Evaluation of fungicides applied to soil to control naturally-occurring take-all using a balanced-incomplete-block design and very small plots

Six sterol biosynthesis-inhibiting fungicides representing several combinations of properties were applied to soil to control naturally-occurring take-all (caused by Gaeumannomyces graminis var. tritici) in winter wheat in field experiments in two successive years. The average take-all severity category was never more than moderate in the different clay-loam and sandy loam sites used in each year. At each site in each year there were six treatments and an untreated control in an arrangement based on a balanced-incomplete-block design for six treatments in 10 blocks each with three treatments. Each block had three treated plots and a control plot and was paired with the complementary block of three treatments (plus control) to form a complete replicate, of which there were 30 per site. Take-all assessments in June or July showed that after incorporation into the seed bed (at 2 kg ha“¹and sometimes at 1 kg ha”¹) in autumn, two non-volatile, strongly lipophilic compounds, nuarimol and triadimenol, with good intrinsic toxicity to the take-all fungus and slow rates of degradation, partially controlled take-all. However, another compound, flutriafol, with similar properties to nuarimol and triadimenol, controlled take-all less. Two slightly volatile, strongly lipophilic compounds, flusilazole and penconazole, with good intrinsic activity, were less effective (at 2 kg ha^-1). A volatile, less lipophilic compound, PP 969, with less intrinsic activity, also partially controlled take-all, but only after application as a drench in the spring (2 kg ha^-1). The most effective treatments were generally more effective the greater the level of disease (as indicated by assessments of disease in control plots), especially in spring assessments of disease. Although flutriafol did not perform as expected, it still seems reasonable to conclude that the requirements for a soil-applied fungicide to control take-all are likely to be: (i) good intrinsic fungitoxicity, (ii) some mobility in soil water (i.e. not strongly lipophilic), and (iii) season-long persistence.     

Soil-applied fungicides for controlling take-all in field experiments with winter wheat

Soil treatment fungicides were tested against take-all (Gaeumannomyces graminis var. tritici) in three field experiments with winter wheat. Fungicides were applied as drenches either before sowing in autumn, and incorporated by rotary harrowing, or to the crop in spring. The most effective treatments were autumn applied benomyl (20 kg/ha) and nuarimol (0·55-4·4 kg/ha). However, the highest nuarimol concentration depressed yield. Benomyl sometimes induced a resurgence of take-all in the second wheat crop after treatment. Nuarimol had no adverse effects in subsequent crops, and neither fungicide hindered the onset of take-all decline in a third crop after treatment. The possible value of soil treatment in future control strategies is discussed.     

The effect of seed and stem base spray treatment with iprodione on white rot disease (Sclerotium cepivorum) in autumn-sown salad onions

Iprodione applied to seed at 250 g a.i./kg controlled white rot in autumn-sown salad onions until July the following year, and reduced losses during the winter caused by Botrytis spp. At 25–150 g a.i./kg seed, iprodione controlled autumn and spring infections but it was less effective later in the summer. Treatment of autumn-sown onions at 50 g a.i./kg seed followed in March by a single stem base spray at 0.031 g a.i./m row (total rate c. 2.4 kg a.i./ha) gave complete control; seed treatment at 25 g a.i./kg followed by a stem base spray at 0.125 g a.i./m row (c. 4.5 kg a.i./ha) was equally effective. Four stem base sprays of iprodione at 0.075 g a.i./m row/spray (9 kg a.i./ha) applied in spring to plants raised from untreated seed, controlled spring and summer infections but yields were low because of losses caused by infection in the previous autumn. A single stem base spray of iprodione at 0.125 g a.i./m row applied in spring to plants raised from thiophanate-methyl treated seed at 125 g a.i./kg gave complete control and high yields.     

Depletion of Rice as Food of Waterfowl Wintering in the Mississippi Alluvial Valley

