Soil microbial activity is affected by Roundup WeatherMax and pesticides applied to cotton (Gossypium hirsutum)

Adoption of glyphosate-based weed control systems has led to increased use of the herbicide with continued use of additional pesticides. Combinations of pesticides may affect soil microbial activity differently than pesticides applied alone. Research was conducted to evaluate the influence of glyphosate-based cotton pest management systems on soil microbial activity. Soil was treated with commercial formulations of trifluralin, aldicarb, and mefenoxam + pentachloronitrobenzene (PCNB) with or without glyphosate (applied as Roundup WeatherMax). The soil microbial activity was measured by quantifying C and N mineralization. Soil microbial biomass was determined using the chloroform fumigation-incubation method. Soils treated with glyphosate alone exhibited greater cumulative C mineralization 30 days after treatment than all other treatments, which were similar to the untreated control. The addition of Roundup WeatherMax reduced C mineralization in soils treated with fluometuron, aldicarb, or mefenoxam + PCNB formulations. These results indicate that glyphosate-based herbicides alter the soil microbial response to other pesticides.     

Changes in soil microbial community structure by Allonychiurus kimi (Collembola) and their interactive effects on glyphosate degradation

Collembolans have been known to be involved in various soil ecosystem functions. However, the role of Collembola in organic contaminant degradation has not been sufficiently elucidated to assess its contribution. In this study, varying densities of Allonychiurus kimi (Lee, 1973) (0, 10, and 30 individuals per 30 g of soil) were introduced into glyphosate-contaminated soils (74.1 mg glyphosate kg⁻¹ soil). This study investigated changes in the microbial community and the residual glyphosate concentration in soils over incubation time to elucidate the effects of A. kimi on the glyphosate degradation through its influence on the microbial community. Furthermore, the investigation was conducted in soils collected in May and September 2018 to assess the contribution of A. kimi to glyphosate degradation in soils with varying microbial compositions and biomass. Autoclaved soil was used as a control to minimize the influence of indigenous soil microorganisms on glyphosate degradation. We hypothesize that as the initial density of A. kimi increases, the effects of A. kimi on the soil microbial community become pronounced, altering the degradation kinetics of glyphosate in the soil. The composition and biomass of the soil microorganisms were quantified using the phospholipid fatty acid (PLFA) method. Our study determined that the presence of A. kimi altered the microbial community structure by increasing the bacterial and total microbial, but not fungal, biomass. After seven days of treatment, the bacterial and total microbial biomass in the treatment with A. kimi were >2.0-fold and 1.5-fold greater, respectively, compared to those in the treatments without A. kimi. Specifically, the concentration of PLFA 18:1ω7c, i15:0, and 16:1ω7c was positively correlated with A. kimi density. The residual glyphosate concentration decreased exponentially over time as A. kimi density increased. At the end of the experiment, the remaining portions (%) of glyphosate in the May soil samples were 26.3, 20.1, and 6.2, with A. kimi densities of 0, 10, and 30 per vessel, respectively, and the portions in the September soil samples were 13.4, 12.7, and 2.2, respectively. The DT₅₀s (time required for 50 % degradation) decreased significantly with increasing A. kimi density, ranging from 6.8 to 10.1 days at an A. kimi density of 30 to 12.9–19.4 days without A. kimi. However, in the autoclaved soil, a similar effect was not apparent (i.e., DT₅₀s ranged from 23.3 to 27.4 days). Our study demonstrated that Collembola can enhance organic contaminant degradation in soils by altering the microbial community structure.     

