Long-term fertilization suppresses rice pathogens by microbial volatile compounds.

Microbial volatile organic compounds (VOCs) can suppress plant pathogens. Although fertilization strongly affects soil microbial communities, the influence of fertilization on microbial VOC-mediated suppression of pathogens has not been elucidated. Soil was sampled from a paddy field that had been subjected to the following treatments for 30 years: a no-fertilizer control, mineral fertilization (NPK), NPK combined with rice straw (NPK + S), NPK combined with chicken manure (70% NPK + 30% M). Then, within a laboratory experiment, pathogens were exposed to VOCs without physical contact to assess the impact of VOCs emitted from paddy soils on in vitro growth of the fungal rice pathogens: Pyricularia oryzae and Rhizoctonia solani. The VOCs emitted from soil reduced the mycelial biomass of P. oryzae and R. solani by 36-51% and 10-30%, respectively, compared to that of the control (no soil; no VOCs emission). Overall, the highest suppression of P. oryzae and R. solani was in the NPK and NPK + S soils, which emitted more quinones, phenols, and low alcohols than NPK + M soils. The abundances of quinones and phenols in the soil air were maximal in the NPK-fertilized soil because the low ratio of dissolved organic carbon and Olsen-P increased the population of key species such as Acidobacteriae, Anaerolineae, and Entorrhizomycetes. The abundance of alcohols was minimum in the NPK + S fertilized soil because the high SOC content decreased the population of Sordariomycetes. In conclusion, mineral fertilization affects bacterial and fungal VOC emissions, thereby suppressing the growth of R. solani and P. oryzae.

Visualization and quantification of carbon "rusty sink" by rice root iron plaque: Mechanisms, functions, and global implications.

Paddies contain 78% higher organic carbon (C) stocks than adjacent upland soils, and iron (Fe) plaque formation on rice roots is one of the mechanisms that traps C. The process sequence, extent and global relevance of this C stabilization mechanism under oxic/anoxic conditions remains unclear. We quantified and localized the contribution of Fe plaque to organic matter stabilization in a microoxic area (rice rhizosphere) and evaluated roles of this C trap for global C sequestration in paddy soils. Visualization and localization of pH by imaging with planar optodes, enzyme activities by zymography, and root exudation by 14 C imaging, as well as upscale modeling enabled linkage of three groups of rhizosphere processes that are responsible for C stabilization from the micro- (root) to the macro- (ecosystem) levels. The 14 C activity in soil (reflecting stabilization of rhizodeposits) with Fe2+ addition was 1.4-1.5 times higher than that in the control and phosphate addition soils. Perfect co-localization of the hotspots of ß-glucosidase activity (by zymography) with root exudation (14 C) showed that labile C and high enzyme activities were localized within Fe plaques. Fe2+ addition to soil and its microbial oxidation to Fe3+ by radial oxygen release from rice roots increased Fe plaque (Fe3+ ) formation by 1.7-2.5 times. The C amounts trapped by Fe plaque increased by 1.1 times after Fe2+ addition. Therefore, Fe plaque formed from amorphous and complex Fe (oxyhydr)oxides on the root surface act as a "rusty sink" for organic matter. Considering the area of coverage of paddy soils globally, upscaling by model revealed the radial oxygen loss from roots and bacterial Fe oxidation may trap up to 130 Mg C in Fe plaques per rice season. This represents an important annual surplus of new and stable C to the existing C pool under long-term rice cropping.

Metagenomic and 14 C tracing evidence for autotrophic microbial CO2 fixation in paddy soils.

Autotrophic carbon dioxide (CO2 ) fixation by microbes is ubiquitous in the environment and potentially contributes to the soil organic carbon (SOC) pool. However, the multiple autotrophic pathways of microbial carbon assimilation and fixation in paddy soils remain poorly characterized. In this study, we combine metagenomic analysis with 14 C-labelling to investigate all known autotrophic pathways and CO2 assimilation mechanisms in five typical paddy soils from southern China. Marker genes of six autotrophic pathways are detected in all soil samples, which are dominated by the cbbL genes (67%-82%) coding the ribulose-bisphosphate carboxylase large chain in the Calvin cycle. These marker genes are associated with a broad range of phototrophic and chemotrophic genera. Significant amounts of 14 C-CO2 are assimilated into SOC (74.3-175.8 mg 14 C kg-1 ) and microbial biomass (5.2-24.1 mg 14 C kg-1 ) after 45 days incubation, where more than 70% of 14 C-SOC was concentrated in the relatively stable humin fractions. These results show that paddy soil microbes contain the genetic potential for autotrophic carbon fixation spreading over broad taxonomic ranges, and can incorporate atmospheric carbon into organic components, which ultimately contribute to the stable SOC pool.

