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.     

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.     

A Simulation Model of Heterodera schachtii Infecting Beta vulgaris

A simulation model of a single sugarbeet, Beta vulgaris L., plant infected by the sugarbeet cyst nematode, Heterodera schachtii Schmidt, was developed using published information. The model is an interactive computer simulation programmed in FORTRAN. Given initial population densities of the nematode at planting, the model simulates nematode population dynamics and the growth of plant tap and fibrous roots. The driving variable for nematode development and plant growth is temperature.     

The Interrelationship of Heterodera schachtii and Ditylenchus dipsaci on Sugarbeet

Heterodera schachtii significantly (P = 0.05) reduced sugarbeet root growth below that of uninoculated controls at 20, 24, and 28 C, and Ditylenchus dipsaci significantly (P = 0.05) reduced root growth below that of uninoculated controls at 16, 20, 24, and 28 C. A combination of H. schachtii and D. dipsaci significantly (P = 0.05) reduced root growth below that of single inoculations of H. schachtii at all temperatures and D. dipsaci at 20, 24, and 28 C. Single inoculations of H. schachtii and D. dipsaci significantly (P = 0.05) reduced top growth of sugarbeet below that of uninoculated controls at 20, 24, and 28 C, and 16, 20, 24, and 28 C, respectively. A combination of the two nematodes significantly (P = 0.05) reduced top growth below that of single inoculations of H. schachtii at all temperatures. However, a combination of the two nematodes failed to significantly (P = 0.05) reduce top growth below that of single inoculations of D. dipsaci at any temperature. Inoculations of either H. schachtii or D. dipsaci did not affect penetration of the other nematode, and D. dipsaci did not affect development and reproduction of H. schachtii. D. dipsaci did not reproduce on sugarbeet.     

Improved Methods of Hatching Heterodera schachtii Larvae for Screening Chemicals

The rate of hatching of Heterodera schachtii larvae was greatly increased by placing cysts in sieves enclosed by small disposable cups. An apparatus that permitted rapid storage of second-stage larvae at 10 C prolonged the viability of the larvae.     

Influence of Meloidogyne hapla Chitwood, 1949 on Development and Establishment of Heterodera schachtii Schmidt, 1871 on Beta vulgaris L

Influence of Meloidogyne hapla on estahlishnrent and maturity of Heterodera schachtii in sugarbeet was studied. Results indicated that when the majority of M. hapla were in second, third, or fourth larval stages within plants prior to H. schachtii inoculation, growth and development of the latter was retarded. However, when M. hapla reached the young female stage prior to inoculation of H. schachtii, establishment and development of the latter was greatly enhanced. As M. hapla reached maturity before and after egg production prior to H. schachtii inoculation, establishment and growth of the latter was progressively decreased. In each instance, M. hapla developed independently and matured at the same rate as in plants inoculated with only M. hapla. Usually ratios of total soluble carbohydrates to reducing carbohydrates were lower, but not significantly different, in plants receiving both nematodes as compared to other treatments.     

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.     

Susceptibility of plant selections to Heterodera schachtii and a race of H. trifolii parasitic on Sugarbeet in The Netherlands

Similar host ranges were found for Heterodera schachtii and a race of H. trifolii parasitic on sugarbeet in The Netherlands. Twenty-nine of 41 plant accessions evaluated were susceptible to H. trifolii. Five breeding lines of the interspecific hybrid Beta vulgaris-B. procumbens which are resistant to H. schachtii were highly susceptible to H. trifolii. An accession of B. maritima with partial resistance to H. schachtii was resistant to H. trifolii.     

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.     

Self-interactions of Meloidogyne hapla and of Heterodera schachtii on Beta Vulgaris

Double inoculations of sugar beet with larvae of Meloidogyne hapla resulted in a higher galling incidence in only one treatment than did a single inoculation using the same number of larvae. Double inoculations with larvae of Heterodera schachtii, however, resulted in three- to five-fold more cysts in most cases than did single inoculations using the same number of larvae. In general, plants died more quickly after double inoculations than after single inoculations of the same total number of either nematode. Ratios of total soluble carbohydrates to reducing carbohydrates were lower in multiple inoculated treatments than in other treatments. Plants infected with M. hapla had lower quantities of B, K, and P in leaf tissue than noninoculated plants, but no differences were correlated with type of inoculation. Plants inoculated with H. schachtii had lower quantities of B, K, and Mg than noninoculated plants. Also, quantities of Mn, Cu, and Zn were much lower in plants inoculated twice with H. schachtii larvae than in plants inoculated with the same total number of larvae in a single dose.     

