In-Vitro and In-Vivo Effects of Aldicarb on Survival and Development of Heterodera schachtii

Aqueous solutions of 5-500 μg/ml aldicarb inhibited hatching of Heterodera schachtii. Addition of hatching agents, zinc chloride, or sugarbeet root diffusate, to the aldicarb solutions did not decrease the inhibition of hatching. When cysts were removed from the aldicarb solufions and then treated for 4 wk in sugarbeet root diffusate, larvae hatched and emerged. Treatments of newly hatched larvae of H. schachtii with 5-100 μg/ml aldicarb depressed later development of larvae on sugarbeet (Beta vulgaris). Similar treatments with aldicarb sulfoxide had less effect on larval development, and aldicarb sulfone had no effect. Numbers of treated larvae that survived and developed were inversely proportional to concentration (0.1-5.0 μg/ml) and duration (0-14 days) of aldicarb treatments. Development of H. schachtii on sugarbeet grown in aldicarb-treated soil was inversely proportional to the concentration of aldicarb in the tested range of 0.75 - 3.0 μg aldicarb/g of soil. Transfer of nematode-infected plants to soil with aldicarb retarded nematode development, whereas transfer of plants first grownin treated soil to nematode-infested soil only slightly suppressed nematode development. Development of H. schachtii was inhibited in slices of storage roots of table beet (B. vulgaris), sugarbeet and turnip, (Brassica rapa), that had grown in soil treated with aldicarb.     

Residues of Aldicarb and its Oxides in Beta vulgaris L. and Systemic Control of Heterodera schachtii

Altlicarb residues in foliage of Beta vulgaris L. 21 days after transplanting to soil treated with 1-5 μg aldicarb/g soil were proportional to residues in storage roots, but 20 times as great. Initial concentrations of residues in roots 21 days after treatment were proportional to applied rates but declined by 56% when roots were stored 25 days at 24 C. Mean respective concentrations of aldicarb, aldicarb sulfoxide, and aldicarb sulfone were 8.7, 81.6, and 9.8% of the total residues. In separate tests, equivalent concentrations of toxic carbamates in roots resulted in similar levels of control of Heterodera schachtii. Systemic levels that completely suppressed development of females and males on sectioned roots were respectively 0.35 and 0.8 μg/g of root tissue.     

Development of Heterodera schachtii on Large Rooted Crop Plants and the Significance of Root Debris as Substratum for Increasing Field Infestations

Heterodera schachtii developed to maturity and reproduced on the lateral roots of defoliated sugarbeet which were buried to a depth of 2.5 cm in sterilized soil and inoculated with cysts. Nematodes did not develop on detached lateral roots or on roots of young defoliated beets which did not have a large tap root. The storage roots of large rooted plants were sliced, placed in small jars, inoculated with cysts, covered with moist granulated agar or soil and incubated at 24°C 12-62 days. The sugarbeet nematode developed in root slices of sugarbeet, red table beet, icicle and globe radish, turnip and rutabaga. Only a few males developed on slices of potato tubers. Neither males nor females developed on root slices of carrot, salsify or parsnip. H. schachtii also developed on the cut surfaces of growing sugarbeet and radish.     

The Relationship of Plant Age,Soil Temperature,and Population Density of Heterodera schachtii on the Growth of Sugarbeet

There were direct relationships between inoculum density of Heterodera schachtii Schm. (nematode population density), initial soil temperature, the growth of sugarbeets in the greenhouse under controlled temperatures, and nematode populations. Heterodera schachtii was least pathogenic on plants inoculated at 6 wk of age and most pathogenic on plants grown from inoculated germinated seed (0 wk of age). In the field, H. schachtii was least pathogenic on sugarbeets grown at an initial soil temperature of 6 C and most pathogenic on those grown at an initial soil temperature of 24 C. The growth period for sugarbeets at the different soil temperatures was determined by heat units; since penetration of sugarbeet roots by H. schachtii larvae is accelerated at soil temperatures above 10 C, each hour-degree ahove 10 C was counted as one effective heat unit (HU). Using this guideline it was determined that root weight depressions in the greenhouse, for each degree-unit population (HU-UP) where unit population = one larvae/g soil, were 0.052, 0.09, 0.12, and 0.17 mg at initial soil temperatures of 6, 12, 18, and 24 C, respectively. Root weight depressions were 0.28, 0.23, 0.15, and 0.086 mg when plants were inoculated at 0, 2, 4, and 6 wk of age.     

