Inhibition of mineralization of urea nitrogen in soil

Summary The effects of anthraquinones and some other quinonoid and phenolic compounds on mineralization of urea N in soils were studied by estimating the influence on urease activity and nitrification. Anthraquinones did not affect the mineralization of urea N but 1,4-naphthoquinone; 2-methyl-1,4-naphthoquinone; 2–3-dichlorohydroquinone; 4,6-di-tert.butyl-o-benzoquinone; 4-tert.butylpyrocatechol and 4,6-di-tert.butylpyrocatechol inhibited urease activity and nitrification. The hydrolysis of urea (100 ppm) was not prevented by partial reduction in urease activity. The effective substances also inhibited dehydrogenase activity.     

Nitrification and ammonia volatilisation losses from urea and dicyandiamide-treated urea in a sandy loam soil

Summary Nitrification and ammonia volatilisation losses from urea and dicyandiamide (DCD)-treated urea were studied in a sandy loam soil. Laboratory experiments indicated that 20 ppm (of soil) DCD effectively inhibited nitrification of urea over sixty days. If the urea was treated with DCD (20 ppm), ammonia emission from the soil was extended over 105 days; with urea alone, it was negligible after 15 days. A field study indicated that DCD treatment increased volatilisation losses of ammonia tremondously if urea was applied to the soil surface; these losses were minimised if the urea was placed at 5 cm depth. It would seem that nitrification inhibitors must be combined with a placement technique.     

Influence of Urea,Hydroxyurea, and Thiourea on Meloidogyne javanica and Infected Excised Tomato Roots in Culture

Urea (U), hydroxyurea (HU), and thiourea (TU), in various concentrations, were added to chemically defined plant tissue culture medium on which Meloidogyne javanica was reared on excised tomato roots. Concentrations as low as 3 ppm HU or 12 ppm TU inhibited nematode maturation by 70-90% 4 weeks after inoculation, and the coenocytes in the parasitized tissue were poorly developed. Gall weight was also inhibited by 50% in cultures treated with 3 and 6 ppm HU. However, exposing juveniles of M. javanica and Tylenchulus semipenetrans or juveniles and adults of Pratylenchus thornei to increasing concentrations of HU or TU, up to 100 ppm, was not lethal. These two urea derivatives still inhibited nematode maturation when the infected region of the root was not in direct contact with the chemicals. Therefore, we suggest that these urea derivatives inhibit nematode development by affecting the plant metabolism essential to coenocyte formation, an occurrence similar to the hypersensitive reaction in a naturally resistant plant.     

Studies on the persistence and effects on soil fauna of some soil-applied systemic insecticides

Granular formulations of menazon, phorate and thionazin were applied to a sandy loam soil (pH = 6·1)in April and May as in-row treatments at commercial rates. They were also broadcast and mixed into the top 4 in of soil at concentrations (10 and 250 ppm of dry soil) which simulated the local in-row concentrations in areas large enough for sampling. Bioassays showed that 50 % of phorate, thionazin and menazon equivalents had disappeared in about 68, 57 and 23 days respectively from soil treated with 10 ppm of the insecticides. Small residues of the 250 ppm treatments still remained 2 years later. The initial rate of loss of activity of thionazin applied at 250 ppm was much slower than from a 10 ppm application whereas the activities of 250 and 10 ppm of menazon disappeared at similar rates. Phorate at 250 ppm killed almost all earthworms, Collembola, Acarina, free-living saprophytic and parasitic nematodes and Protozoa; 10 ppm phorate and 250 ppm of menazon also killed almost all Collembola and Acarina but the menazon was relatively harmless to earthworms. Collembola and mite populations began to increase when residues of phorate and menazon equivalents had decreased to about 2 and 20 ppm respectively, and after 15 months they were similar to those in untreated plots. The broadcast treatments initially decreased the rate of breakdown of leaf discs put in the soil but, after about 4 weeks, breakdown increased, sometimes above that in untreated plots. This was associated with a large increase in numbers of Enchytraeidae which were apparently unaffected by the insecticides. Four months after application, 1 lb/acre of phorate and 2 lb of menazon applied in seed drills 2 ft apart were not affecting Collembola in soil between the rows but were still decreasing the numbers within them. In -row phorate distributed along a 1·5 in diameter band of soil, 3 in deep, killed Collembola 3 in on either side but not 6 in away. It did not spread upwards in toxic quantities, but after rainfall, sufficient to kill Collembola leached at least 3 in downwards. We conclude that commercial in-row applications of chemicals like phorate are most unlikely to harm soil fertility, especially as the leaf-litter-destroying function of Collembola and other animals killed by phorate may be taken over by Enchytraeidae.     