Response of Mycorrhizal Infection to Glyphosate Applications and P Fertilization in Glyphosate-Tolerant Soybean,Maize, and Cotton

Glyphosate and phosphorus (P) fertilizer may alter arbuscular mycorrhizal (AM) fungal infection rates of glyphosate-tolerant cotton, maize, and soybean in low-P soil. Microbial biomass, water soluble P, Mehlich-3 P, and acid and alkaline phosphatase activities were not significantly impacted by glyphosate or P in the greenhouse. Phosphorus fertilization decreased mycorrhizal infection rates in cotton and maize and increased shoot biomass and shoot P in soybean in 2005, and decreased mycorrhizal infection in soybean and increased shoot biomass in cotton and maize and shoot P in all three crops in 2006. In pasteurized soil, glyphosate decreased percent mycorrhizal infection in maize, increased infection in cotton, and did not significantly affect infection in soybean. When soil was not pasteurized, glyphosate did not significantly alter mycorrhizal infection in any crop. The potential for glyphosate to alter AM fungal infection in glyphosate-tolerant plants may depend on whether soil microbial communities are compromised by other factors.     

Changes in microbial community structure following herbicide (glyphosate) additions to forest soils

Glyphosate applied at the recommended field rate to a clay loam and a sandy loam forest soil resulted in few changes in microbial community structure. Total and culturable bacteria, fungal hyphal length, bacterial:fungal biomass, carbon utilization profiles (BIOLOG), and bacterial and fungal phospholipid fatty acids (PLFA) were unaffected 1, 3, 7, or 30 days after application of a commercial formulation (Roundup^®). In contrast, a high concentration of glyphosate (100× field rate) simulating an undiluted chemical spill substantially altered the bacterial community in both soils. Increases in total bacteria, culturable bacteria, and bacterial:fungal biomass were rapid following application. Culturable bacteria increased from about 1% of the total population in untreated soil to as much as 25% at the high concentration by day 7, indicating enrichment of generalist bacteria. Community composition in both soils shifted from fungal dominance to an equal ratio of bacteria to fungi. Functional diversity of culturable bacteria, estimated by C substrate utilization, also increased at the high glyphosate concentration, particularly in the clay loam soil. Unlike the other bacterial indices, only minor changes in bacterial PLFA resulted after the third day following the 100× field rate application. Apparently the herbicide resulted in an across-the-board stimulation of bacteria that was not reflected by the finer-scale PLFA community structure. Changes in fungal properties (hyphae, propagules, PLFA biomarkers) were few and transient. We conclude that the commercial formulation of glyphosate has a benign affect on community structure when applied at the recommended field rate, and produces a non-specific, short-term stimulation of bacteria at a high concentration.     

乙草胺、甲胺磷及其复合污染对黑土土壤真菌的影响

Using plate counting and ergosterol assay, single and joint effects of acetochlor and methamidophos on the dynamics of soil fungal population and total fungal biomass in the black soil zone of Northeast China were investigated. The results demonstrated that acetochlor at high concentration levels （150 and 250 mg kg^-1） had an acute and mostly chronic toxicity on both the soil fungal population and total fungal biomass, but at a low concentration （50 mg kg^-1） generally had a stimulating effect that was stronger with total fungal biomass than with the soil fungal population. Methamidophos at a high concentration level （250 mg kg^-1） alone and almost all of its combinations with various dosages of acetochlor increased the soil fungal population, whereas at most sampling dates with 250 mg methamidophos kg^-1 soil, total fungal biomass increased, but in combination with acetochlor it was decreased in the early period of incubation and then increased 28 days after incubation. Thus, through measuring the number of colony forming unit of the soil fungal population along with the total fungal biomass, a better understanding on effects of agrochemicals on soil fungi could be made.     

