Evaluation of soil solar heating for control of damping-off fungi in two forest nurseries in France

Field experiments were carried out at two different forest nurseries during the summer of 1994 to examine the efficacy of soil solarization for the control of damping-off. Both soils hosted Pythium spp., Fusarium spp. and Rhizoctonia solani as damping-off agents. Soil samples from solarized, steamed, fumigated and untreated plots were periodically collected and assayed for soil infectivity. Solarization with a double layer of polyethylene film was as effective as steaming or fumigation in reducing soil infectivity in the uppermost layer. During July the temperature of covered beds rose as high as 50°C at a soil depth of 5cm. The method achieved good control of Pythium spp., the main cause of damping-off at both nurseries, whereas Fusarium spp. were more tolerant. The association of Trichoderma spp. with a reduction of soil infectivity at the last sampling date strongly suggested that biocontrol processes were induced after solarization. Soil solarization provides a suitable method for control of damping-off. Received: 29 October 1996     

Displacement of native rhizobia nodulating chickpea (Cicer arietinum L.) by an inoculant strain through soil solarization

Summary Soil solarization greatly reduced the native chickpea Rhizobium population. With inoculation, it was possible to increase the population of the Rhizobium in solarized plots. In the 1st year, 47% nodulation was obtained with chickpea inoculant strain IC 59 when introduced with a cereal crop 2 weeks after the soil solarization and having a native Rhizobium count of <10 g^-1 soil, and only 13% when introduced 16 weeks after solarization at the time the chickpeas were sown, with 2.0×10² native rhizobia g^-1 soil. In the non-solarized plots inoculated with 5.6×10³ native rhizobia g^-1 soil, only 6% nodulation was obtained with the inoculant. In the succeeding year, non-inoculated chickpea was grown on the same plots without any solarization or Rhizobium inoculation. The treatment that showed good establishment of the inoculant strain in year 1 formed 68% inoculant nodules. Other treatments indicated a further reduction in inoculant success, from 1%–13% to 1%–9%. Soil solarization thus allowed an inoculant strain to successfully displace the high native population in the field and can serve as a research tool to compare strains in the field, irrespective of competitive ability. In year 1, Rhizobium inoculation of chickpea gave increased nodulation and increased plant growth 20 and 51 days after sowing, and increased dry matter, grain yield, and grain protein yield at maturity. These beneficial effects of inoculation on plant growth and yield were not measured in the 2nd year.Submitted as Journal Article No. JA 945 by the International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Patancheru, Andhra Pradesh 502 324, India     

Biological control of Rhizoctonia sp. root rot of Casuarina equisetifolia seedlings by Frankia spp. strains

Seventy Frankia spp. strains (nodulating N₂-fixing actinomycetes) were isolated from root nodules of Casuarina equisetifolia from different localities of Tamil Nadu state, India. From these, four strains (UMCe12, UMCe23, UMCe35, and UMce55) were selected. Their potential use as biological control agents for Rhizoctonia solani root rot disease of C. equisetifolia seedlings and their relative efficiency in nodule production were investigated. Between the two inoculum broadcast systems tested, seed-coating with Frankia spp. cell suspension was superior to the soil application of cells as sand-vermiculite-basal ammonium propionate inoculum. UMCe12 was the promising strain, offering the highest level of disease protection (81.1%) and nodule production (88.1%) in the R. solani-infested soil, followed by UMCe23 (60.3 and 65.5% of disease protection and nodule production, respectively), UMCe55 (53.5 and 58.2%), and UMCe35 (45.4 and 44.5%). Further, a significant positive correlation was observed between the dose of Frankia spp. and efficiency in both disease control and nodule production.     