ABSTRACT Waterfowl habitat conservation strategies in the Mississippi Alluvial Valley (MAV) and several other wintering areas assume carrying capacity is limited by available food, and increasing food resources is an effective conservation goal. Because existing research on winter food abundance and depletion is insufficient to test this hypothesis, we used harvested rice fields as model foraging habitats to determine if waste rice seed is depleted before spring migration. We sampled rice fields (n = 39 [winter 2000–2001], n = 69 [2001–2002]) to estimate seed mass when waterfowl arrived in late autumn and departed in late winter. We also placed exclosures in subsets of fields in autumn (n = 8 [2000–2001], n = 20 [2001–2002]) and compared seed mass inside and outside exclosures in late winter to estimate rice depletion attributable to waterfowl and other processes. Finally, we used an experiment to determine if the extent of rice depletion differed among fields of varying initial abundance and if the seed mass at which waterfowl ceased foraging or abandoned fields differed from a hypothesized giving-up value of 50 kg/ha. Mean seed mass was greater in late autumn 2000 than 2001 (127.0 vs. 83.9 kg/ha; P = 0.018) but decreased more during winter 2000–2001 than 2001–2002 (91.3 vs. 55.7 kg/ha) and did not differ at the end of winter (35.8 vs. 28.3 kg/ha; P = 0.651). Assuming equal loss to deterioration inside and outside exclosures, we estimated waterfowl consumed 61.3 kg/ha (48.3%) of rice present in late autumn 2000 and 21.1 kg/ha (25.1%) in 2001. When we manipulated late-autumn rice abundance, mean giving-up mass of rice seed was similar among treatments (48.7 kg/ha; P = 0.205) and did not differ from 50 kg/ha (P = 0.726). We integrated results by constructing scenarios in which waterfowl consumed rice at different times in winter, consumption and deterioration were competing risks, and consumption occurred only above 50 kg/ha. Results indicated waterfowl likely consumed available rice soon after fields were flooded and the amount consumed exceeded our empirical estimates but was ≤48% (winters pooled) of rice initially present. We suggest 1) using 50 kg/ha as a threshold below which profitability limits waterfowl feeding in MAV rice fields; 2) reducing the current estimate (130 kg/ha) of rice consumed in harvested fields to 47.1 kg/ha; and 3) increasing available rice by increasing total area of fields managed, altering management practices (e.g., staggered flooding), and exploring the potential for producing second or ratoon rice crops for waterfowl.     

Studies of the cereal cyst-nematode, Heterodera avenae under continuous cereals, 1974–1978. I. Plant growth and nematode multiplication

Population changes of Heterodera avenae and crop growth in a sandy loam soil were studied from 1974 until 1978; the nematode decreased plant growth but failed in two of the years to multiply on susceptible hosts. Spring oats were the most heavily invaded cereal and produced the smallest shoots. Second-stage juveniles invaded cereal roots in decreasing numbers: spring oats > autumn oats > spring barley > spring wheat > autumn barley > autumn wheat. Numbers of females developing on the different cultivars were in a similar order. Most females developed on roots in 1976 despite poor crop growth in the severe drought. Numbers of H. avenae in soil treated with oxamyl (Vydate) at 8.8 kg/ha a. i. were less in all years except 1975. In the dry winter and spring of 1975/76 nematode multiplication was prevented in soil treated with oxamyl before drilling in the autumn. In all years large numbers of females were produced on the roots of all cultivars but in 1975 and 1978 nematode populations declined because few females survived to form cysts containing eggs and their fecundity was reduced. Numbers of cysts after harvest were not affected by formalin (38% formaldehyde) applied as a drench at 3000 litres/ha in 1977 but fecundity doubled in treated soil, and nematode multiplication increased from 3.8 × in untreated plots to 18.6 ×. When the plots were irrigated in 1978 numbers of cysts and fecundity increased in formalin treated soil resulting in an increase in multiplication from 0.3 × to 14.6 ×. Fungal parasites attacking H. avenae females and eggs are considered responsible for the poor multiplication of the nematode.     

Eco-friendly approaches for the management of fenugreek root rot

To evolve eco-friendly management of fenugreek root rot caused by Rhizoctonia solani, a field trial was conducted during Kharif 2002 and Rabi seasons of 2002–2003 and 2003–2004. Experiments were conducted with eight treatments and three replications in RBD using the variety CO-2. The pooled analysis of the three season data showed that seed treatment with Trichoderma viride at 4g/kg of seed + soil application of Trichoderma viride at 5 kg/ha + soil application of neem cake at 150 kg/ha (T₃) recorded a percent disease index (PDI) of 23.1 versus 65.5 PDI in the control which accounted for a disease reduction of 64.7%. It was on par with seed treatment with Trichoderma viride at 4g/kg of seed + soil application of T. viride at 5 kg/ha (T₂) which reduced the disease incidence by 62.3% (24.7 PDI). The chemical treatment used for comparison, i.e. seed treatment with carbendazim + soil drenching at 0.1% + soil application of neem cake at 150 kg/ha recorded the lowest PDI of 16.8 with 74.4% disease reduction. Among the various treatments T₃ gave a seed yield of 572.7 kg/ha followed by T₂ (555.7 kg/ha). Treatment T₇ recorded the highest yield of 578.7 kg/ha. In the control plot the recorded yield was only 359.3 kg/ha. Though T₃ was more effective at reducing the disease incidence than T₂, the C:B ratio was higher (1:9.1) in respect of T₂ than T₃, which gave a C:B ratio of only 1:3.9. Hence, seed treatment with T. viride at 4g/kg + soil application of T. viride at 5kg/ha is a cost effective, eco-friendly management strategy for fenugreek root rot.     