Comparative sorption and leaching study of the herbicides fluometuron and 4-chloro-2-methylphenoxyacetic acid (MCPA) in a soil amended with biochars and other sorbents

Biochar, the solid residual remaining after the thermochemical transformation of biomass for carbon sequestration, has been proposed to be used as a soil amendment, because of its agronomic benefits. The effect of amending soil with six biochars made from different feedstocks on the sorption and leaching of fluometuron and 4-chloro-2-methylphenoxyacetic acid (MCPA) was compared to the effect of other sorbents: an activated carbon, a Ca-rich Arizona montmorillonite modified with hexadecyltrimethylammonium organic cation (SA-HDTMA), and an agricultural organic residue from olive oil production (OOW). Soil was amended at 2% (w/w), and studies were performed following a batch equilibration procedure. Sorption of both herbicides increased in all amended soils, but decreased in soil amended with a biochar produced from macadamia nut shells made with fast pyrolysis. Lower leaching of the herbicides was observed in the soils amended with the biochars with higher surface areas BC5 and BC6 and the organoclay (OCl). Despite the increase in herbicide sorption in soils amended with two hardwood biochars (BC1 and BC3) and OOW, leaching of fluometuron and MCPA was enhanced with the addition of these amendments as compared to the unamended soil. The increased leaching is due to some amendments' soluble organic compounds, which compete or associate with herbicide molecules, enhancing their soil mobility. Thus, the results indicate that not all biochar amendments will increase sorption and decrease leaching of fluometuron and MCPA. Furthermore, the amount and composition of the organic carbon (OC) content of the amendment, especially the soluble part (DOC), can play an important role in the sorption and leaching of these herbicides.     

Nutrient Seepage from Operating Turkey Buildings with a Litter System

The effect of selected nutrient amendments and temperature on the biodegradation of pentachlorophenol (PCP) within a soil biopile was studied on a laboratory scale. This was accomplished by monitoring microbial populations, the concentration of PCP and the release of inorganic chloride ions in the contaminated soil. It was found that temperatures of 10, 15 and 20 °C had no significant effect on microbial populations and the percentage of PCP remaining in the soil. However, the nutrient amendments did have a significant effect on the parameters measured. The dairy manure, ammonium nitrate fertilizer and control treatments all experienced some fluctuations in the amount of PCP remaining in the soil over the incubation period and may have been due to the release of initially unextractable bound residues. PCP decreased by 76% in the municipal solid waste compost amended soil, while the concentration of inorganic chloride ions increased. The municipal solid waste compost treatment had significantly higher bacterial and fungal populations. Based on the results of this study municipal solid waste compost may be used as an effective supplemental nutrient amendment for the degradation of PCP in soil biopiles.     

Does soil ergosterol concentration provide a reliable estimate of soil fungal biomass?

Our aim was to determine if soil ergosterol concentration provides a quantitative estimate of the soil fungal biomass concentration, as is usually assumed. This was done by comparing soil ergosterol measurements with soil fungal biomass (fungal biomass C) concentrations estimated by microscopic measurements and by the selective inhibition technique linked to substrate-induced respiration (SIR). The measurements were compared in a silty-clay loam soil given a range of previous treatments designed to increase or decrease the soil fungal biomass and so also to change the soil ergosterol concentration. The treatments used were ryegrass amendment, to increase the total and fungal biomass, and CHCl₃-fumigation and the addition of the biocides, captan, bronopol and dinoseb, to decrease both ergosterol and fungal biomass C concentrations. The mineralization of ergosterol following addition to sand innoculated with soil extract, and to a sandy loam soil, was also determined. The added ergosterol was little, if at all, degraded following addition to either sand or the unfumigated or fumigated soil during a 10 d aerobic incubation. Similarly, pesticide addition did not significantly change soil ergosterol concentrations yet the soil fungal biomass C concentration decreased significantly. Thus, the ratio: (soil ergosterol concentration/soil fungal biomass C concentration) was much higher in the pesticide-treated soils than the control soil. Following ryegrass amendment, soil ergosterol concentration increased from about 6-12 μg⁻¹ soil within 5 d and then decreased gradually to about 7 μg g⁻¹ soil by 20 d incubation. Changes in fungal biomass C (measured by direct microscopy) closely mirrored changes in soil ergosterol over this period. However, when the amended soil was fumigated and then incubated for a further 5 d, the initial ergosterol concentration declined from 7 to 5 μg g⁻¹ soil by 20 d incubation (a decline of about 0.4). The comparable decline in fungal biomass C was about eight-fold. Thus the ratio of ergosterol to fungal biomass C increased from 0.005 to about 0.01. There was a significant correlation (r>0.84, P<0.001) between soil ergosterol concentration and fungal biomass measured by either SIR or microscopy. However, three data points played a vital role in the correlation. When these points were excluded the relationship was very poor (r<0.4). Our results therefore suggest that substantial amounts of ergosterol may exist, other than in living cells, for considerable periods, with little, if any mineralization. Thus, these results indicate that ergosterol and fungal biomass C concentrations are not always closely correlated, due to the slow metabolism of ergosterol in recently dead fugal biomass and/or the existence of exocellular ergosterol in soil.     