Behavioral Responses of Heterodera rostochiensis Larvae to Aldicarb and its Sulfoxide and Sulfone

Temik® aldicarb pesticide [2-Methyl-2-(methylthio) propionaldehyde-O-(methylcarbamoyl) oxime] is an effective contact and systemic compound against a wide variety of agricultural pests. Its metabolism in soils may lead to aldicarb sulfoxide and aldicarb sulfone which are both toxicologically important. The comparative effects of these compounds on body activity and stylet movement of second-stage larvae of the potato cyst nematode, Heterodera rostochiensis, were investigated. Temik aldicarb was the most effective contact toxicant, rapidly inhibiting body activity and stimulating abnormal stylet movement. A 24-hr post-nematicide water treatment allowed effective recovery of body vigor and cessation of abnormal stylet movement of the larvae treated with Temik aldicarb at low concentrations, and with aldicarb sulfoxide and aldicarb sulfone at all the dosage levels used. Larvae treated with 10 ppm Temik aldicarb remained paralyzed, the toxic effect being apparently irreversible. Control of Heterodera rostochiensis by direct contact toxicity may not be effective in soil since Temik degrades to compounds having reversible toxic effect.     

Effects of Aldicarb on the Behavior of Heterodera schachtii and Meloidogyne javanica

The toxic effects of sublethal concentrations ofaldicarb were studied on eggs and second-stage larvae and males of Heterodera schachtii and second-stage larvae only of Meloidogyne javanica in a quartz sand substrate. Aldicarb was more toxic to eggs of H. schachtii than to those of M. javanica. Complete suppression of hatching occurred between 0.48 and 4.8 μg/ml aldicarb for H. schachtii whereas 100% inhibition of hatch of M. javanica occurred between 4.8 and 48.0 μg/ml. M. javanica hatch was stimulated at 0.48 μg/ml aldicarb. Migration of second-stage larvae of H. schachtii and M. javanica in sand columns was inhibited under continuous exposure to 1 μg/ml aldicarb. Infection of sugarbeet and tomato seedlings by larvae was inhibited at 1 μg/ml. H. schachtii males failed to migrate toward nubile females at 0.01 μg/ml aldicarb. This was partially confirmed in a field study in which adding aldicarb to soil resulted in fewer females being fertilized.     

Effects of Selected Nematicides on Hatching of Heterodera schachtii

Aldicarb, carbofuran, fensulfothion, and phenamiphos were tested in concentrations of 1-100 μg/ml for their effects on hatching of Heterodera schachtii. Exposure of cysts to 1 μg aldicarb or carbofuran/ml stimulated hatch whereas phenamiphos and, to a lesser degree, fensulfothion inhibited hatch. Addition of aldicarb to sugarbeet root diffusate or 4 mM zinc chloride suppressed activities of these hatching agents. Transfer of cysts previously treated with aldicarb or carbofuran to zinc chloride or water rapidly initiated hatch which finally exceeded the hatch from cysts not treated with the nematicides.     