Soil solarization: Effects on soil properties,crop fertilization and plant growth

Summer solarization of six wet field soils of four different textures raised soil temperatures by 10–12°C at 15cm depth. Soil solarization increased concentrations of NO^?₃N and NH⁺₄N up to six times those in nontreated soils. Concentrations of P, Ca²⁺, Mg²⁺ and electrical conductivity (EC) increased in some of the solarized soils. Solarization did not consistently affect available K⁺, Fe³⁺, Mn²⁺, Zn²⁺, Cu²⁺, Cl^? concentrations, soil pH or total organic matter. Concentrations of mineral nutrients in wet soil covered by transparent polyethylene film, but insulated against solar heating, were the same as those in nontreated soil. Increases in NO^?₃N plus NH⁺₄N were no longer detected in fallowed soils 9 months after solarization. No significant correlation between mineral-nutrient concentration in plant tissue and plant growth was found. Fresh and dry weights of radish, pepper and Chinese cabbage plants usually were greater when grown in solarized soils than in nontreated soils. Fertilization of solarized soils sometimes resulted in greater plant growth responses than observed in solarized but nonfertilized soils.     

Microbial community response to soil solarization in Nepal's rice-wheat cropping system

The Indo-Gangetic Plains of South Asia support 13.5 million hectares of rice-wheat cropping systems, which currently feed over one billion people. Intensified agriculture has resulted in a more than two-fold increase in rice and wheat yields since the 1970s; however, this continuous cropping has also exacerbated weed, pest and disease problems. Soil solarization is an accessible, low-risk management practice for small-holder farmers that has ameliorated these problems in some settings and has the potential to dramatically improve yields. Field trials were conducted at two sites in Nepal to test whether soil solarization: (i) had a lasting effect on soil bacterial, fungal and nematode communities; (ii) altered the rhizosphere communities of rice nursery seedlings and (iii) improved crop growth and yield in the rice-wheat cropping system. Rice seedlings were grown in nursery plots that were solarized for 28 days or left untreated and were transplanted to field plots that were also either solarized for 28 days or not in a randomized complete block design with four replications. Rice was grown to maturity and harvested, followed by a complete wheat cropping cycle. Solarization of main field plots increased counts of fungal propagules and decreased root galling and nematode counts and decreased weed biomass. Terminal restriction fragment length polymorphism (T-RFLP) analyses of extracted soil DNA revealed significant shifts in fungal community composition following soil solarization, which was sustained throughout the entire rice cropping cycle at both field sites. The bacterial community composition was similarly affected, but at only one of the two sites. Despite the observed changes in soil microbial community composition over more than one cropping period, solarization had no impact on crop productivity at either site. Nevertheless, such changes in soil microbial communities in response to solarization may be responsible for increased yields observed at other sites with greater pathogen pressure. This practice has shown promising results in many farmers’ fields in South Asia, but further elucidation of the mechanisms by which solarization increases productivity is needed.     

不同连作年限马铃薯根系分泌物的成分鉴定及其生物效应

为探讨马铃薯连作障碍的可能机理,在大田条件下,收集连作1～5 a(CP1-CP5)马铃薯植株的根系分泌物,采用GC-MS对根系分泌物的主要成分进行了鉴定,并通过生物检测验证了根系分泌物的生物效应。结果表明:CP1-CP5鉴定出的物质主要有酸类、糖类、胺类、醇类、酯类和嘧啶类,但各类物质的数量和含量不同。CP1-CP5中均鉴定出棕榈酸,相对含量分别为0.55%、0.87%、1.24%、1.05%和0.95%,浓度分别为7.12 mg×L~(-1)、7.39 mg×L~(-1)、9.46 mg×L~(-1)、8.38 mg×L~(-1)和8.02 mg×L~(-1)。马铃薯根系分泌物显著抑制了马铃薯的生长,抑制作用随连作年限延长而增强。棕榈酸对马铃薯生长的抑制表现出明显的浓度效应,随浓度升高而增强。马铃薯根系分泌物明显促进了立枯丝核菌的生长,菌落直径和菌丝鲜质量表现为CP3最高,CP1最低,CP2、CP4和CP5之间没有显著差异。棕榈酸明显促进了立枯丝核菌的生长,随着棕榈酸浓度的增加,菌落直径和菌丝鲜质量先增加再减小, 10 mg×L~(-1)棕榈酸的菌落直径和菌丝鲜质量最大。由此说明,随马铃薯连作年限延长,根系分泌物的毒性越强;马铃薯根系分泌物对立枯丝核菌的促进作用加剧了马铃薯的连作障碍,棕榈酸是马铃薯根系分泌的化感自毒物质。     