Effects of D-D, Telone or dazomet applied to potato ridges in spring on potato cyst-nematode, Heterodera rostochiensis, in sandy loam and silt loam soils

Large amounts of dazomet (329, 439 kg/ha) applied to potato ridge soil in spring, before potatoes were planted, controlled potato cyst-nematode (Heterodera rostochiensis) in sandy loam and silt loam more effectively than large amounts of D-D (359, 448 kg/ha). In heavily infested sandy loam, 329 kg dazomet/ha or 857 kg methyl bromide/ha applied in spring 1969 or 439 kg dazomet/ha applied in autumn 1968, greatly decreased the number of larvae able to invade potato roots, so Majestic potatoes grew and yielded well without increasing the number of nematodes left in the soil after harvest. Large amounts of D-D or Telone applied to the topsoil in autumn or to the ridges in spring were less effective in controlling potato cyst-nematode or increasing potato yields. Applied in spring 1969 to silt loam ridges, 439 kg dazomet/ha had more effect than 448 kg D-D/ha on potato cyst-nematode and on the increase in yield of Majestic potato. The yield of Maris Piper potatoes (resistant to H. rostochiensis pathotype A) in infested silt loam was increased greatly by D-D, as much by 112 as by 224 or 448 kg/ha.     

Chemical control of stem nematode, Ditylenchus dipsaci, in field beans (Vicia faba)

‘Giant race’ stem nematode (Ditylenchus dipsaci) was well controlled in spring beans (Vicia faba) by up to 5 kg aldicarb or carbofuran ha^-1 applied to the seed furrows at sowing. Carbofuran was rather more effective in the clay loam soil used than was aldicarb. The best treatments almost eliminated injury to the stems and nematode infestation in the harvested seed. Similarly applied, oxamyl and fenamiphos were less effective and phorate, dimethoate and disulfoton were ineffective. Applying part of the dosage of an effective nematicide to the seed furrows and part along the plant rows mid-season was no more effective and was sometimes less effective than applying the whole dose to the seed furrows. Treating the plant rows mid-season with aldicarb or phoxim sometimes enhanced control but thiabendazole applied thus did not. Seed furrow applications of aldicarb or carbofuran were much less effective in controlling the nematodes in winter beans and seed dressings were less effective than seed furrow treatments. In one experiment, in plots in which aldicarb or oxamyl had been applied to the seed furrows, phoxim or thiabendazole applied over the rows of plants, enhanced nematode control. In two other experiments, thiabendazole was ineffective when applied in this way or when applied as a combined soil and plant treatment.     

Biological Control of Take-all Disease of Wheat Caused by Gaeumannomyces graminis var. tritici Under Field Conditions Using a Phialophora sp.

A Phialophora sp. (isolate I-52), originally isolated from soil in a wheat field exhibiting suppression of take-all disease caused by Gaeumannomyces graminis var. tritici , was tested under field conditions for its ability to suppress this disease in winter and spring wheat. I-52 was grown on a variety of autoclaved organic substrates, including oat, millet and canola seed. All of these gave significant disease control when added to the seed furrow with inoculum of the take-all fungus. W hole seed of I-52 substrate was as effective as particles < 0.5 mm in diameter. Placing I-52 in powdered form directly on to wheat seed was ineffective in controlling take-all. Rates as low as 2 g of I-52/3.3 m of row added with the seed provided some control of take-all, and nearly complete control in winter wheat was obtained using 15 g/3.3 m. The winter wheat host cultivar did not influence the degree of control of take-all by I-52.     