Effects of Cycloate on Development of Heterodera schachtii and Growth of Three Beta Species

Greenhouse tests were set up to evaluate the effects of the herbicide, cycloate (S-ethyl cydohexylethylthiocarbamate), oil development of Heterodera schachtii and growth of three Beta species. Cycloate added to infested soil enhanced cyst development/gm root on B. vulgaris and larvae/gm of root in B. patellaris and B. procumbens at 4, 16, and 16 μg(a.i.)/gm of soil, respectively. Total numbers of nematodes/individual root system decreased because of poor root growth of seedlings in cycloate-amended soil. Penetration and larval development through stage three did occur in the wild Beta species in any treatment. Thus, resistance of B. patellaris and B. pocumbens to development of H. schachtii was not altered by cycloate. Cycloate also retarded growth (P = 0.05) of the sugarbeet cultivars and B. patellaris at 4 μg(a.i.)/gm and B. procumbens at 16 μg(a.i.)/gm of soil. Higher concentrations of nematodes/gm root in plants growing in cycloate-amended soil may be attributed to factors such as fewer roots available for penetration, possible effects of cycloate on egg hatch, greater attraction of nematodes to roots, and increased susceptibility of roots to larval penetration. Suppression of seedling growth in cycloate-amended soil may be attributed in part to higher nematode density and in part to direct root damage from cycloate.     

Pathological Differences in Heterodera schachtii Populations

Five populations of Heterodera schachtii Schm. from Oregon, Idaho, and Utah did not differ significantly in seedling penetration and rate of emergence and virulence. Another Utah H. schachtii population (Utah 2), however, differed from these five populations in all of the above-mentioned characteristics. More H. schachtii larvae of the Utah 2 population than the other populations penetrated sugarbeet seedlings at 10, 15, 20, and 25 C. Root and top weights of sugarbeet plants were signiticantly less when roots were parasitized by the Utah 2 population than when they were parasitized by larvae of the other nematode populations under similar experimental conditions. Also, the period of larval emergence was shorter in the Utah 2 population than in any of the other H. schachtii populations.     

Effects of Aldicarb and Its Sulfoxide and Sulfone on the Biology of Tylenchulus semipenetrans

In laboratory testing, egg hatch of Tylenchulus semipenetrans was stimulated at concentrations of 1 and 10 μg/ml aldicarb solution and inhibited at 50 and 100 μg/ml. Aldicarb was more inhibitory to egg hatch than the aldicarb sulfoxide and the aldicarb sulfone. Inhibition of hatch at the high concentration was associated with delays in the molting processes, lack of larval movement within the egg, and delays in embryonic development. Nematode motility was reduced at 10, 50, and 100 μg/ml of aldicarb and aldicarb sulfoxide solution, and at 50 and 100 μg/ml aldicarb sulfone. Male development was retarded at 10 μg/nrl and almost completely inhibited at 50 and 100 μg/ml of the three chemicals. In greenhouse tests, female development antl reproduction on roots of citrus seedlings were suppressed by aldicarb at rates of 2.6 μg/ml and completely inhibited at 10.6 μg/ml of soil solution during a 50-day experimental period. Under field conditions, there was little systemic movement of aldicarb into roots located outside treated areas. Aldicarb reduced the nematode larvae and the female adult population in the second year after the second treatment. There were no differences in egg hatch and sex ratio of citrus nematodes between treated and nontreated roots.     

Population Dynamics of Heterodera schachtii on Tomato and Sugar Beet

Experiments showed that development of male and female Heterodera schachtii on tomato and sugarbeet are disproportionately influenced by the nematode inoculum level and root size, which together determine the density of invading larvae. Slight overcrowding favored development of males over females, whereas severe overcrowding equally affected development of males and females. Differential population changes of host-selected races on tested cultivars was attributable to selective development of male and female nematodes.     

Effects of Soil Moisture on Control of Heterodera schachtii with Aldicarb

Soil moisture and the nematode population density in aldicarb-treated soil influenced control of the sugarbeet nematode, Heterodera schachtii. Greater numbers of nematode larvae infected 14-day-old sugarbeet seedlings growing in aldicarb-treated soil at 20-30% than at 80-100% field capacity (F. C.), and plant growth was inversely related to nematode infection and the nematode population density. Compared with that of control plants, plant growth increase also was greater at 80-100% F. C. when the nematode population was above 1.8 larvae/gm soil. A nematode population of 1.8 larvae/gm soil did not significantly affect sugarbeet yields. Aldicarb gave less control when soil moisture levels dropped to 20 and 50% F. C. at nematode populations of 3.5 and 6.2 larvae/gm soil. More effective control was obtained wth soil moisture levels at or above 80% F. C. This difference was attributed to continued activity of the toxicant in the rhizosphere at the high moisture level.     