Soil Solarization: An Organic Weed-Management Approach in Cauliflower

Studies were conducted at KPK Agricultural University, Peshawar, Pakistan, in June 2008 and 2009 using a randomized complete block design. Plots were covered with transparent polyethylene films for different periods (0, 2, 4, 6, 8, and 10 weeks). The temperature inside the film was about 10 °C greater than the atmospheric temperature. Solarization increased nitrogen (N) and organic-matter levels in both years, probably because of decomposition of plant residues. Increasing the period of solarization decreased weed density and both fresh and dry biomass. The effectiveness of solarization was species specific. In 2008, Cirsium arvense L. was controlled in the solarized soil, whereas Vicia sativa germination was stimulated by solarization. In 2009, suppressed weeds included Sorghum halepense whereas Chenopodium album L., Cyperus rotundus, and Rumex crispus L. were unaffected. Solarization increased yield of cauliflower (Brassica oleracea L.) in both years. These results suggest that solarization should be practiced before planting horticultural crops in areas with a hot climate.     

Enhanced denitrification in plots of N2-fixing faba beans compared to plots of a non-fixing legume and non-legumes

Denitrification rates were studied using the C₂H₂ inhibition technique in a 2-year field experiment within plots of nodulated and non-nodulated faba beans, ryegrass, and cabbage. Denitrification rates ranged from 14.40 to 0.02 ng N₂O–N g^–1 soil dry weight h^–1. Mean denitrification increased fourfold in plots of N₂–fixing Vicia faba compared to non-nodulated V. faba mutant F48, Lolium perenne, and Brassica oleracea. The results with and without C₂H₂ treatment indicate that in the field the major part of this enhanced denitrification led to the endproduct N₂ rather than to the ozone-degrading N₂O. Higher denitrification rates of plots with N₂–fixing plants in September seemed to be caused by an increase in soil NO _inf3 ^sup- of about 20 kg ha^–1 found between July and August. Soil NO _inf3 ^sup- and soil moisture explained 67% of the variation in denitrification rates of the different soil samples over the growing seasons in the 2 years. Soil moisture explained 44% of the variation for soil planted with N₂–fixing plants and 62% for soil planted with non-fixing plants. Positive exponential relationships were obtained between denitrification rates and soil nitrate (r=0.71) and soil moisture (r=0.82).     

A novel method for the identification and enumeration of microorganisms with potential for suppressing fungal plant pathogens

This paper describes a method that allowed counting of both the total culturable and antagonistic microorganisms in a given source such as compost. Fusarium solani, used as the test fungus, was spread-plated on quarter-strength (1/4) potato dextrose agar (PDA), its surface was exposed in a laminar flow for 4 h and then another layer (2–3 mm thick) of 1/4 PDA was poured over it, on which an appropriate dilution of a compost sample was spread-plated. Microorganisms in the compost samples appeared first, and were counted as total culturable organisms. Plates were further incubated until F. solani grew through the upper layer of PDA (generally in 4–8 days) and covered the whole plate including most of the microbial colonies, except for a few which had a halo around them. These were counted as antagonistic, and they were isolated and purified for further studies. The population of bacteria in the six specific compost samples (called Biodynamic or BD preparations by organic farmers) ranged from 3.45 log₁₀ (in BD502) to 8.59 log₁₀ (in BD504) per gram of materials. The population of antagonistic bacteria was counted for three of the six compost samples, and ranged from 3.24 log₁₀ (in BD502) to 6.90 log₁₀ (in BD500). Of the 67 bacterial isolates showing a halo that were assembled from different sources, 17 suppressed at least 1 of the 4 plant pathogenic fungi against which these were evaluated using the dual culture method.     