T4-like Phages Reveal the Potential Role of Viruses in Soil Organic Matter Mineralization.

Viruses are the most abundant biological entities in the world, but their ecological functions in soil are virtually unknown. We hypothesized that greater abundance of T4-like phages will increase bacterial death and thereby suppress soil organic carbon (SOC) mineralization. A range of phage and bacterial abundances were established in sterilized soil by reinoculation with 10-3 and 10-6 dilutions of suspensions of unsterilized soil. The total and viable 16S rRNA gene abundance (a universal marker for bacteria) was measured by qPCR to determine bacterial abundance, with propidium monoazide (PMA) preapplication to eliminate DNA from non-viable cells. Abundance of the g23 marker gene was used to quantify T4-like phages. A close negative correlation between g23 abundance and viable 16S rRNA gene abundance was observed. High abundance of g23 led to lower viable ratios for bacteria, which suggested that phages drove microbial necromass production. The CO2 efflux from soil increased with bacterial abundance but decreased with higher abundance of T4-like phages. Elimination of extracellular DNA by PMA strengthened the relationship between CO2 efflux and bacterial abundance, suggesting that SOC mineralization by bacteria is strongly reduced by the T4-like phages. A random forest model revealed that abundance of T4-like phages and the abundance ratio of T4-like phages to bacteria are better predictors of SOC mineralization (measured as CO2 efflux) than bacterial abundance. Our study provides experimental evidence of phages' role in organic matter turnover in soil: they can retard SOC decomposition but accelerate bacterial turnover.

Abundance and Diversity of CO2-Assimilating Bacteria and Algae Within Red Agricultural Soils Are Modulated by Changing Management Practice.

Elucidating the biodiversity of CO(2)-assimilating bacterial and algal communities in soils is important for obtaining a mechanistic view of terrestrial carbon sinks operating at global scales. "Red" acidic soils (Orthic Acrisols) cover large geographic areas and are subject to a range of management practices, which may alter the balance between carbon dioxide production and assimilation through changes in microbial CO(2)-assimilating populations. Here, we determined the abundance and diversity of CO(2)-assimilating bacteria and algae in acidic soils using quantitative PCR and terminal restriction fragment length polymorphism (T-RFLP) of the cbbL gene, which encodes the key CO(2) assimilation enzyme (ribulose-1,5-bisphosphate carboxylase/oxygenase) in the Calvin cycle. Within the framework of a long-term experiment (Taoyuan Agro-ecosystem, subtropical China), paddy rice fields were converted in 1995 to four alternative land management regimes: natural forest (NF), paddy rice (PR), maize crops (CL), and tea plantations (TP). In 2012 (17 years after land use transformation), we collected and analyzed the soils from fields under the original and converted land management regimes. Our results indicated that fields under the PR soil management system harbored the greatest abundance of cbbL copies (4.33 × 10(8) copies g(-1) soil). More than a decade after converting PR soils to natural, rotation, and perennial management systems, a decline in both the diversity and abundance of cbbL-harboring bacteria and algae was recorded. The lowest abundance of bacteria (0.98 × 10(8) copies g(-1) soil) and algae (0.23 × 10(6) copies g(-1) soil) was observed for TP soils. When converting PR soil management to alternative management systems (i.e., NF, CL, and TP), soil edaphic factors (soil organic carbon and total nitrogen content) were the major determinants of bacterial autotrophic cbbL gene diversity. In contrast, soil phosphorus concentration was the major regulator of algal cbbL community composition. Our results provide new insights into the diversity, abundance, and modulation of organisms responsible for microbial autotrophic CO(2) fixation in red acidic soils subjected to changing management regimes.

In situ simultaneous measuring method for the determination of key processes of soil organic carbon cycling: Soil microbial respiration using laser spectrometry.