Valuation of efficacy and nonrepellency of indoxacarb and fipronil-treated soil at various concentrations and thicknesses against two subterranean termites (Isoptera: Rhinotermitidae)

The efficacy and nonrepellency of indoxacarb (150 SC, 150 g [AI]/liter) and fipronil (Termidor SC, 9.1% [Al]) against field-collected eastern subterranean termite, Reticulitermes flavipes (Kollar), and the Formosan subterranean termite, Coptotermes formosanus Shiraki, were evaluated for mortality and penetration into treated soil in laboratory glass tube bioassays. Both insecticides were tested at five concentrations (0, 1, 10, 50, and 100 ppm) and two thicknesses (20 and 50 mm) of treated soil. Indoxacarb caused significantly greater mortality than controls at all treatment thicknesses of > or = 10 ppm, but not at 1 ppm. Concentration and treatment thickness of indoxacarb significantly affected termite mortality. Eastern subterranean termites were significantly more susceptible to indoxacarb than Formosan subterranean termites, but there were no intercolony differences in either species. Termites completely penetrated through all treatment thickness of indoxacarb-treated soil at all concentrations, except one of the six Formosan subterranean termite replicates of 50 mm at 50 ppm, when all termites were killed before tunneling through the treated soil. Fipronil resulted in significantly faster and greater termite mortality than indoxacarb at corresponding concentrations. Concentration and treatment thickness of fipronil also significantly affected termite mortality. There was no intercolony difference in susceptibility to either insecticide in either termite. Both termite species completely penetrated 20-mm treatments of all tested fipronil concentrations, as well as 50-mm soil treated with fipronil at < or = 10 ppm. At 50 and 100 ppm fipronil, termites tunneled only a mean of 87 +/- 0.21 and 47 +/- 0.18% deep into 50-mm treated soil, respectively, before death. Both insecticides demonstrated a delayed mode of activity and nonrepellency against the two termite species.     

Influence of 2,4,6-trinitrotoluene (TNT) concentration on the degradation of TNT in explosive-contaminated soils by the white rot fungus Phanerochaete chrysosporium.

The ability of Phanerochaete chrysosporium to bioremediate TNT (2,4,6-trinitrotoluene) in a soil containing 12,000 ppm of TNT and the explosives RDX (hexahydro-1,3,5-trinitro-1,3,5- triazine; 3,000 ppm) and HMX (octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine; 300 ppm) was investigated. The fungus did not grow in malt extract broth containing more than 0.02% (wt/vol; 24 ppm of TNT) soil. Pure TNT or explosives extracted from the soil were degraded by P. chrysosporium spore-inoculated cultures at TNT concentrations of up to 20 ppm. Mycelium-inoculated cultures degraded 100 ppm of TNT, but further growth was inhibited above 20 ppm. In malt extract broth, spore-inoculated cultures mineralized 10% of added [14C]TNT (5 ppm) in 27 days at 37 degrees C. No mineralization occurred during [14C]TNT biotransformation by mycelium-inoculated cultures, although the TNT was transformed.     

Influence of 2,4,6-trinitrotoluene (TNT) concentration on the degradation of TNT in explosive-contaminated soils by the white rot fungus Phanerochaete chrysosporium.

The ability of Phanerochaete chrysosporium to bioremediate TNT (2,4,6-trinitrotoluene) in a soil containing 12,000 ppm of TNT and the explosives RDX (hexahydro-1,3,5-trinitro-1,3,5- triazine; 3,000 ppm) and HMX (octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine; 300 ppm) was investigated. The fungus did not grow in malt extract broth containing more than 0.02% (wt/vol; 24 ppm of TNT) soil. Pure TNT or explosives extracted from the soil were degraded by P. chrysosporium spore-inoculated cultures at TNT concentrations of up to 20 ppm. Mycelium-inoculated cultures degraded 100 ppm of TNT, but further growth was inhibited above 20 ppm. In malt extract broth, spore-inoculated cultures mineralized 10% of added [14C]TNT (5 ppm) in 27 days at 37 degrees C. No mineralization occurred during [14C]TNT biotransformation by mycelium-inoculated cultures, although the TNT was transformed.     