The Effects of Soil Solarization and Compost on Soil Suppressiveness against Fusarium Oxysporum f. sp. Melonis

Soil suppressiveness against Fusarium was tested using solarized and non-solarized soils combined with composts of three maturation levels, and a non-amended control. The soils were sampled on three dates: after previous year solarization but before current year solarization (0 weeks), at the end of the solarization period of the current year (4 weeks), and 4 weeks later (recovery time). Melon seedlings were inoculated with Fusarium spores and disease severity was assessed. The study showed a reduction of soil suppressiveness capacity against Fusarium oxysporum f. sp. melonis after 1 year of solarization (0 weeks). Fusarium disease severity in artificially inoculated melon plants, expressed by area under the disease progress curve, was higher in solarized soil than in non-solarized soil. Compost addition lowered the disease severity, both in the solarized and in the non-solarized soils. However, suppression was not obtained at the end of the solarization period, whereas compost beneficial effect was found at this time.     

Inactivation of Escherichia coli in soil by solarization

Abstract

Contamination of agricultural soil by fecal pathogenic bacteria poses a potential risk of infection to humans. For the biosafety control of field soil, soil solarization in an upland field was examined to determine the efficiency of solarization on the inactivation of Escherichia coli inoculated into soil as a model microorganism for human pathogenic bacteria. Soil solarization, carried out by sprinkling water and covering the soil surface with thin plastic sheets, greatly increased the soil temperature. The daily average temperature of the solarized soil was 4–10°C higher than that of the non-solarized soil and fluctuated between 31 and 38°C. The daily highest temperature reached more than 40°C for 8 days in total in the solarized soil during the second and third weeks of the experiment. Escherichia coli in the solarized soil became undetectable (< 0.08 c.f.u. g^?1 dry soil) within 4 weeks as a result, whereas E. coli survived for more than 6 weeks in the non-solarized soil. Soil solarization, however, had little influence on the total direct count and total viable count of bacteria in the soil. These results indicate that soil solarization would be useful for the biosafety control of soil contaminated by human pathogens via immature compost or animal feces.     

Impact of soil solarization on the ciliate community structure of a greenhouse soil

Soil solarization is an ecologically friendly method of controlling various plant pathogens and pests, but also affects non-pathogenic members of the soil biota. Here, we studied the impact of soil solarization on the community structure of soil ciliates using a culture-independent molecular approach, namely denaturing gradient gel electrophoresis (DGGE) of targeted 18S rRNA gene fragments. Greenhouse soil with added organic fertilizers was solarized for 33 days at an average temperature of 47–48°C. Solarization caused a drastic change in the ciliate community. The variation between replicates was large, which suggested that the distribution of ciliates was spatially heterogeneous in the soil, probably due to their decreased numbers. In contrast, non-solarized soil had a stable and homogeneous ciliate community during the experimental period. In solarized soil, most of the original ciliate community recovered 76 days after solarization. Sequence analysis of DGGE fragments indicated that both r-selected and K-selected species of ciliates were affected by solarization but recovered with time after solarization. Our results demonstrated both the vulnerability and resilience of the ciliate community to soil solarization and also the utility of using molecular-based analysis of ciliate communities as bioindicators of soil stress caused by solarization.     

Use of 15N isotope dilution for quantification of N2 fixation associated with roots of kallar grass (Leptochloa fusca (L.))

Summary Leptochloa fusca (L.) Kunth (kallar grass) has previously been found to exhibit high rates of nitrogen fixation. A series of experiments to determine the level of biological nitrogen fixation using ¹⁵N isotopic dilution were carried out in nutrient solution and saline soil. In the nutrient solution, E. coli inoculated plants were taken as non-nitrogen-fixing control. It was observed that nearly 60%–80% of the plant N was derived from atmospheric fixation. Estimations based on the N difference method gave much lower values (18%–35%). In experiments with saline soil which was initially sterilized with chloroform fumigation, a mixed culture of N₂-fixing rhizospheric isolates from kallar grass roots was inoculated and planted to kallar grass. Uninoculated treatments were regarded as controls. The soil was previously labelled with ¹⁵N by adding cellulose and (¹⁵NH₄)₂SO₄. The results of these studies showed fixation values of 6%–32% when estimated by ¹⁵N dilution, whereas by the N difference method 54% of the plant N was estimated to be derived from fixation. This discrepancy is due to the increase in root proliferation due to inoculation, which results in greater uptake of soil N. The distribution of ¹⁵N in different fractions of the soil-N indicted isotopic dilution due to bacterial fixation of atmospheric N₂.     