RATIONALE: Soil microbial heterotrophic C-CO2 respiration is important for C cycling. Soil CO2 differentiation and quantification are vital for understanding soil C cycling and CO2 emission mitigation. Presently, soil microbial respiration (SR) quantification models are based on native soil organic matter (SOM) and require consistent monitoring of δ13C and CO2. METHODS: We present a new apparatus for achieving in situ soil static chamber incubation and simultaneous CO2 and δ13C monitoring by cavity ring-down spectroscopy (CRDS) coupled with a soil culture and gas introduction module (SCGIM) with multi-channel. After a meticulous five-point inter-calibration, the repeatability of CO2 and δ13C values by using CRDS-SCGIM were determined, and compared with those obtained using gas chromatography (GC) and isotope ratio mass spectrometry (IRMS), respectively. We examined the method regarding quantifying SR with various concentrations and enrichment of glucose and then applied it to investigate the responses of SR to the addition of different exogenous organic materials (glucose and rice residues) into paddy soils during a 21-day incubation. RESULTS: The CRDS-SCGIM CO2 and δ13C measurements were conducted with high precision (< 1.0 µmol/mol and 1‰, respectively). The optimal sampling interval and the amount added were not exceeded 4 h and 200 mg C/100 g dry soil in a 1 L incubation bottle, respectively; the 13C-enrichment of 3%-7% was appropriate. The total SR rates observed were 0.6-4.2 µL/h/g and the exogenous organic materials induced -49%-28% of priming effects in native SOM mineralisation. CONCLUSIONS: Our results show that CRDS-SCGIM is a method suitable for the quantification of soil microbial CO2 respiration, requiring less extensive lab resources than GC/IRMS.

Intensive N2 fixation accelerates microbial turnover in cropland soils.

Biological nitrogen fixation (BNF) is strongly affected by the carbon (C) and nitrogen (N) stoichiometry in soil and depends on the input of organic C. Due to the high metabolic costs of nitrogenase activity, however, the response of BNF to organic C input and its impact on microbial turnover remain unclear. To address this knowledge gap, we combined 15N2 tracing with high-throughput sequencing by adding glucose or glucose plus mineral N fertilizer for a 12-day incubation in three cropland soils. Glucose addition alone strongly changed the BNF activity (0.76-2.51 mg N kg-1 d-1), while BNF was completely absent after mineral N fertilization. This switch-on of BNF by glucose addition supported equally high rates of microbial growth and organic C mineralization compared with the direct mineral N assimilation by microorganisms. Glucose-induced BNF was predominantly catalyzed by Azotobacter-affiliated free-living diazotrophs (>50 % of the total nifH genes), which increased with diverse nondiazotrophs such as Nitrososphaera, Bacillus and Pseudoxanthomonas. Structural equation models (SEMs) and random forest (RF) analyses consistently revealed that the soil C:N ratio and Azotobacter-affiliated diazotrophic abundances were the key factors affecting glucose-induced BNF. Our findings emphasize the importance of free-living diazotrophs for microbial turnover of organic C in soil.

Effects of microplastics on photosynthesized C allocation in a rice-soil system and its utilization by soil microbial groups.

The effect of microplastics (MPs) on the allocation of rice photosynthetic carbon (C) in paddy systems and its utilization by soil microorganisms remain unclear. In this study, 13C-CO2 pulse labeling was used to quantify the input and allocation of photosynthetic C in a rice-soil system under MPs amendment. Rice was pulse-labeled at tillering growth stage under 0.01% and 1% w/w polyethylene (PE) and polyvinyl chloride (PVC) MP amendments. Plants and soils were sampled 24 h after pulse labeling. Photosynthesized C in roots in MP treatments was 30-54% lower than that in no-MP treatments. The 13C in soil organic C (SOC) in PVC-MP-amended bulk soil was 4.3-4.7 times higher than that in no-MP treatments. PVC and high-dose PE increased the photosynthetic C in microbial biomass C in the rhizosphere soil. MPs altered the allocation of photosynthetic C to microbial phospholipid fatty acid (PLFA) groups. High-dose PVC increased the 13C gram-positive PLFAs. Low-dose PE and high-dose PVC enhanced 13C in fungal PLFAs in bulk soil (including arbuscular mycorrhizal fungi (AMF) and Zygomycota) by 175% and 197%, respectively. The results highlight that MPs alter plant C input and microbial utilization of rhizodeposits, thereby affecting the C cycle in paddy ecosystems.