Influence of incubation temperature on the behavior of triethylamine-extractable glyphosate (N-phosphonomethylglycine) in four soils

The behavior of glyphosate, extracted from four soils using aqueous triethylamine, was investigated at two temperatures. For each soil, and at both temperatures, there was a marked loss in the amount of extractable glyphosate immediately after addition of the herbicide to soil. This rapid loss of glyphosate was ascribed to adsorption of the herbicide into a nonextractable form. For three of the four soils used when incubated at 25 degrees C, the rates of loss of extractable glyphosate were similar to previously measured rates of degradation of this herbicide in these soils. However, loss of extractable glyphosate from the Culgoa clay loam was due not only to substrate degradation but also to slow sorption of glyphosate into the nonextractable form in this soil over the experimental period. For the Rutherglen and Walpeup soils, when incubated at 10 degrees C, the rates of loss of extractable glyphosate were half of the previously measured rate of degradation of this herbicide in these soils. However, there was no measured loss of extractable glyphosate from the Wimmera clay. As previous work has shown glyphosate to decompose readily in these soils at this temperature, these findings suggest that desorption of glyphosate may occur at a rate greater than degradation at this temperature and, hence, that temperature may play a pivotal role in sorption processes. Investigations with these soils when sterilized by gamma-irradiation showed that for the Walpeup, Wimmera, and Rutherglen soils, sorption was complete soon after the addition of the herbicide; however, for the Culgoa soil, further adsorption occurred over the entire experimental period.     

Reponse de la biomasse microbienne a l'adjonction au sol de materiel vegetal marque au 14C: Role des racines vivantes

¹⁴C and ¹⁵N-labelled immature wheat straw was incubated in the laboratory for 450 days in either a sandy soil or a clay soil, under controlled conditions of temperature and humidity. One-half of the treatments were cropped 4 times in succession with spring wheat. After each harvest, the roots and shoots were removed from the soil. The remaining treatments were kept bare, without plants. After 277 days, 1% unlabelled wheat straw was again mixed with the soils. Microbial biomass was measured after 0, 25, 53, 80, 185, 318 and 430 days, using the fumigation technique. This paper presents the ¹⁴C-data.The half-life of the labelled compounds in soil was from 60 to 70 days. After 430 days about 10% more labelled C remained in bare soil than in cropped soil. Labelled biomass carbon reached its maximum before day 25. By then 50% of the biomass-C was labelled and the biomass represented 20% of the total labelled C remaining in the soils. This percentage decreased slowly to 15% after 430 days in bare sandy soil and to 17% in bare clay soil. A second incorporation of plant material, this time unlabelled, did not appreciably alter the shape of the curve representing the decrease of labelled C in biomass, expressed as % of the total remaining labelled C. Total biomass-C (labelled + unlabelled) in cropped soil was sometimes higher and sometimes lower than in bare soil. However, the labelled C/total C ratio in biomass was always lower; in cropped soils than in soils without plants, clearly showing the effect of rhizodeposition. From days 25 to 430 an increasing difference appeared between the ratio labelled C/total and C in CO₂ and the corresponding ratio labelled C/total C in biomass. In CO₂-C the ratio diminished rapidly, in biomass-C it remained at a high level, most probably indicating a lower turnover of C in resting but living microorganisms. Other explanations are also discussed. The amount of CO₂-C released mg^?1 of biomass-C was higher in cropped than in bare soil, presumably because the microorganisms were activated by the living (or dying) root system.     