Fluctuations in the abundance of ammonia oxidizers and the contents of inorganic nitrogen in solarized soil

Solarization makes a great impact on the abundance of ammonia oxidizers and nitrifying activity in soil. To elucidate fluctuations in the abundance of ammonia oxidizers and nitrification in solarized soil, copy numbers of amoA gene of ammonia-oxidizing bacteria (AOB) and archaea (AOA), viable number of ammonia oxidizers and inorganic nitrogen contents were investigated in greenhouse experiments. The copy number of amoA gene and the viable number of ammonia oxidizers were determined by the quantitative polymerase chain reaction and most probable number methods, respectively. Abundance of AOB based on the estimation of amoA gene copy numbers and viable counts of ammonia oxidizers was decreased by the solarization treatment and increased during the tomato (Solanum lycopersicum L.) cultivation period following the solarization. Effect of solarization on the copy number of amoA gene of AOA was less evident than that on AOB. The proportion of nitrate in inorganic nitrogen contents was declined by the solarization and increased during the tomato cultivation period following the solarization. Positive correlations were found between the proportion of nitrate in inorganic nitrogen content and the copy number of bacterial or archaeal amoA gene or the viable number of ammonia oxidizers; the copy number of bacterial amoA gene showed a strong correlation with the viable number of ammonia oxidizers. The present study revealed influences of solarization on the fluctuation in the abundance of ammonia oxidizers and dynamics of inorganic nitrogen contents in soil and the results indicate that the determination of amoA gene of AOB is possibly a quick and useful diagnostic technique for evaluating suppression and restoration of nitrification following solarization.     

Ant-induced soil modification and its effect on plant below-ground biomass

Lasius flavus is a dominant mound-building ant species of temperate grasslands that significantly modifies soil parameters. These modifications are usually the result of workers’ activities such as food accumulation and nest construction. An alternative hypothesis that could explain changes in soil is colony founding in areas of higher soil fertility.In our study we investigated several soil parameters sampled in 10 ant nests and adjacent (control) plots in mountain grassland in Slovakia. The alternative hypothesis was tested by comparing occupied and abandoned mounds. While we found increased concentrations of available P and K in the nests, concentrations of total C, total N, Ca²⁺ and Mg²⁺ were lower there. We propose that differences found between the soil of nests and control plots are entirely a product of ant activity during mound occupancy and not due to initial soil differences during nest establishment. This was confirmed by the comparison of occupied and abandoned nests in which the soil fertility of abandoned nests was similar to conditions in the surrounding soil.Along with the modification of soil chemistry, we recorded changes in soil physical properties and the vertical distribution of nutrients. Ant nests were characterized by the dominance of 0.02–0.1 mm particles and lower bulk density. In the same habitat, nutrient concentrations did not change along the vertical gradient in contrast to control plots where soil nutrients decreased and bulk density increased with depth. Root biomass followed the vertical pattern observed with nutrients: in control plots, most roots were concentrated in the uppermost layer (0–3 cm), whereas they were evenly distributed along the vertical gradient in the nests. We also found that rhizome internodes of Agrostis capillaris were thinner and longer in plants from the mounds. Changes in soil physical properties, vertical distribution of nutrients and root biomass in the nests are most probably a consequence of mounding and soil mixing (bioturbation), which has been less reported on in ant-soil studies.     