Anaerobic primed CO2 and CH4 in paddy soil are driven by Fe reduction and stimulated by biochar.

Soil C inputs and its priming effect (PE) are important in regulating soil C accumulation and mitigating climate change; however, the factors that control the direction and intensity of PE remains unclear. Soil C accumulation is strongly affected by the reductive iron status in paddy fields, while the addition of organic substances increases the emission of certain gases (CO2/CH4) under the PE, contributing to climate change. Here, we elucidated the mechanism by which Fe reduction, measured by Fe(II) production, regulates PE for CO2 and CH4 in paddy soils. Specifically, we quantified PE induced by 13C-labeled straw in anaerobic paddy soil, augmented by ferrihydrite and/or biochar, over 150 days in a laboratory experiment. The PE of CO2 was initially negative (-15.3 to -41.5 mg C kg-1) before 20 days of incubation and subsequently became positive. PE intensity for both gases depended on ferrihydrite or biochar application. Straw+biochar had the highest PEs (CO2, 116.5 mg C kg-1; CH4, 309.4 mg C kg-1), while straw+ferrihydrite produced the lowest PEs (CO2, 41.3 mg C kg-1; CH4, 107.8 mg C kg-1). Fe reduction was approximately three times higher with straw+ferrihydrite than with straw alone and was further stimulated by additional biochar. Thus, biochar appeared to accelerate Fe reduction, destabilize mineral-bound organic C, and increase nutrient availability to microbes. Enhanced microbial C and N mining led to a positive PE for CO2. Cumulative PE for CH4 was 2-3 times higher than that for CO2, indicating conversion via methanogenesis. Biochar acted as an electron shuttle, increasing Fe reduction and stimulating interspecies electron transfer, and increased CH4 production. Therefore, Fe reduction and biochar jointly increased PE intensity for CH4. In conclusion, water and fertilizer management of paddy soil could contribute toward mitigating climate change.

Microplastics in soil can increase nutrient uptake by wheat.

Microplastics can perturb microbial nutrient-mining strategies. However, the mechanism by which microplastics affect the resource-acquisition strategies of crops in agricultural systems remains unknown. The nutrient-acquisition potential of crops and microbes was investigated under treatments with two common microplastics (polyethylene [PE] and polyvinyl chloride [PVC]) at 0%, 1%, and 5% (w/w). Different root resource-acquisition strategies disturbed microbial nutrient turnover in the rhizosphere in response to microplastic addition. Specifically, the ß-1,4-glucosidase (BG) hotspot expanded, whereas the rhizosphere expansion of BG activity decreased. A decrease of less than PE1% (w/w) and an expansion of less than PE5% (w/w) in the 1,4-N-acetyl-glucosaminidase (NAG) hotspot with wider rhizosphere expansion of NAG activity indicated that higher doses of PE allow roots to uptake additional N. The phosphomonoesterase (PHOS) hotspot decreased in PE1% (w/w) and expanded in PE5% (w/w), but rhizosphere expansion did not change under PE treatments. However, both NAG and PHOS hotspots expanded with decreasing rhizosphere expansion under PVC treatments, indicating that PVC limits the utilization of available N and P, forcing the crop to obtain nutrients from the narrow root zone. These results indicate that adding PE microplastics increases the demand for and consumption of NH4+-N and NO3--N by wheat.

[Effect of Long-term Straw Returning on the Mineralization and Priming Effect of Rice Root-carbon].