Turnover of microbial tissue in soil under field conditions

The microbial population of a Brown Chernozemic soil was labelled in situ by adding ¹⁴C-glucose and ¹⁵NH₄¹⁵NO₃ to the plow layer. The loss of ¹⁴C, nitrogen immobilization-mineralization reactions, bacterial numbers (plate count, direct count) and fungal hyphal lengths were determined periodically throughout the growing period in amended and unamended microplots and in the surrounding field soil. After 5 days, 90 per cent of the labelled N occurred in the organic form with little subsequent mineralization. Of the labelled C added, 63, 56 and 39 per cent, remained in the soil after 3, 14 and 104 days, respectively.The ratio of fungal C to bacterial C increased as soil moisture decreased. Viable (plate count) and total numbers of bacteria in samples from unamended plots and field soil were significantly correlated with each other and with soil moisture. Fungal hyphal lengths from amended soil were also significantly related to moisture but the rate of loss of ¹⁴C and mineralization of ¹⁵N were not. The synthesized microbial material (tissue and metabolites) exhibited a high degree of stability throughout the study. The half-life of labelled C remaining in the soil after 30 days was calculated to be 6 months compared to only 4 days for the added glucose C. The amount of energy used for maintenance by the soil population under field conditions was calculated from measurements of biomass C, respired labelled C and respired soil C.     

Factors affecting N immobilisation/mineralisation kinetics for cellulose-, glucose- and straw-amended sandy soils

The kinetics of N immobilisation/mineralisation for cellulose-, glucose- and straw-amended sandy soils were investigated in a series of laboratory incubations. Three Scottish soils expected to exhibit a range of biological activity were used: a loamy sand, intensively cropped horticultural soil subject to large inputs of inorganic fertilisers and pesticides (Balmalcolm - pH 7.2, organic matter 3.3%); a sandy loam soil highly enriched with organic manures and used for organic vegetable production (Strathmiglo - pH 7.1, organic matter 7.3%); and a loamy sand soil of low fertility in a zero-grazing, low intensity organic ley-arable rotation (Aldrochty pH 6.0, organic matter 5.0%). Incubations of soils with 1,000 mg cellulose-C kg^-1 soil at 8°C, showed peak N immobilisation of 71Lj, 92Lj and 65ᆣ mg N g^-1 added C for the Balmalcolm (after 34 days), Strathmiglo (after 34 days) and Aldrochty soils (after 63 days). The N remineralisation by the end of the incubation (>300 days) was 0, 50 and 22 mg N g^-1 cellulose-C in the Balmalcolm, Strathmiglo soil and Aldrochty soils, respectively. Only about 30% of the N immobilisation could be explained by soil microbial biomass N accumulation (much less than expected from model simulations). The C/N ratio of the extra microbial biomass was quite wide (19). Bacterial, protozoan and nematode biomass accounted for only 18%, 0.1% and 0.5% of the extra C immobilisation, respectively. These data suggest that fungal biomass growth and deposition of recalcitrant fungal metabolites are the main sinks for the N immobilised. With 1,000 mg glucose-C kg ^-1 added to the Balmalcolm soil, about 75 mg N g^-1 added C were immobilised after 6 days. Under less well aerated conditions at 15°C, immobilisation of only 10-20 mg N g^-1 added cellulose C took place in 2-4 weeks, but soluble organic C increased greatly. The N remineralised after 4-6 weeks.     