The effect of the systemic fungicide benomyl on survival and reproduction of the bird cherry aphid (Rhopalosiphum padi)

Weight gain and intrinsic rate of population increase (r_m) of Rhopalosiphum padi were measured on wheat plants given soil drenches of benomyl at various concentrations. Reduced weight gain occurred with concentrations as low as 3.125 ppm. Mortality of aphids significantly exceeded control mortality at 25 ppm, and no aphids survived concentrations above 50 ppm. Development time was extended at 12.5 ppm and above. Reductions in fecundity and r_m became statistically significant by 25 ppm. Topical application of benomyl at 100 ppm or above increased aphid mortality, which reached 97% at 400 ppm. Weight gain of aphids was also reduced by topical application at 100 ppm. A factorial experiment showed absence of interaction between the effects on aphid weight of soil drench application to plants and topical application to aphids.     

Penetration of the eastern subterranean termite into soil treated at various thicknesses and concentrations of Dursban TC and Premise 75

The ability of eastern subterranean termites, Reticulitermes flavipes (Kollar), to penetrate various concentrations and treatment thicknesses ranging from 1.0 to 50.0 mm of Dursban TC and Premise 75 was evaluated in a laboratory bioassay. Termites penetrated only a few millimeters into 500 ppm Dursban TC-treated soil at all thicknesses. As concentration decreased, termite penetration into Dursban TC-treated soil increased with termites generally penetrating completely through 5.0- and 0.5-ppm treatments. Termites penetrated at least 30% into 10-, 25-, and 50-mm thicknesses of 100 ppm Premise 75. Termites generally completely penetrated all concentrations < or = 100 ppm and thicknesses < or = 5 mm. At 7 d, termite mortality was 100% at all treatment thicknesses of Dursban TC at 500 and 50 ppm. At 5.0 and 0.5 ppm Dursban TC, termite mortality ranged from approximately 45 to 98% across all treatment thicknesses. At 100- and 10-ppm concentrations of Premise 75-treated soil, termites suffered > or = 75% mortality. Premise 75 at 1.0 and 0.1 ppm generally killed < or = 50% of the assayed termites at all treatment thicknesses.     

Oxidation of ethylene by soil bacteria

The course of the biological oxidation of ethylene by soil was dependent on the type of soil used as well as on other factors. As evidenced from an increase in oxidation rate, the ethylene-consuming microorganisms in soil could grow at the expense of ethylene, even when the gas was present at concentrations of 50 ppm or less. Five strains of bacteria strongly resembling each other were isolated from different soils. These pleomorphic, gram-positive, acid-fast, obligate aerobic, ethylene-oxidizing bacteria grew also on saturated alkanes and on ordinary carbon sources. An apparent K_m for ethylene of approximately 40 ppm was estimated for whole-cell suspensions of strain E20 by following the disappearance of the gas from the atmosphere.     

Interaction Between Nickel and Protein Source in the Ruminant

Eighty growing steers were used to determine the effect of nickel supplementation on performance and metabolic parameters of steers fed corn silage-based diets supplemented with different crude protein sources. Crude protein sources examined included: (1) soybean meal, (2) blood meal, (3) urea, and (4) blood meal-urea (two-thirds of supplemental nitrogen from blood meal and one-third from urea). The protein sources differed in ruminal degradability, nitrogen solubility, and nickel content. Nickel was added within each protein treatment to supply either 0 or 5 ppm of supplemental nickel. The experiment was 84 d in duration and rumen fluid and blood samples were collected on days 42 and 80. Average daily gain and feed efficiency were not affected by nickel supplementation. The addition of 5 ppm supplemental nickel greatly increased rumen bacterial urease activity regardless of protein source. When samples were collected prior to feeding on day 80, nickel increased serum urea nitrogen concentrations in steers fed urea, but decreased circulating urea concentrations in animals fed blood meal or the blood meal-urea combination.Ad libitum intake of trace mineral salt was greatly reduced in steers receiving 5 ppm supplemental nickel. The present study suggests that the source of protein may influence ruminant responses to dietary nickel.     

土壤镉污染与作物

通过土壤镉污染对作物影响的盆栽模拟试验,以揭示重金属镉在土壤—植物系统中的转移、分布规律及其对植物生长、发育的影响。试验证明不同化合形态的镉施入土壤(砂壤质褐土,pH值8.2),水稻对镉吸收的多寡依次为CdCl2>CdSO4>CdO>CdS>CdCO3。白菜的镉吸收表现为CdSO4>CdCl2>CdO>CdCO3。土壤的不同镉浓度(施加CdCl2,以纯镉计)对作物影响的试验结果表明,可食部位达到食品污染标准(谷物含镉量0.4ppm、蔬菜0.2ppm为暂定标准)时的土壤镉污染临界值分别为：小麦、莴苣、白菜<1ppm,茄子、萝卜<2.5ppm,番茄、菜豆<20ppm。土壤因子的处理影响镉的活动性;降低土壤pH值,水稻的镉吸收增加。增施有机肥、ZnSO4、S、CaO、CaSO4可降低糙米含镉量13.4%一30%。白菜的镉吸收,由于增施有机肥、FeSO4、Fe2O3、CaO或S而降低菜叶含镉量28%一61%。以Cd,Zn比1:100或1:200施入土壤,叶内含镉量分别下降61%和76.4%,但白菜产量减少61%和76%。     