Treating potato ridges in spring with aldicarb, D-D or dazomet to control potato cyst-nematode, Heterodera rostochiensis, in sandy clay and peat loam soils

Applied to potato ridge soil in spring, before potatoes were planted, small amounts of aldicarb (10-3 kg/ha or less) controlled potato cyst-nematodes (Heterodera rostochiensis Woll.) better than large amounts of dazomet (110–466 kg/ha) or D-D (102–439 kg/ha). Applied in spring 1968 and 1969 to heavily infested sandy clay soil 466 kg dazomet/ha allowed Majestic potatoes to grow and yield well in both years without increasing the number of nematodes in the soil after harvest, but in peaty loam dazomet was toxic to potato plants and, when applied in autumn, killed fewer nematodes. D-D in potato ridges in spring controlled nematodes less well than dazomet or aldicarb, but 896 kg D-D/ha injected in sandy clay soil in autumn increased potato yield the following year without increasing the number of nematodes after harvest.     

The Effects of Seasonal Flooding on Seed Availability for Spring Migrating Waterfowl

Abstract: We hypothesized the seed biomass available to migrating waterfowl would be higher in spring- versus fall-flooded wetlands. To test this hypothesis we conducted an experiment using 5 pairs of wetland impoundments in northern Missouri, USA (2000-2002). We strategically assigned one impoundment of each pair to either a fall or spring treatment group. We estimated seed biomass in fall and in spring by clipping seed heads and collecting soil cores at 20 random locations within each impoundment. We placed exclosures near each fall sample site in spring-flooded impoundments to estimate seed loss from granivorous birds and rodents. Despite similar biomass in fall between treatments (P = 0.64), overwinter seed loss was greater in fall-flooded (79%; 1,324 ± 195 kg/ha) than in spring-flooded (31%; 653 6 130 kg/ha) impoundments (P = 0.009). Considering barnyard grass or millet (Echinochloa spp.) only, seed loss was higher in fall-flooded than in spring-flooded impoundments (P = 0.05). Spring biomass estimates were similar inside versus outside exclosures (P = 0.63) indicating loss to granivorous birds and rodents was limited. Our results suggest that fall flooding reduces seed availability for spring migrating waterfowl. We recommend spring flooding be used in areas where impoundment water levels can be manipulated to increase seed availability for spring migrating waterfowl.     

Soil conditions and the take-all disease of wheat; control of the disease under continuous cultivation of a spring-sown cereal

In a field experiment on the control of take-all at the Woburn Experimental Station, winter wheat was followed by two consecutive crops of spring-sown barley. Samples of the barley crop were taken from the forty-eight plots of the experiment in 1945 and 1946, for estimation of root Disease Rating, and grain yields were also recorded. A comparison of six autumn treatments of the stubble has shown that treatments affecting the available nitrogen content of the soil exercised a predominant effect upon incidence of take-all in the following crop. Two effects of nitrogen applied in autumn have been distinguished: (1) an immediate effect, in assisting survival of Ophiobolus graminis in infected root and stubble residues; (2) a deferred effect, in promoting disease escape of the following crop. The ploughing in of straw in autumn was found to increase the incidence of take-all, presumably because the adverse deferred effect of decomposing straw in locking up available nitrogen and withholding it from the following crop. outweighed its beneficial immediate effect in helping to starve out O. graminis , by depriving the fungus of nitrogen. The autumn growth of undersown trefoil ( Medicago lupulina ) on the stubble land seenled to be entirely beneficial; active growth of the legume appeared to assist in starving out O. graminis , and nitrogen was released by decomposition of the trefoil in the soil after spring ploughing in time to benefit the barley crop immediately following.     

The interaction of protectants with EPTC on field bean, and tri-allate on wheat

Protectants (antidotes) were tested for their potential to protect field beans (Vicia faba L.) from EPTC damage, or wheat (Triticum aestivum L.) from triallate damage. For both crops there was considerable variation in the degree of protection shown from similar treatments in different experiments. For field bean, a seed treatment of 1,8-naphthalic anhydride (NA) at 5 mg/g seed gave some protection from EPTC applied pre-planting at 4–8 kg a.i./ha but not in all experiments. NA also caused marked chlorosis of the foliage. N, N-diallyl-2, 2-dichloroacetamide (R25788) at 20 mg/g seed severely damaged field bean in the absence of herbicide but 5 mg/g gave comparable protection from EPTC to that given by NA and did not cause chlorosis. Mixing R25788 with EPTC in the spray tank gave reduced protection. In a single experiment R4115 (chemistry undisclosed) gave some protection against EPTC damage. For wheat, a seed treatment of 5–20 mg/g NA sometimes countered damage from tri-allate applied pre-planting at 1 kg a.i./ha but not generally from higher doses. R25788 sometimes protected from weight loss due to tri-allate at 1 kg a.i./ha but not from damage symptoms, whereas R4115 at 20 mg/g seed alleviated these symptoms but did not prevent weight loss. R25788 at 4 kg a.i./ha mixed in the spray tank with the herbicide partially reduced weight loss and damage symptoms from a dose of 2 kg a.i./ha. Some treatments of R29148 gave complete protection from tri-allate at 1 kg a.i./ha. The results are discussed in the context of the full data from the two series of experiments.     