Mineralization of bacteria and fungi in chloroform-fumigated soils

It has been suggested by others that the size of the flush of mineralization caused by CHC1₃ fumigation can be used to estimate the amount of microbial biomass in soils. Calculation of biomass from the flush requires that the proportion of CHCl₃-killed cell C mineralized be known. To determine this proportion, 15 species of [¹⁴C]labelled fungi and 12 species of [¹⁴C]labelled bacteria were added to four types of soil and these were fumigated for 24 h with CHC1₃, reinoculated with unfumigated soil, and incubated at 22°C for 10 days. The average percentage mineralization of the fungi was 43.7 ± 5.3, while the average for the bacteria was 33.3 ± 9.9. Using a 1:3 ratio for distribution of total biomass between the bacterial and fungal populations, respectively, it was calculated that the average mineralization of both types of cells was 41.1%. In experiments conducted to determine if CHC1₃ vapour alters stabilized microbial metabolites or dead microbial cells in a manner which makes them more susceptible to degradation, it was found that both fumigated and unfumigated dead fungal materials mineralized to the same extent in soil during 10 days of incubation.     

Effect of Biochar Amendment and Ageing on Adsorption and Degradation of Two Herbicides

Biochar amendment can alter soil properties, for instance, the ability to adsorb and degrade different chemicals. However, ageing of the biochar, due to processes occurring in the soil over time, can influence such biochar-mediated effects. This study examined how biochar affected adsorption and degradation of two herbicides, glyphosate (N-(phosphonomethyl)-glycine) and diuron (3-(3,4-dichlorophenyl)-1,1-dimethylurea) in soil and how these effects were modulated by ageing of the biochar. One sandy and one clayey soil that had been freshly amended with a wood-based biochar (0, 1, 10, 20 and 30% w/w) were studied. An ageing experiment, in which the soil-biochar mixtures were aged for 3.5 months in the laboratory, was also performed. Adsorption and degradation were studied in these soil and soil-biochar mixtures, and compared to results from a soil historically enriched with charcoal. Biochar amendment increased the pH in both soils and increased the water-holding capacity of the sandy soil. Adsorption of diuron was enhanced by biochar amendment in both soils, while glyphosate adsorption was decreased in the sandy soil. Ageing of soil-biochar mixtures decreased adsorption of both herbicides in comparison with freshly biochar-amended soil. Herbicide degradation rates were not consistently affected by biochar amendment or ageing in any of the soils. However, glyphosate half-lives correlated with the Freundlich Kf values in the clayey soil, indicating that degradation was limited by availability there.     

Impact of cycloheximide addition on adenylates in soil

Cycloheximide inhibits specifically the ribosomal protein synthesis of eukaryotic cells, i.e. the metabolism of soil fungi. We measured cycloheximide effects on adenylates in 20 different soils (0-10 cm depth) from arable, grass and forest land with a large variety of soil properties. The aims were (1) to assess the interactions between cycloheximide effects and soil properties and (2) to prove the relationship between cycloheximide effects on ATP and the ergosterol-to-microbial biomass C ratio, which is an indicator for the fungal proportion of the total microbial biomass. The adenylates ATP, ADP and AMP were measured 6 h after adding either 10 mg cycloheximide per gram soil in combination with 24 mg talcum per gram soil or 24 mg talcum per gram soil solely. The medians of the relative increases in AMP and ADP were 45 and 25% and the medians of the relative decreases in ATP and adenylates were −36 and −12%. These changes in adenylate composition lead to a cycloheximide-induced relative decrease in the adenylate energy charge level of 15%. The relative decrease in ATP content after cycloheximide addition was significantly correlated with the ATP-to-microbial biomass C ratio, but not with the ergosterol-to-microbial biomass C ratio. The absolute increase in ADP and the absolute decrease in ATP were affected by the clay content according to principal component analysis. The reduction of the ATP-to-microbial biomass C ratio indicates that this ratio had the potential of being an important ecotoxicological indicator of direct toxic effects of organic pollutants on soil microorganisms.     