Long-term straw returning to the field changes the environmental conditions of rice paddy soil, which affects the mineralization and priming effect of residual rice roots in the soil, but the direction and intensity of its influence is not clear. Therefore, based on a long-term fertilization field experiment, 13C-CO2 isotopic labeling technology and laboratorial incubation were used to analyze the characteristics of mineralization of rice roots and native soil organic carbon, the intensity and direction of the priming effect, and the source partitioning of CO2 emissions in three treatments, consisting of no fertilization (CK), chemical fertilizer (CF), and straw returning with chemical fertilizer (CFS). The results showed that after 120 days of flooding incubation, the root residue (R) increased the cumulative CO2 emissions by 617.41-726.27 mg·kg-1. The cumulative CO2 emissions from roots and root mineralized proportions in the CFS+R and CF+R treatments were 470.82 and 444.04 mg·kg-1, respectively, and 18.8% and 17.8%, respectively. These were significantly higher than those in the CK+R treatment (384.19 mg·kg-1, 15.4%). There was no significant difference in the cumulative CO2 emissions from native soil organic carbon among the three treatments. However, the mineralized proportion of native soil organic carbon in the CFS+R treatment (4.2%) was significantly lower than that in the CF+R and CK+R treatments (5.4% and 5.8%). The priming effect in the CFS+R treatment was 29.6%, which was significantly lower than that in the CK+R treatment (42.5%) and higher than that in the CF+R treatment (14.4%). A total of 23.47% to 27.59% of the cumulative CO2 emission of the flooded paddy soil was from the roots, and the remainder was from the soil. In addition, the proportion of CO2 emission caused by the priming effect was smaller in the CFS+R treatment than that in the CK+R treatment and larger than that in the CF+R treatment. In summary, the long-term straw returning in the flooded paddy soil will increase the mineralization potential of rice roots, but it is more conducive to the stability of the native soil organic carbon.

Microplastics shape microbial communities affecting soil organic matter decomposition in paddy soil.

Microplastics (MPs) can alter microbial communities and carbon (C) cycling in agricultural soils. However, the mechanism by which MPs affect the decomposition of microbe-driven soil organic matter remains unknown. We investigated the bacterial community succession and temporal turnover during soil organic matter decomposition in MP-amended paddy soils (none, low [0.01% w/w], or high [1% w/w]). We observed that MPs reduced the CO2 efflux rate on day 3 and subsequently promoted it on day 15 of incubation. This increased CO2 emission in MP-amended soil may be related to (i) enhanced hydrolase enzyme activities or; (ii) shifts in the Shannon diversity, positive group interactions, and temporal turnover rates (from 0.018 to 0.040). CO2 efflux was positively correlated (r > 0.8, p < 0.01) with Ruminiclostridium_1, Mobilitalea, Eubacterium xylanophilum, Sporomusa, Anaerobacteriu, Papillibacter, Syntrophomonadaceae, and Ruminococcaceae_UCG_013 abundance in soil with high MPs, indicating that these genera play important roles in soil organic C mineralization. These results demonstrate how microorganisms adapt to MPs and thus influence the C cycle in MP-polluted paddy ecosystems.

Experimental evidence for the impact of phages on mineralization of soil-derived dissolved organic matter under different temperature regimes.

Microbial mineralization of dissolved organic matter (DOM) plays an important role in regulating C and nutrient cycling. Viruses are the most abundant biological agents on Earth, but their effect on the density and activity of soil microorganisms and, consequently, on mineralization of DOM under different temperatures remains poorly understood. To assess the impact of viruses on DOM mineralization, we added soil phage concentrate (active vs. inactive phage control) to four DOM extracts containing inoculated microbial communities and incubated them at 18 °C and 23 °C for 32 days. Infection with active phages generally decreased DOM mineralization at day one and showed accelerated DOM mineralization later (especially from day 5 to 15) compared to that with the inactivated phages. Overall, phage infection increased the microbially driven CO2 release. Notably, while higher temperature increased the total CO2 release, the cumulative CO2 release induced by phage infection (difference between active phages and inactivated control) was not affected. However, higher temperatures advanced the response time of the phages but shortening its active period. Our findings suggest that bacterial predation by phages can significantly affect soil DOM mineralization. Therefore, higher temperatures may accelerate host-phage interactions and thus, the duration of C recycling.

[Characteristics of Paddy Soil Organic Carbon Mineralization and Influencing Factors Under Different Water Conditions and Microbial Biomass Levels].