Experiments on soil drenching with fungicides against take-all in wheat

In short term pot experiments benomyl, iprodione and KWG 0599 applied as soil drenches in several types of soil significantly suppressed take-all symptoms from inoculum placed just below wheat seeds planted 1×5 cm deep, and in sand but not other soils when seeds were 5 cm deep. Benomyl was, however, effective against inoculum below seed planted 5 cm deep in a loam-sand mixture when the drench contained an alcohol ethoxylate surfactant. Computer simulations of fungicide distributions in the soils correlated well with disease control observations. In long term outdoor pot experiments two drenches with benomyl (without surfactant) controlled disease significantly for at least 3 months against inoculum placed 15 cm deep. The significance of these results for the practical control of take-all by fungicides is discussed.     

Experiments with fungicides to control Aphanomyces cochlioides in sugar beet

Aphanomyces cochlioides attacking sugar-beet seedlings was controlled by fenaminosulf applied as seed treatment or to the seed furrow at sowing. In the absence of blackleg caused by A. cochlioides, fenaminosulf seed treatment at 0–75 % (of seed weight) and soil applications decreased seedling emergence, and soil applications of more than 2-2 kg a.i./ha significantly depressed sugar yield. Controlling moderate attacks of seedling blackleg caused by A. cochlioides did not increase yield. Dichlone, benomyl and maneb applied as seed or soil treatments, captafol seed treatment, and quintozene and thiram soil treatments did not control A. cochlioides.     

Control of Ditylenchus dipsaci in Infected Garlic Seed Cloves by Nonfumigant Nematicides

Different rates of granular formulations ofaldicarb, carbofuran, ethoprop, fensulfothion, and phenamiphos were applied directly onto garlic seed cloves in the seed furrow in sandy clay loam, clay loam, and loam soils at planting to assess efficacy for control of Ditylenchus dipsaci in infected seed cloves. All treatments were compared to hotwater-formalin clove dip disinfection treatment and to nontreated infected controls. Aldicarb and phenamiphos at 2.52 and 5.04 kg a.i./ ha, but not at lower rates, effectively suppressed infection by D. dipsaci and increased yields. Although both nematicides slightly slowed the rate of plant emergence, normal stands were established. Trace levels of infection occurred in all treatments, including the hotwater-formalin dip. Carbofuran at 5.04 kg a.i./ha controlled the nematode but was phytotoxic. Ethoprop was phytotoxic. Fensulfothion did not control D. dipsaci even at the highest application rate, 8.90 kg a.i./ha. Single and multiple applications of oxamyl at 1.12-8.96 kg a.i./ha, applied as a surface spray or in furrow irrigation water, slowed the early progression of disease symptoms but failed to provide season-long nematode control.     

Some effects of differently-acting nematicides on the cereal cyst-nematode (Heterodera avenae) and on the appearance of ''scorch'' in spring wheat on light loamy sand

In fungitoxicity tests against Phytophthora cinnamomi on Chamaecyparis lawsoniana cv. Ellwoodii, a drench of furalaxyl (1000 mg a.i./l) applied to the compost in which 1-yr-old plants were growing, 1 wk before they were inoculated with 650 000 zoospores, controlled disease for at least 12 months. With an inoculum dose of 650 zoospores/plant, furalaxyl at 500 mg a.i./l controlled disease even when inoculation was 12 wk after fungicide treatment. Aluminium tris (ethyl phosphonate) (2000 mg a.i./l) applied as a drench 1 wk before inoculation with 650 000 zoospores/plant did not prevent root infection but delayed foliar symptoms for 9 months: the same treatment, using etridiazole (500 mg a.i./l) only slightly reduced disease incidence. When applied as a single drench 2 days before inoculation, prothiocarb (2000 mg a.i./l) and cuprammonium compounds (200 mg a.i./l) were much less effective than furalaxyl (1200 mg a.i./l), sodium ethyl phosphonate (1500 mg a.i./l), aluminium tris (ethyl phosphonate) (1500 mg a.i./l) or etridiazole (500 mg a.i./l). However, a drench of furalaxyl at 1000 mg a.i./l, aluminium tris (ethyl phosphonate) at 2000 mg a.i./l or etridiazole at 500 mg'a.i./l did not eradicate P. cinnamomi from compost containing infected root debris. Pre-planting drenching of the compost was ineffective. All fungicide treatments were non-phototoxic to 1-yr-old C. lawsoniana cv. Ellwoodii. These results are of special relevance to the control of P. cinnamomi on container-grown woody ornamentals.     