Accelerated Degradation of Aldicarb and Its Metabolites in Cotton Field Soils

The degradation of aldicarb, and the metabolites aldicarb sulfoxide and aldicarb sulfone, was evaluated in cotton field soils previously exposed to aldicarb. A loss of efficacy had been observed in two (LM and MS) of the three (CL) field soils as measured by R. reniformis population development and a lack of cotton yield response. Two soils were compared for the first test—one where aldicarb had been effective (CL) and the second where aldicarb had lost its efficacy (LM). The second test included all three soils: autoclaved, non-autoclaved and treated with aldicarb at 0.59 kg a.i./ha, or not treated with aldicarb. The degradation of aldicarb to aldicarb sulfoxide and then to aldicarb sulfone was measured using high-performance liquid chromatography (HPLC) in both tests. In test one, total degradation of aldicarb and its metabolites occurred within 12 days in the LM soil. Aldicarb sulfoxide and aldicarb sulfone were both present in the CL soil at the conclusion of the test at 42 days after aldicarb application. Autoclaving the LM and MS soils extended the persistence of the aldicarb metabolites as compared to the same soils not autoclaved. The rate of degradation was not changed when the CL natural soil was autoclaved. The accelerated degradation was due to more rapid degradation of aldicarb sulfoxide and appears to be biologically mediated.     

Suppression of Cyst Nematode by Natural Infestation of a Nematophagous Fungus

Penetration of cabbage roots by Heterodera schachtii was suppressed 50-77% in loamy sand naturally infested with the nematophagous fungus Hirsutella rhossiliensis. When Heterodera schachtii was incubated in the suppressive soil without plants for 2 days, 40-63% of the juveniles had Hirsutella rhossiliensis spores adhering to their cuticles. Of those with spores, 82-92% were infected. Infected nematodes were killed and filled with hyphae within 2-3 days. Addition of KCl to soil did not increase infection of Heterodera schachtii by Hirsutella rhossiliensis. The percentage of infection was lower when nematodes were touched to two spores and incubated in KCl solution than when nematodes naturally acquired two spores in soil.     

Relationship Between Heterodera schachtii,Meloidogyne hapla,and Nacobbus aberrans on Sugarbeet

Heterodera schachtii, Meloidogyne hapla, and Nacobbus aberrans either alone, or in various combinations with each other, can, when inoculated at a concentration of 12 second-stage juveniles/ cm³ of soil, cause a significant (P = 0.01) suppression of growth of sugarbeet (cv. Tasco AH14) seedlings. M. hapla and H. schachtii decreased growth of sugarbeet more than N. aberrans over a 60-day period. The adverse effect of N. aberrans on the final population/initial population (Pf/Pi) ratio for either M. hapla or H. schachtii was dependent on time, and was more accentuated on that of M. hapla than on that of H. schachtii. Neither M. hapla nor H. schachtii had an adverse effect on the Pf/ Pi ratio of N. aberrans. N. aberrans is considered to be less aggressive on sugarbeet than either H. schachtii or M. hapla. Sections of sugarbeet roots infected simultaneously with H. schachtii and N. aberrans showed scattered vascular elements between the N. aberrans syncytium located in the central part of the root and that of H. schachtii in the peripheral position.     

