaller than expected, likely due to disturbance associated with the microcosm installation. Contrary to our hypothesis that earthworms would stabilize organic matter in soil aggregates, P. corethrurus decreased total soil C by 3% in the surface layer (0-15 cm), predominantly through a decrease in the C concentration of macroaggregates (>250 μm) and a corresponding depletion of C in coarse particulate organic matter occluded within macroaggregates. Earthworms also decreased bulk density by over 4%, but had no effect on aggregate size distribution. Within the two fertilized treatments, the QSMAS appeared to retain slightly more fertilizer derived N in smaller aggregate fractions (<250 μm) than did SB, while earthworms greatly reduced the recovery of fertilizer N (34% decrease) in both systems. Although management system did not appear to influence the impact of P. corethrurus on SOM or nutrient dynamics, we suggest the lack of differences may be due to artificially low inputs of fresh residue C to microcosms within all management treatments. Our findings highlight the potential for P. corethrurus to have deleterious impacts on soil C and fertilizer N dynamics, and emphasize the need to fully consider the activities of soil fauna when evaluating agroecosystem management options.     

C and N in soil organic matter density fractions under elevated atmospheric CO2: Turnover vs. stabilization

Turnover of C and N in an arable soil under Free Air Carbon Dioxide (FACE) experiment was studied by the use of ¹³C natural abundance and ¹⁵N-labeled fertilizers. Wheat was kept four growing seasons under ambient and elevated CO₂ concentrations and fertilized for three growing seasons. Density fractionation of soil organic matter (SOM) allowed to track ¹³C and ¹⁵N in free particulate organic matter (fPOM; <1.6 g cm⁻³), particulate organic matter occluded within aggregates with two densities (oPOM 1.6, oPOM 1.6-2.0 g cm⁻³), and in mineral-associated organic matter (>2.0 g cm⁻³) fractions. Elevated CO₂ and N fertilization did not significantly affect C and N contents in the bulk soil. Calculated mean residence time (MRT) of C and N revealed the qualitative differences of SOM density fractions: (i) the shortest MRT_C and MRT_N in fPOM confirmed high availability of this fraction to decomposition. Larger C/N ratio of fPOM under elevated vs. ambient CO₂ indicated an increasing recalcitrance of FACE-derived plant residues. (ii) There was no difference in MRT of C and N between lighter and heavier oPOMs probably due to short turnover time of soil aggregates which led to oPOM mixing. The increase of MRT_C and MRT_N in both oPOMs during the experiment confirmed the progressive degradation of organic material within aggregates. (iii) Constant turnover rates of C in the mineral fraction neither confirmed nor rejected the assumed stabilization of SOM to take place in the mineral fraction. Moreover, a trend of decreasing of C and N amounts in the Min fraction throughout the experiment was especially pronounced for C under elevated CO₂. Hence, along with the progressive increase of C_FACE in the Min fraction the overall losses of C under elevated CO₂ may occur at the expense of older “pre-FACE” C.     

Microbial biomass formed from 14C, 15N-labelled plant material decomposing in soils in the field

The decomposition of ¹⁴C, ¹⁴N-labelled medic (Medicago littoralis) material and the net formation and decay of isotope-labelled biomass have been measured in four South Australian soils in the field over 4 yr. The field sites were in similar climatic zones but two sites received about twice as much rainfall as the others. The soils were calcareous and of similar pH, but differed in texture and organic matter content. The decomposition of the organic-¹⁴C and organic-¹⁵N residues were, for a given site, similar. Initially, the concentrations of labelled residues decreased rapidly, then very slowly. Decomposition rates in a heavy clay soil were significantly less than in the other soils during the first 16 weeks after incorporation of plant material, but thereafter, rates of decomposition in all soils were similar, despite differences in soil texture and climate. More than 50% of the medic-¹⁴C had disappeared from all soils after 4 weeks of decomposition and only 15–20% of the medic-¹⁴C remained as organic residues after 4 yr. Of the medic-¹⁵N 60–65% remained as organic residues after 32 weeks decomposition; the percentage decreased to 45–50% after 4 yr.The amounts of ¹⁴C, ¹⁴N-labelled biomass, formed from decomposing plant material, were maximal 4–8 weeks after incorporation of plant material into the soils. In samples taken at 8 weeks from the sandy Roseworthy soil, biomass-¹⁴C and -¹⁵N accounted for 14 and 22% respectively of the total organic-¹⁴C and -¹⁵N residues present. Thereafter in this soil, the concentrations of biomass-¹⁴C and -¹⁵N decreased, rapidly at first then more slowly. Nevertheless, throughout most of the decomposition the rates of decrease in the concentrations of biomass-¹⁴C and -¹⁵N exceeded those of the non-biomass, labelled organic residues.The proportions of ¹⁴C, ¹⁵N-labelled materials accounted for in the labelled biomass varied between soils. Soils of higher clay content generally retained higher proportions of residual organic-¹⁴C and -¹⁴N in the biomass, even though the net rates of decomposition of total labelled residues did not differ significantly between soils during most of the decomposition.     