Paddy soil often undergoes frequent dry-wet alternation. The change in water status not only affects the physical and chemical properties of the soil, but also changes the structure and diversity of the soil microbial communities, which in turn determines the rate of soil organic carbon mineralization. However, the effects of different water conditions and soil microbial biomass levels on the process of soil organic carbon mineralization and its mechanisms are still unclear. Therefore, this study took typical subtropical paddy soil as the research object, applied a laboratory incubation experiment with two water treatments of dry-wet and continuous flooding, and reduced the soil microbial biomass through chloroform fumigation, thereby obtaining high and low soil microbial biomass carbon contents, to elucidate the influencing mechanisms of microbial biomass and water conditions on organic carbon mineralization in paddy soil. The results showed that during the first 30 d of incubation, the dry-wet treatment was in a non-flooded stage and its cumulative CO2 emissions were significantly lower than those of the continuous flooded treatment. After 30 d, the dry-wet treatment entered the flooded stage. The difference in the cumulative CO2 emissions of the soils with a high microbial biomass carbon content between the dry-wet and continuous flooding treatments gradually decreased, and there was no significant difference on day 78. In the soil with a low microbial biomass carbon content, the cumulative CO2 emissions of the dry-wet treatment on day 78 was still significantly lower than that of the continuous flooded treatment. The soils with a low microbial biomass carbon content showed a faster CO2 emission rate at the beginning of the incubation period (first 20 d), which was 1.1-6.1 times greater than that of the high microbial biomass carbon soils owing to their high soil dissolved organic carbon (DOC) content, and the CO2 emission rate then gradually decreased until it was below that of the soil with a high microbial biomass carbon content. The soil organic carbon mineralization rate became stable later in the incubation period (days 45-78). The stable mineralization rate of the high microbial biomass carbon soil was 20%-30% higher than that of the low microbial biomass carbon soil. The multiple regression analysis results showed that the decrease in the soil DOC content (ΔDOC) and the increase in the Fe2+ content (ΔFe2+) significantly affected the change in cumulative CO2 emissions (ΔCO2) under continuous flooding conditions, but had no effect on ΔCO2 during the flooding stage of the dry-wet treatment. The correlation analysis showed that the daily CO2 emission rate of soils with high microbial biomass carbon was significantly positively correlated with glucosidase activity under dry-wet treatment and significantly negatively correlated with acetylglucosaminidase (NAG) and peroxidase activities under continuous flooding treatment. In the low microbial biomass carbon soils, the daily CO2 emission rate of the continuous flooding treatment was negatively correlated with the NAG activity, but showed no correlation with enzyme activities under dry-wet management. In summary, the cumulative CO2 emissions of dry-wet treatment were lower than those of continuous flooding treatment, and the difference was significant in soils with low microbial biomass carbon. The size of the soil microbial biomass determined the level of the stable soil organic carbon mineralization rate. The amount of soluble organic carbon and iron reduction affected the soil CO2 emissions under continuous flooding conditions, and the soil water conditions affected the daily CO2 emission rate and its key influencing enzymes. This study provides data and theoretical support for the carbon cycle and carbon sequestration potential in paddy soil.

[Effect of Water Management on Rice Growth and Rhizosphere Priming Effect in Paddy Soils].

The rhizosphere priming effect (RPE) caused by carbon inputs from crop rhizodeposits plays a key role in regulating the carbon emission flux and carbon balance of farmland soils. Due to frequent alternations between dry and wet conditions, CO2 and CH4 emissions and the RPE in paddy field ecosystems are significantly different to those of other ecosystems. Therefore, it is of great significance to determine the direction and intensity of the rice RPE under alternations of dry and wet to limit greenhouse gas emissions. In this study, using a 13C-CO2 continuous labeling method combined with a pot-based experiment, the response of rice growth and the RPE under alternating dry and wet and continuous flooding conditions was examined. The results showed that, compared with the continuous flooding treatment, the alternating dry and wet treatments significantly increased aboveground and root biomass and the root-to-root ratio, and also increased soil microbial biomass. Under continuous flooding conditions, fluxes of 13CO2 and 13CH4 increased with rice growth from 10.2 µg·(kg·h)-1 and 2.8 µg·(kg·h)-1 (63 d) to 16.0 µg·(kg·h)-1 and 3.2 µg·(kg·h)-1 (75 d), respectively. During the 12-day drying process, the emissions of 13CO2 and 13CH4 derived from rhizosphere deposited C decreased by 57.5% and 88.1%. Under continuous flooding conditions, the RPE for CO2 and CH4 were positive and increased with the growth of rice. Under the alternating dry and wet treatment, after 12 days of drying, the RPE for CO2 and CH4 was reduced from 0.29 mg·(kg·h)-1 and 12.3 µg·(kg·h)-1 (63 d) to -0.39 mg·(kg·h)-1 and 0.07 µg·(kg·h)-1 (75 d). Thus, alternating wet and dry treatment can effectively promote rice growth and reduce the cumulative emissions of CH4. Therefore, adopting appropriate field water management is of great significance for increasing rice yields and mitigating greenhouse gas emissions.