Sesbania rostrata as a green manure for lowland rice: Growth,N2 fixation,Azorhizobium sp. inoculation,and effects on succeeding crop yields and nitrogen balance

Summary Root and stem nodulation, nitrogen fixation (acetylene-reducing activity), growth and N accumulation bySesbania rostrata as affected by season and inoculation were studied in a pot experiment. The effects ofS. rostrata as a green manure on succeeding wet-season and dry-season rice yields and total N balance were also studied.S. rostrata grown during the wet season showed better growth, nodulation, and greater acetylene-reducing activity than that grown during the dry season. Inoculation withAzorhizobium caulinodans ORS 571 StrSpc® (resistant to streptomycin and spectinomycin) on the stem alone or on both root and stem significantly increased N₂ fixation by the plants. Soil and seed inoculation yielded active root nodules under flooded conditions. Plants that were not inoculated on the stem did not develop stem nodules. The nitrogenase activity of the root nodules was greater than that of the stem nodules in about 50-day-oldS. rostrata. S. rostrata incorporation, irrespective of inoculation, significantly increased the grain yield and N uptake of the succeeding wet season and dry season rice crops. The inoculated treatments produced a significantly greater N gain (873 mg N pot^–1) than the noinoculation (712 mg N pot^–1) treatment. About 80% of the N gained was transferred to the succeeding rice crops and about 20% remained in the soil. The soil N in the flooded fallow-rice treatment significantly declined (–140 mg N pot^–1) but significantly increased in bothS. rostrata-rice treatments (159 and 151 mg N pot^–1 in uninoculated and inoculated treatments respectively). The N-balance data gave extrapolated values of N₂ fixed per hectare at about 303 kg N ha^–1 per two crops forS. rostrata (uninoculated)-rice and 383 forS. rostrata (inoculated)-rice.     

Increased emergence of spring wheat after inoculation with Pseudomonas chlororaphis isolate 2E3 under field and laboratory conditions

Inoculation at the time of planting with Pseudomonas chlororaphis strain 2E3 increased the emergence of spring wheat by 8% and 6% at two different sites in northern Utah. Isolate 2E3 strongly inhibited the growth of the wheat pathogen Fusarium culmorum on artificial media. A second isolate of P. chlororaphis (strain O6) also inhibited fungal growth on artifical media but did not increase emergence of the spring wheat at the same field sites. Inoculation of winter wheat by 2E3 did not promote emergence when planted into field soil sterilized by fumigation with methyl bromide. Under laboratory conditions, emergence of spring wheat in sterilized soils from both sites was at least 90%. In the soils that were not sterilized, emergence was below 25% in soil from one site and below 50% in soil from the other. Treating seeds with 2E3 significantly improved emergence in a sterile soil-containing matrix that had been inoculated with the wheat pathogen Fusarium culmorum. Consequently, we propose that increases in wheat emergence can be attributed to the suppression by 2E3 of pathogenic organisms present in the native field soils. A strain of Rhizoctonia solani, shown to the pathogenic on winter wheat, was isolated from one of these soils.     

Mycorrhizae, biocides, and biocontrol 3. Effects of three different fungicides on developmental stages of three AM fungi