Effects of glyphosate on cellulose decomposition in two soils

Glyphosate with an equivalent concentration of either 0, 2.16 or 8.64 kg/hm² was sprayed on to cellulosic materials before burying in two soil types; peat (soil I) and sandy clay loam (soil II). Alternatively the soils were sprayed with 0, 20 or 150 ppm of the herbicide before burying the cellulosic material either immediately or after preincubation for 4 weeks. In soil I, the increase in glyphosate concentrations substantially reduced the decomposition of cellulosic material regardless of the method of application employed. Glyphosate at 8.64 kg/hm² reduced the mass loss of the treated substrate by 83%. However, cellulose decomposition in soil preincubated for 4 weeks before burying was affected almost to the same extent as the untreated control. Glyphosate stimulated cellulose decomposition when substrates were buried in soil II. Mass loss in soil treated with 150 ppm increased by about 100% while when glyphosate was sprayed directly to the substrate (at 8.64 kg/hm²), the loss was about 25%.     

Phytophthora root-rot of container-grown citrus as affected by foliar sprays and soil drenches of phosphorous and acetyl salicylic acids

Mycelial growth ofPhytophthora nicotianae var.parasitica in vitro was inhibited by phosphorous and acetyl salicylic acids at 10 ppm; mycelial growth ofP. citrophthora was inhibited by phosphorous acid at 10 ppm and acetyl salicylic acid at 100 ppm. Foliar sprays and soil drenches with these chemicals were compared with soil applications of metalaxyl as treatments for Phytophthora root-rot of container-grown citrus (var. Cleopatra mandarin) caused by the aforementioned spp. Foliar sprays with 0.1% phosphorous acid were as effective as the metalaxyl treatment in promoting root growth and phosphorous acid offers considerable potential as an alternative treatment for Phytophthora root-rot of citrus.     

Efficiency of rice fertilization schedules including cyanobacteria under soil application of phosphate and molybdate

Productive tillering, grain and straw yields and N-contents of indica rice IR-28 were increased more by urea fertilizer at 48 or 96 kg N/ha along with Inoculation by cyanobacteria than by using 144 kg N/ha without inoculation. Fertilizer N-use efficiency was increased by the cyanobacteria and decreased with increasing amount of urea fertilizer. Further enhancement was obtained by soil application of calclum superphosphate at 36 kg P₂O₅/ha or sodium molybdate at 1 ppm Mo along with cyanobacteria and/or urea. Application of phosphate, however, slightly diminished the enhancement by molybdate.The author is with the Sakha Agricultural Research Station, Kafr El-Sheikh, Egypt.     

Pratylenchus penetrans (Cobb) Populations as Influenced by Microorganisms and Soil Amendments

Numbers of Pratylenchus penetrans in sterilized soil decreased significantly 2 weeks after the addition of 1% w/w (700 ppm N) nonsterile soybean meal (SBM), or sterilized SBM in combination with selected microorganisms. Sterilized SBM had no effect on nematode populations in steamed soil. Bacteria and fungi in the presence of SBM were more effective than the actinomycetes tested, causing up to 96-100% reduction in nematode populations. Simpler nitrogenous compounds included KNO₂, Ca(NO₃)₂, NH₄NO₃, (NH₄)₂CO₃, urea, and peptone, decreased nematode populations with variable effectiveness when added to steamed soil at 700 ppm N; KNO₂ was the most nematicidal.     