Effects of different stoichiometric ratios on mineralisation of root exudates and its priming effect in paddy soil.

In paddy soil, the root exudates strongly influence the microbial activity and soil organic matter (SOM) mineralisation. However, the stoichiometric regulation of the mineralisation of root exudates and their priming effect on paddy soil remains unclear. Thus, we used manipulative laboratory incubations to measure the mineralisation of root exudates and the subsequent priming effect in paddy soil under different stoichiometric conditions. In this study, root exudates (simulated by 13C-labelled glucose, alanine, and oxalic acid) were added to the paddy soil along with four different amounts of N and P. The addition of simulated root exudates (SREs) enhanced the total CO2 and CH4 emissions. The mineralisation of SREs decreased by 20-45% after the addition of N and P when compared with exclusive SREs application. The addition of N and P inhibited the SREs-derived CH4 emissions when compared with SREs application alone. The mineralisation of soil organic matter (SOM) increased with SREs application, thereby generating a positive priming effect for CO2 and CH4 emissions. However, the priming effect for CO2 and CH4 emissions was reduced with increased amounts of N and P. Furthermore, the addition of SREs with increasing N and P significantly enhanced the microbial SREs-derived C-use efficiency. Structural equation models indicated that NH4+-N and Olsen P negatively influenced the priming effect, whereas the microbial biomass and enzyme stoichiometry positively influenced the priming effect. In conclusion, our data suggest that SREs combined with increasing amounts of N and P could meet microbial stoichiometric demands and regulate microbial activity, which finally inhibited the mineralisation of SREs-C and the priming effect on paddy soil and positively affected C sequestration.

[Response of Extracellular Enzyme Activities to Substrate Availability in Paddy Soil with Long-term Fertilizer Management].

The availability of carbon (C), nitrogen (N), and other substrates in soil determines the growth and metabolism of microorganisms and affects the activity of extracellular enzymes. To study the activities of ß-1,4-glucosidase (BG) and ß-1,4-N-acetylglucosaminidase (NAG) in response to C and N availability, samples that underwent four treatments-non-fertilization (CK), chemical fertilizer (NPK), combination of organic manure and chemical fertilizer (OM), and mixture of straw and chemical fertilizer (ST)-were collected from long-term fertilization paddy soil and incubated for 0, 4, 8, and 12 months to obtain soil with different C and N availability gradients. The results showed that the dissolved organic carbon(DOC) content of OM and ST treatment samples was 2-3 times higher than that of CK and NPK treatment samples. With the increase of DOC and ammonium (NH4+-N) contents, the activities of BG and NAG and the contents of microbial biomass C (MBC) and N (MBN) showed no increase during incubation within each treatment. Fertilization treatments, incubation time, and their interaction are crucial factors varying the contents of DOC, NH4+-N, MBC, and MBN among different fertilization treatments (P<0.01). There was a positive correlation between MBC/MBN and DOC/NH4+-N of OM treatment (P<0.05) and a negative relationship between ln(BG)/ln(NAG) and DOC/NH4+-N of ST treatment (P<0.01), indicating that the availability of substrates played a key role in the potential activity of extracellular enzymes in paddy soil, and the carbon-nitrogen ratio of microbial biomass was controlled by the C/N stoichiometry of substrates in soil. The results have a certain guiding significance for further study on the variation of extracellular enzyme activity in paddy soil, regulating the balance of carbon and nitrogen, and improving the fertility of paddy soil.

Poly[[tetra-aqua-bis[µ(4)-2,2'-(p-phenyl-ene-di-oxy)diacetato][µ(2)-2,2'-(p-phenyl-ene-di-oxy)diacetato]dierbium(III)] hexa-hydrate].