Transformation of organic matter from maize residues into labile and humic fractions of three European soils as revealed by 13C distribution and CPMAS-NMR spectra

The dynamics of incorporation of fresh organic residues into the various fractions of soil organic matter have yet to be clarified in terms of chemical structures and mechanisms involved. We studied by ¹³C‐dilution analysis and CPMAS‐¹³C‐NMR spectroscopy the distribution of organic carbon from mixed or mulched maize residues into specific defined fractions such as carbohydrates and humic fractions isolated by selective extractants in a year‐long incubation of three European soils. The contents of carbohydrates in soil particle size fractions and relative δ¹³C values showed no retention of carbohydrates from maize but rather decomposition of those from native organic matter in the soil. By contrast, CPMAS‐¹³C‐NMR spectra of humic (HA) and fulvic acids (FA) extracted by alkaline solution generally indicated the transfer of maize C (mostly carbohydrates and peptides) into humic materials, whereas spectra of organic matter extracted with an acetone solution (HE) indicated solubilization of an aliphatic‐rich, hydrophobic fraction that seemed not to contain any C from maize. The abundance of ¹³C showed that all humic fractions behaved as a sink for C from maize residues but the FA fraction was related to the turnover of fresh organic matter more than the HA. Removal of hydrophobic components from incubated soils by acetone solution allowed a subsequent extraction of HA and, especially, FA still containing much C from maize. The combination of isotopic measurements and NMR spectra indicated that while hydrophilic compounds from maize were retained in HA and FA, hydrophobic components in the HE fraction had chemical features similar to those of humin. Our results show that the organic compounds released in soils by mineralization of fresh plant residues are stored mainly in the hydrophilic fraction of humic substances which are, in turn, stabilized against microbial degradation by the most hydrophobic humic matter. Our findings suggest that native soil humic substances contribute to the accumulation of new organic matter in soils.     

Reciprocal transfer of carbon and nitrogen by decomposer fungi at the soil-litter interface

We have investigated whether decomposer fungi translocate litter-derived C into the underlying soil while simultaneously translocating soil-derived inorganic N up into the litter layer. We also located and quantified where the translocated C is deposited within the soil aggregate structure. When ¹³C-labeled wheat straw was decomposed on the surface of soil amended with ¹⁵N-labeled inorganic N, we found that C and N were reciprocally transferred by fungi, with a significant quantity (121-151 μg C g⁻¹ whole soil) of litter-derived C being deposited into newly formed macroaggregates (>250 μm sized aggregates). Fungal inhibition reduced fungal biomass and the bidirectional C and N flux by approximately 50%. The amount of litter-derived C found in macroaggregates was positively correlated with litter-associated fungal biomass. This fungal-mediated litter-to-soil C transfer, which to our knowledge has not been demonstrated before for saprophytic fungi, may represent an important mechanism by which litter C enters the soil and becomes stabilized as soil organic matter within the macroaggregate structure.     

Biochar addition drives soil aggregation and carbon sequestration in aggregate fractions from an intensive agricultural system

Purpose

Biochar application is deemed to modify soil properties, but current research has been mostly conducted on the degraded land in tropical regions. Using six consecutive years of biochar field trial, we investigated effects of biochar on soil aggregates, structural stability, and soil organic carbon (SOC) and black C (BC) concentrations in aggregate fractions. The findings have important implications in managing soil structure and SOC sequestration in high fertility soils of the temperate areas.

Materials and methods

The study had four treatments: control; biochar rate at 4.5 (B4.5) and biochar rate at 9.0 t ha^?1 year^?1 (B9.0); and straw return (SR). Soil samples were collected from 0–10-cm layer, and aggregate size distribution was determined with the wet-sieving method. Then, the mean weight diameter (MWD) of aggregates and the aggregate ratio (AR), i.e., the ratio of the >250 μm to the 53–250 μm size were calculated to assess the structural stability. Total SOC and BC concentrations in bulk soil (<2 mm) and separated fractions (i.e., >2000, 250–2000, 53–250, and <53 μm) were measured.

Results and discussion

The B4.5 and B9.0 significantly increased macroaggregate (250–2000 μm) and MWD and AR indices relative to the control. Comparing to the SR, the improvements in soil aggregation under biochar treatments were limited. Additionally, more SOC in larger fractions (>2000, 250–2000, and 53–250 μm) and BC in extracted fractions under biochar soils were observed. These results implied that biochar addition enhanced both native SOC and BC physical protection by aggregation.

Conclusions

Biochar application is effective in mediating soil aggregation, and thus improves both native SOC and BC stabilization in an intensive cropping system of North China.