Arsenic Contamination in Agricultural Soil Reduces Metabolic Activity of Total and Free-Living Nitrogen-Fixing Bacteria as Revealed by Real-Time qPCR

Laboratory microcosms were used to assess the impact of arsenic (As) contamination on agricultural soil bacterial activity focusing free-living nitrogen fixers for three months. Periodically collected microcosm samples were analyzed by RT–qPCR following extraction of total RNA and cDNA preparation for assessing the metabolically active bacterial population. RT–qPCR data showed the gradual increase of 16S rRNA and nifH gene expression, and relative activity of diazotrophs in the enriched soil bacterial consortia under short time As exposure up to 20 ppm and 10 ppm, respectively. A similar trend of these variables was also noticed but up to 1 ppm As when incubating the bulk soil for the same duration. Reduced bacterial activity was noticed at higher concentration of As although in short time exposure. Extending the As exposure time, the bacterial activities in both enriched consortia and bulk soil were decreased. Although, the relative activity of diazotrophs in enriched consortia was increased in presence of 10 ppm As, the same was decreased in bulk soil when exposed to >1 ppm As for long time indicating susceptibility of nitrogen fixer to As contamination in soil. PCA of the data obtained also indicated a negative correlation between As concentrations and diazotrophic activity.     

Effect of pollutants on the ergosterol content as indicator of fungal biomass

Ergosterol content was determined in 20 white-rot fungi isolates and the values ranged from 2380 to 13 060 μg g⁻¹ fungal biomass. Significant changes of ergosterol content according the physiological stage for Bjerkandera adusta 4312 and Coriolopsis gallica 8260 were found, showing the highest values during the stationary phase. However, in the case of Phanerochaete chrysosporium 3642, no changes were detected during growth. The effect of pollutants, such as heavy metals and fungicides, on the ergosterol content of C. gallica was determined. Heavy metals (Cu 80 ppm, Zn 50 ppm or Cd 10 ppm) and fungicides (thiram 3 ppm or pentachlorophenol 1.5 ppm) at concentrations that reduce the metabolic activity between 18% and 53% (pollutant-stressed cultures) did not affect the ergosterol content. Only the fungicide zineb (25 ppm) reduced significantly the ergosterol content in biomass basis. In soil experiments with Cu (80 ppm) or thiram (10 ppm) after 15 and 30 days of incubation, the ergosterol content in soil was linearly correlated to the fungal biomass C in both polluted and control soil cultures. The ergosterol content was independent of the presence or the absence of pollutants. Thus, these results indicate that ergosterol can be a useful indicator for fungal biomass in polluted soils, and can be applied for monitoring bioremediation processes.     

Individual and combined effects of berberine and santonin on spore germination of some fungi

Berberine and santonin were isolated from rhizomes ofBerberis aristata and unexpanded flower buds ofArtemisia maritima, respectively. Efficacy of these two chemicals individually as well as of their mixtures, was tested against spore germination of some saprophytic and obligate fungi. While berberine individually was effective against most of the fungi,Helminthosporium spp. were least affected even at the highest dose (1500 ppm). Santonin was equally effective against several fungi. Mixture of both alkaloids found to be more effective than individual ones. Keeping the dose of berberine constant and santonin at two different concentrations (viz. 250 and 500 ppm) the spore germination ofHelminthosporium, oryzae was stimulated. Increasing concentration of santonin inhibited the spore germination of all other fungi tested,Colletotrichum capsici being affected only by 20 and 5% (at berberine concentration of 250 and 500 ppm, respectively). On the other hand, santonin being constant and berberine at different concentrations, the mixture was effective against all the fungi.     

脲酶抑制剂氢醌对大豆结瘤、固氮和木质部溶质氮形态的影响

首次报导了在白浆土和砂壤土上使用氢醌(HQ)抑制土壤脲酶活性,有效地缓解尿素分解产物及其随后的氧化产物对大豆结瘤和固氮活性的抑制效应,结果表明:1.HQ浓度在40PPM以内对大豆幼苗生长及初生结瘤表现促进作用;进一步提高HQ浓度将使大豆根系生长受阻变态而阻止结瘤。2.HQ(10—50PPM)提高了离体活性大豆根瘤类苗体悬液的耗氧量(79.4—86.1％)和琥珀酸脱氢酶活性(124.7—138.4％)。3.盆栽和田间试验证实,由于HQ缓解了尿素的分解,从而颇大减轻了尿素对大豆结瘤和固氮(乙炔还原活性)的抑制效应;通过大豆木质部中溶质氮形态(酰胺、酰脲和硝酸盐)的分析进一步证实了,大豆植株从根部向地上部运输的氮素形态同土壤氮转化强度和根瘤固氮强度(酰脲相对丰度)之间的紧密联系。4.由于麦秸还田土壤脲酶活性提高,故应提高HQ剂量;与此同时,通过麦秸的“氮因子效应”便能完全解除尿素对大豆结瘤固氮的抑制,并为大豆籽实发育提供了丰富的土壤氮源。