The asymmetric unit of the title compound, [Er(2)(C(10)H(8)O(6))(3)(H(2)O)(4)]·6H(2)O, comprises one Er(3+) ion, one and a half 2,2'-(p-phenyl-enedi-oxy)diacetate (hqda) ligands, two coordinated water mol-ecules and three uncoordinated water mol-ecules. The Er(3+) ion is nine-coordinated by seven O atoms from hqda ligands and two O atoms from water mol-ecules. In the title compound, there are two types of crystallographically independent ligands: one with an inversion center in the middle of the ligand is chelating on both ends of the ligand towards each one Er center; the other hqda ligands are bridging-chelating on one side, and bridging on the other end of the ligand. Two adjacent Er(3+) ions are thus chelated and bridged by -COO groups from hqda ligands in three coordination modes (briding-chelating, bridging and chelating). These building blocks are linked by OOC-CH(2)O-C(6)H(4)-OCH(2)-COO spacers, forming two-dimensional neutral layers. Adjacent layers are linked by O-H⋯O hydrogen-bonding inter-actions, forming a three-dimensional supermolecular network.

catena-Poly[diaqua-tris(µ(3)-biphenyl-2,2-dicarboxyl-ato)disamarium(III)].

The title compound, [Sm(2)(C(14)H(8)O(4))(3)(H(2)O)(2)](n), is composed of one-dimensional chains and is isostructural with previously reported compounds [Wang et al. (2003 ▶). Eur. J. Inorg. Chem. pp. 1355-1360]. The asymmetric unit contains two Sm atoms, each of which lies on a crystallographic twofold axis. Both crystallographically independent Sm atoms are coordinated by eight O atoms in a distorted dodeca-hedral arrangement. The polymeric chains run along [001]. Adjacent chains are connected through π-π inter-actions [centroid-centroid distance = 3.450 (2) Å], forming a two-dimensional supra-molecular network.

[Transformation and Distribution of Soil Organic Carbon and the Microbial Characteristics in Response to Different Exogenous Carbon Input Levels in Paddy Soil].

The turnover of soil organic carbon (SOC) and the activity of soil microbes can be influenced by exogenous carbon. However, microbial response characteristics of the transformation and distribution of available organic carbon under different levels remain unclear in paddy soils. 13C-labeled glucose was used as a typical available exogenous carbon to simulate indoor culture experiments added at different levels of soil microbial biomass carbon (MBC) (0×MBC, 0.5×MBC, 1×MBC, 3×MBC, and 5×MBC) to reveal the process of C-transformation and distribution. The characteristics of microbial response in the process of exogenous carbon turnover was also monitored. The 96-well microplate fluorescence analysis was adopted to determine the activities of cellobiose hydrolase (CBH) and ß-glucosidase (ß-Glu). The results showed that, in 2 d of incubation, the ratio of labeled glucose carbon to dissolved organic carbon (13C-DOC/DOC) or to SOC (13C-SOC/SOC) was positively correlated with the amount of glucose added. The incorporation of glucose C (13C) into MBC reached the highest value (18.96 mg·kg-1) at 3×MBC treatment but decreased thereafter. The 13C allocation rate was mainly positively correlated with MBC, Olsen-P, and DOC. At 60 d, 13C-DOC, 13C-MBC, and 13C-SOC decreased significantly to less than 0.02 mg·kg-1, 2 mg·kg-1, and 10 mg·kg-1 in soil, and it was positively correlated with the amount of glucose added. Compared with CK, CBH enzyme activity increased significantly after the addition of glucose, and for the 3×MBC treatment it was increased by 22.6 times, which was significantly higher than those of other treatments (P<0.05). However, ß-Glu enzyme activity increased only in the 3×MBC and 5×MBC treatments, wherein it decreased with increasing amounts of added glucose. NH4+-N, pH, ß-Glu, and CBH were the primary factors affecting the distribution rate of 13C. In conclusion, the conversion of exogenous carbon to SOC increased with increased amounts of added organic carbon. This changed the activity of soil enzymes; however, microbial utilization of exogenous carbon may have a saturation threshold. Within the saturation threshold, the conversion rate of organic matter was directly proportional to the amount of added organic matter. When the saturation threshold was exceeded, the conversion rate of organic matter decreased. Therefore, the appropriate addition of exogenous carbon is beneficial, as it can increase SOC in rice fields and improve the quality of the crop growth environment.