Microbial activity,community structure and potassium dynamics in rhizosphere soil of soybean plants treated with glyphosate

With the advent of glyphosate [N-(phosphonomethyl)glycine] tolerant crops, soils have now been receiving repeated applications of the herbicide for over 10 years in the Midwestern USA. There is evidence that long-term use of glyphosate can cause micronutrient deficiency but little is known about plant potassium (K) uptake interactions with glyphosate. The repeated use of glyphosate may create a selection pressure in soil microbial communities that could affect soil K dynamics and ultimately K availability for crops. Therefore, the objectives of this study were to characterize the effect of foliar glyphosate applied to GR (glyphosate resistant) soybeans on: (1) rhizosphere microbial community profiles using ester linked fatty acid methyl ester (EL-FAME) biomarkers, (2) exchangeable, non-exchangeable, and microbial K in the rhizosphere soil, and (3) concentrations of soybean leaf K. A greenhouse study was conducted in a 2 × 2 × 3 factorial design with two soil treatments (with or without long-term field applications of glyphosate), two plant treatments (presence and absence of soybean plants), and three rates of glyphosate treatments (0×, 1× at 0.87, and 2× at 1.74 kg ae ha^?1, the recommended field rate). After each glyphosate application, rhizosphere soils were sampled and analyzed for microbial community structure using ester linked fatty acid methyl ester biomarkers (EL-FAME), and exchangeable, plant tissue and microbial biomass K. Glyphosate application caused a significant decrease in the total microbial biomass in soybean rhizosphere soil that had no previous exposure to glyphosate, at 7 days after glyphosate application. However, no significant changes were observed in the overall microbial community structure. In conclusion, the glyphosate application lowered the total microbial biomass in the GR soybean rhizosphere soil that had no previous exposure to glyphosate, at 7 days after glyphosate application; caused no changes in the microbial community structure; and did not reduce the plant available K (soil exchangeable or plant tissue K).     

The effect of glyphosate on soil microbial activity,microbial community structure,and soil potassium

The herbicide, glyphosate [N-(phosphonomethyl) glycine] is extensively used worldwide. Long-term use of glyphosate can cause micronutrient deficiency but little is known about potassium (K) interactions with glyphosate. The repeated use of glyphosate may create a selection pressure in soil microbial communities that could affect the nutrient dynamics such as K. The objective of this study was to determine the effect of single or repeated glyphosate applications on microbial and K properties of soils. A 54 day incubation study (Exp I) had a 3 × 5 factorial design with 3 soils (silt loam: fine, illitic, mesic Aeric Epiaqualf) of similar physical and chemical characteristics, that varied in long-term glyphosate applications (no, low, and high glyphosate field treatments) and five glyphosate rates (0, 0.5×, 1×, 2×, and 3× recommended field rates applied once at time zero). A second 6 month incubation study (Exp II) had a 3 × 3 factorial design with three soils (as described above) and three rates of glyphosate (0, 1×, and 2× recommended field application rates applied monthly). For each study microbial properties [respiration; community structure measured by ester linked fatty acid methyl ester (EL-FAME) analysis and microbial biomass K] and K fractions (exchangeable and non-exchangeable) were measured periodically. For Exp I, glyphosate significantly increased microbial respiration that was closely related to glyphosate application rate, most notably in soils with a history of receiving glyphosate. For Exp II, there was no significant effect of repeated glyphosate application on soil microbial structure (EL-FAME) or biomass K. We conclude that glyphosate: (1) stimulates microbial respiration particularly on soils with a history of glyphosate application; (2) has no significant effect on functional diversity (EL-FAME) or microbial biomass K; and (3) does not reduce the exchangeable K (putatively available to plants) or affect non-exchangeable K. The respiration response in soils with a long-term glyphosate response would suggest there was a shift in the microbial community that could readily degrade glyphosate but this shift was not detected by EL-FAME.     