Chemical control of beet cyst-nematode, Heterodera schachtii, in some peaty loam soils

In peaty loam soils, aldicarb or oxamyl mixed with the top 15 cm of the soil in spring before sugar beet seeds were sown, minimised invasion of the roots by larvae of the beet cyst-nematode, Heterodera schachtii, so preventing injury to the seedlings, and greatly increased sugar yields in heavily infested soil. Small amounts of both compounds were often as effective as larger amounts. Nematode increase on sugar beet roots was slow. Aldicarb or oxamyl lessened nematode increase in four years out of five. Fumigating predetermined row positions with dichloropropene mixtures (D-D, Telone) or incorporating aldicarb or methomyl shallowly in soil, later occupied by the roots of sugar beet seedlings, did not control the nematode, although sugar yields were sometimes increased.     

Resistance of Trisomic and Diploid Hybrids of Beta vulgaris and B. procumbens to the Sugarbeet Nematode,Heterodera schachtiis Arnold

Trisomic and diploid hybrids of sugarbeet (Beta vulgaris L.) X wild beet (B. procumbens Chr. Sin.) inherited the gene for resistance to Heterodera schachtii Schm. from B. procumbens. The hybrids showed partial resistance to H. schachtii, manifested in failure of larvae to reach maturity. Although significantly greater numbers of female nematodes developed on plants inoculated with populations from the Netherlands or Italy than on plants inoculated with a population from the Salinas Valley, California. the totals for all populations on resistant plants were small. Greater numbers of males than females developed on root-slice cultures of resistant hyhrids when compared to a susceptible cultivar.     

The Effects of Hot Water Treatments on Survival of Heterodera schachtii

Cysts of Heterodera schachtii were treated in a water bath at constant temperatures ranging from 45 - 62.5 C for 1 sec to 28 hr. Treated and untreated cysts were incubated 8 weeks in sugarbeet root diffusate at 24 C to measure emergence of surviving larvae. Within the temperature range of 49 - 54 C, the minimum lethal temperature was proportional to the log time of treatment. No larvae emerged from cysts exposed 10 sec at 60 C. Although treatment of cysts for 8 hr at 45 C significantly reduced emergence, increasing the treatment period to 28 hr did not completely suppress emergence.     

Effect of Liquid Nutrient Culture,Vacuum Distillation and Dialysis on Hatching Activity of Sugar Beet Root Diffusate for Heterodera schachtii

Roots of sugar beets grown in liquid culture excrete substances that stimulate egg hatch and emergence of larvae from cysts of Heterodera schachtii. Their hatching effect is comparable to that of sugar beet root diffusate leached from soil-grown sugar beet plants. Consequently, liquid culture provides a way of obtaining H. schachtii hatch-stimulant free of contaminants from soil. Root diffusate, concentrated 50-fold or dried by vacuum distillation, retained hatching activity. The active principle of diffusate is dialyzable with a diffusion rate between those of inorganic salts and compounds with molecular weights greater than 15,000.     

Pathological Interaction of a Combination of Heterodera schachtii and Meloidogyne hapla on Tomato

Increased culturing of a tomato population of Heterodera schachtii (UT1C) on tomato for 480 days (eight inoculation periods of 60 days each) significantly increased virulence to ''Stone Improved'' tomato. A synergistic relationship existed between Meloidogyne hapla and H. schaehtii on tomato. A combination of H. schachtii (UTIC) and M. hapla significantly reduced tomato root weights by 65, 64, and 61% below root weights of untreated controls, and single inoculations of M. hapla and H. schachtii, respectively. This corresponded to root reductions of 42, 44, and 46% from a combination of H. schachtii (UT1B) and M. hapla. Antagonism existed between H. schachtii and M. hapla with regard to infection courts and feeding sites. The root-knot galling index dropped from 6.0 with a single inoculation of M. hapla to 4.3 and 3.3 with combined inoculations of M. hapla plus UT1B and M. hapla plus UTIC cyst nematode populations. The pathological virulence of H. schachtii to sugarbeet was not lost by extended culturing on tomato; there were no differences in penetration, maturation, and reproduction between sugarbeet populations continually cultured on sugarbeet and the population continually cultured on tomato.