The effects of biocide use on nontarget organisms, such as arbuscular mycorrhizal (AM) fungi, are of interest to agriculture, since inhibition of beneficial organisms may counteract benefits derived from pest and disease control. Benomyl, pentachloronitrobenzene (PCNB) and captan were tested for their effects on the germination and early hyphal growth of the AM fungiGlomus etunicatum (Becker & Gerd.),Glomus mosseae (Nicol. & Gerd.). Gerd. and Trappe andGigaspora rosea (Nicol & Schenck) in a silty-clay loam soil placed in petri plates. Application of fungicides at 20 mg active ingredient (a.i) kg^–1 soil inhibited spore germination by all three AM-fungal isolates incubated on unsterilized soil for 2 weeks. However, fungicides applied at 10 mg a.i. kg^–1 soil had variable effects on AM-fungal isolates. Fungicide effects on germination and hyphal growth of G.etunicatum were modified by soil pasteurization and CO₂ concentration in petri plates and also by placing spores below the soil surface followed by fungicide drenches. Effects of fungicides on mycorrhiza formation and sporulation of AM fungi, and the resulting host-plant response, were evaluated in the same soil in associated pea (Pisum sativum L.) plants. Fungicides applied at 20 mg a.i. kg^–1 soil did not affect the root length colonized byG. etunicatum, but both benomyl and PCNB reduced sporulation by this fungus. Benomyl and PCNB reduced the root length colonized byG. rosea at 48 and 82 days after transplanting. PCNB also reducedG. mosseae-colonized root length at 48 and 82 days, but benomyl only affected root length colonized byG. mosseae at the earlier time point. Only PCNB reduced sporulation byG. mosseae, consistent with its effect on root length colonized by this fungus. captan reduced the root length colonized by G. rosea at 48 days, but not at 82 days, and reduced colonization byG. mosseae at 82 days, but not at 48 days. Captan did not affect sporulation by any of the fungi.G. rosea spore production was highly variable, but benomyl appeared to reduce sporulation by this fungus. Overall,G. etunicatum was the most tolerant to fungicides in association with pea plants in this soil, andG. rosea the most sensitive. Benomyl and PCNB were overall more toxic to these fungi than captan. Interactions of AM fungi and fungicides were highly variable and biological responses depended on fungus-fungicide combinations and on environmental conditions.     

Influence of oxygen on denitrification and aerobic respiration in soil

Summary The influence of the partial pressure of oxygen on denitrification and aerobic respiration was investigated at defined P02 values in a mull rendzina soil. The highest denitrification and respiration rates obtained in remoistened, glucose- and nitrate-amended soil were 43 1 N₂0 h^–1g^–1 soil and 130 1 O₂ h^–1g^–1 soil, respectively. At -55 kPa matric water potential, corresponding to 40% water saturation, N₂0 was produced only below P0₂ 40 hPa. The K _m, for O₂ was 3.0 x 10^–6 M. Formation of N₂O and consumption of O₂ occurred simultaneously with half maximum rates at P0₂ 6.7–13.3 hPa. Nitrite accumulated in soil below 40 hPa and increased with decreasing pO₂. The upper threshold for N₂0 formation in amended soil was P0₂ 33–40 hPa (39-47 M O₂).     

Effect of time of mulching on soil temperature and moisture regime and emergence, growth and yield of white yam in western Nigeria

Time of mulching can influence the growth environment and performance of white yam (Dioscorea rotundata Poir). An on-farm trial was conducted during the 1988–1989 and 1989–1990 seasons (October–August) in Nigeria to determine the effect of time of mulching (October–February) on the hydrothermal regime and emergence, growth and tuber yield of white yam. Application of 12.5 mg ha⁻¹ of dry Eupatorium odoratum L. (Syn. Chromolaena odorata L.) mulch on top of the mounds significantly improved soil moisture content of the 15 cm surface layer by 50–120 g kg⁻¹ and decreased the maximum soil temperature by 2–7°C at 15 cm depth in the early growing season (March–April). The emergence and development of yam seedlings were significantly lower in unmulched plots than in mulch-treated plots. Mulching significantly increased tuber yield by about 10–15 mg ha⁻¹ season⁻¹. Plots mulched in October–December were more moist by 20–60 g kg⁻¹ and cooler by 1–3°C, and had 27–44% greater emergence than those mulched in January or February. The number of leaves per plant, vine diameter and leaf area index were also significantly greater in plots mulched in October–December than plots mulched in January or February. Consequently, shoot dry weight was about 28–36% greater in yam mulched in October–December than in yam mulched in February. However, the time of mulching had no effect on soil moisture of the surface layer at the beginning of the rainy season (April), on yam emergence in May and on tuber yield and yield components. Although time of mulching did not significantly affect tuber yield, the increase (10–15%) in the tuber yield of yam mulched in December–February compared to the yam mulched in October or November was considerable. It was concluded that yam planted in October, just before the rain stops, can be mulched in January or February without detrimental effect on emergence, growth and tuber yield.