Glyphosate degradation as a soil health indicator for heavy metal polluted soils

Glyphosate is a commonly used herbicide in grassland soils and microorganisms control its degradation. We introduce the concept of using the degradation rate as an indicator for ecosystem health. Testing this concept, we used soils with a long history of heavy metal pollution (Cu, Pb, and Zn). We hypothesized lower degradation rates in metal-polluted compared to less polluted soils. The degradation rates were measured by repeated measurements of the parent compound in spiked soil-water slurries incubated at 20 °C over 21 days. Average rates showed no differences comparing among soils. We observed a positive correlation between glyphosate degradation rates and soil metal pollution. Therefore, we concluded that the expected impact of the metals on the bacteria responsible for the herbicide degradation was not established. We discuss the potential influence on biological degradation rates of soil pH and adsorption and implications using the concept of the soil health indicator.     

Effects of soil storage on the microbial community and degradation of metsulfuron-methyl

The effect storage had on the microbial biomass in two soils (Trevino and Fargo) was compared to the effect storage had on each soil's capacity to degrade metsulfuron-methyl. Soils were collected from the field and used fresh (<3 weeks old) or stored at 20 and 4 degrees C for 3 or 6 months. The phospholipid fatty acid content of the soils was used to monitor changes in the microbial biomass during storage and incubation in a flow-through apparatus. In both soils, [phenyl-U-14C]metsulfuron-methyl was used to monitor changes in the route and rate of degradation along with 14CO2 evolution (mineralization). Total microbial biomasses in both soils were significantly reduced for soils incubated in the flow-through apparatus, whereas only the Trevino soil's microbial biomass was significantly reduced as a result of storage. The microbial communities of both soils were significantly different as a result of storage as shown by discriminant analysis. In both soils, degradation rate, pathway of degradation, and mineralization of metsulfuron-methyl were significantly affected by storage compared to fresh soil. The half-life of metsulfuron-methyl increased significantly (P < 0.05) in the Trevino soil from 45 days (fresh) to 63 days (stored soil), whereas in the Fargo soil half-lives increased significantly (P < 0.05) from 23 days (fresh) to 29 days (soils stored for 6 months). In both soils, mineralization of [14C]metsulfuron-methyl was significantly (P < 0.05) higher in fresh soils compared to stored soils. The degradation pathways of metsulfuron-methyl changed with storage as evidenced by the loss of formation of one biologically derived metabolite (degradate) in stored soils compared to fresh soils.     

Tillage and cover effects on soil microbial properties and fluometuron degradation

This research concerns the influence of no tillage (NT) or conventional tillage (CT) and a ryegrass (Lolium multiforum Lam.) cover crop in a cotton (Gossypium hirsutum L.) production system on soil and ryegrass microbial counts, enzyme activities, and fluometuron degradation. Fluorescein diacetate hydrolysis, aryl acylamidase, and colony-forming units (CFUs) of total bacteria and fungi, gram-negative bacteria, and fluorescent pseudomonads were determined in soil and ryegrass samples used in the degradation study. Fluometuron (14C-labelled herbicide) degradation was evaluated in the laboratory using soil and ryegrass. The CT and NT plots with a ryegrass cover crop maintained greater microbial populations in the upper 2 cm compared to their respective no-cover soils, and CT soils with ryegrass maintained greater bacterial and fungal CFUs in the 2–10 cm depth compared to the other soils The highest enzymatic activity was found in the 0–2 cm depth of soils with ryegrass compared to their respective soils without ryegrass. Ryegrass residues under NT maintained several hundred-fold greater CFUs than the respective underlying surface soils. Fluometuron degradation in soil and ryegrass residues proceeded through sequential demethylation and incorporation of residues into nonextractable components. The most rapid degradation was observed in surface (0 to 2 cm) soil from CT and NT–ryegrass plots. However, degradation occurred more rapidly in CT compared to NT soils in the 2 to 10 cm depth. Ryegrass cover crop systems, under NT or incorporated under CT, stimulated microbiological soil properties and promoted herbicide degradation in surface soils.