Comparison of natural and artificial epidemics of take-all in sequences of winter wheat crops

Winter wheat was grown for six successive years (Expt 1) and for three successive years (Expt 2) in field experiments on different soil types. Artificial inoculum of the take-all fungus (Gaeumannomyces graminis var. tritici cultured on autoclaved oat grains) was incorporated in the soil of some of the plots just before, or at, sowing of the first winter wheat crop. Expt 1 tested the incorporation of similar amounts of inoculum (212 kg ha^-1) at different depths. Expt 2 tested different amounts of inoculum at the same, shallow depth. Early sowing (September), late sowing (October) and spring inoculation were additional treatments, applied to the first crop only, in Expt 2. Seasonal factors apart, the disease outcome in the first year after inoculation depended on amounts and placement of applied inoculum, as well as date of sowing. Deeper inoculum resulted in less disease (Expt 1). Severe take-all was produced in Expt 2 by incorporating inoculum shallowly in sufficient quantities (400 kg ha^-1 or more). Less inoculum (200 kg ha^-1) generated less disease, especially in earlier-sown plots. Differences in disease amongst inoculum treatments were greatest in the first year and diminished subsequently, particularly where sowing had been early in the first year. In Expt 1, where first crops exposed to artificial inoculum developed moderate-to-severe disease, disease in subsequent second and/or third crops was less. In the fourth crop a second peak of disease occurred, coinciding with a first peak in sequences without added inoculum. Take-all decline (TAD) appeared to be expressed in all sequences thereafter. In Expt 2 in sequences without added inoculum, TAD occurred after a peak of disease in the second crop. Where 400 kg ha^-1 or more of inoculum were added, disease was severe in the first year and decreased progressively in successive years. Disease was less patchy in plots that received artificial inoculum. However, it remains uncertain mat severe disease caused by artificial inoculation achieved an early onset of true TAD. The infectivity of the top 12 cm of soil in the first 3 yr of Expt 1, determined by bioassay, depended on the depth of added inoculum and amount of disease in subsequent crops. However, at the time of the naturally occurring peak of disease severity (in either inoculated or non-inoculated plots) it did not predict either disease or TAD. Differences and similarities amongst epidemics developing naturally and those developing from different amounts and placement of applied inoculum have been revealed. The epidemiological implications of adding inoculum and the potential value of artificially-created epidemics of take-all in field trials are discussed.     

Prospects for fungicidal control of take-all of wheat

A range of fungicides and herbicides was tested against Gaeumannomyces graminis (causal agent of take-all) on agar plates, and on wheat seedlings in pots and in liquid culture. Benomyl, the standard in all tests, was consistently most effective: like iprodione, nuarimol and KWG 0599 , it diminished infection from inoculum placed just below the seeds more effectively when applied as a drench than as a soil-mix. Benomyl as a soil-mix was most effective in soils with least organic matter. Some compounds toxic to the pathogen on agar plates and in plants grown in liquid culture were ineffective as soil treatments. The practical limitations of soil treatment with conventional fungicides and application methods are discussed.     

Efficacy of Oxamyl Against Heterodera schachtii on Cabbage

The efficacy of oxamyl in controlling Heterodera schachtii on cabbage was determined by applying various contbinations of soil drenches at 6.7 kg (a.i.)/ha and foliar sprays at 0.04 kg (a.i.)/100 liters of water to cabbage seedlings. Pretransplant drenches provided some control of H. schachtii over a 13-week period. A single foliar spray of oxamyl 1 week before transplanting apparently prevented penetration of H. schachtii larvae; post-transplant sprays were relatively ineffective. A pretransplant or transplant drench combined with a foliar application 2 weeks after transplanting provided the most effective control. The effectiveness of drenches plus post-transplant sprays is probably due to the spray augmenting the action of the drench in inhibiting the development of larvae after penelration.