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 Heterodera schachtii Population Densities to Sugarbeet Yields

Sugarbeet yields were contpared with field populations of Heterodera schachtii Schmidt. The correlation between sugarbeet yields and viable larvae/g of soil was negative and high, but that between sugarbeet yields and viable cysts/g of soil was lower. Sugarbeet yields were also compared with H. schachtii populations by years of rotation with a nonhost crop. The coefficients of correlation (r) between yield and viable larvae/g of soil were negative and high: 0 yr of rotation, -0.935; 1 yr, -0.922; 2 yr, -0.954; 3 yr, -0.935; and combined years, -0.965, with 95% confidence limits of -0.91 to -0.98 for combined years. The comparable correlation coefficients between yield and "viable cysts"/g of soil were negative and lower: 0 yr of rotation, -0.151; 1 yr, -0.022; 2 yr, -0.490; 3 yr, -0.456; and combined years, -0.586, with 95% confidence limits of -0.22 to -0.80 for the combined years.     

Interrelationship of Heterodera schachtii and Meloidogyne hapla on Tomato

Invasion of tomato (Lycopersicon esculentum L.) roots by combined and sequential inoculations of Meloidogyne hapla and a tomato population of Heterodera schachtii was affected more by soil temperature than by nematode competition. Maximum invasion of tomato roots, by M. hapla and H. schachtii occurred at 30 and 26 C, respectively. Female development and nematode reproduction (eggs per plant) of M. hapla was adversely affected by H. schachtii in combined inoculations of the two nematode species. Inhibition of M. hapla development and reproduction on tomato roots from combined nematode inoculations was more pronounced as soil temperature was increased over a range of 18-30 C and with prior inoculation of tomato with H. schachtii. M. hapla minimally affected H. schachtii female development, but there was significant reduction in the buildup of H. schachtii when M. hapla inoculation preceded that of H. schachtii by 20 days.     

The Relationship Between Population Density of Heterodera schachtii,Soil Temperature,and Sugarbeet Yields

In two glasshouse experiments, relations between sugarbeet root dry weight (y, expressed as a percentage of the maximum dry root weight), and preplanting populations of Heterodera schachtii (P_i) were described by the equation y = 100(Z)^P_i-T, in which Z = a constant slightly smaller than 1, and T = the tolerance limit (the value of P_i below which damage was not measureable). T varied with temperature; it was 65 eggs/100 g soil at 23 and 27 C and 430 eggs/100 g soil at 19 C. At 15 and 31 C there was no loss of root dry weight up to the maximum preplanting populations tested. In a field experiment in the Imperial Valley the relation between root yield (y) and P_i was y = 100 (0.99886)^P_i - 100, and the tolerance limit was 100 eggs/100 g soil.     

Comparative Morphometrics of Eggs and Second-Stage Juveniles of Heterodera schachtii and a Race of H. trifolii Parasitic on Sugarbeet in The Netherlands

Measurements of second-stage juveniles of Heterodera schachtii from California and The Netherlands and a race of H. trifolii from The Netherlands were obtained and compared to determine if these populations can be differentiated by morphometrics. Juvenile lengths of 10 specimens from each of 10 cysts of each population were measured. Dimensions of tail regions of 20 juveniles from individual cysts of H. schachtii (California) and a like number of juveniles of H. trifolii (The Netherlands) were also obtained. The mean lengths of juveniles of H. schachtii from California and The Netherlands were not significantly different, but similar measurements of H. schachtii and H. trifolii were different (P = 0.05). Mean dimensions of tail lengths, tail widths, tail hyaline lengths, and tail length/tail width were significantly greater for H. trifolii than for H. schachtii. Also, dimensions of eggs of H. trifolii were significantly greater than dimensions of H. schachtii eggs. The investigations established that H. schachtii can be readily differentiated from H. trifolii by morphometrics of eggs and juveniles, Minimum sample sizes required for specified confidence intervals for each criterion measured are provided.     

Parasitism of Beta vulgaris by Meloidogyne hapla and Heterodera schachtii Alone and in Combination

Interrelationships of Meloidogyne hapla and Heterodera schachtii in combinations of several population levels and different inoculation periods were studied. Results indicated suppression of gall development of M. hapla in any treatment in which inoculations of H. schachtii preceded those of M. hapla by 10 days. This interrelationship was characterized by amensalism with M. hapla serving as an amensat and H. schachtii serving as an inhibitor. Conversely, when inoculations of M. hapla preceded H. schachtii inoculations by 10 days, there were increases in cyst development. This relationship was characterized by commensalism with H. schachtii serving as a commensal. In both interactions, the preinvading parasites acted independently and established populations equal to treatments receiving either parasite alone. When both nematodes were inoculated simultaneously, there were no effects on populations of either. Relationships of this nature were characterized by neutralism. Ratios of total soluble/reducing carbohydrates were lower in treatments when M. hapla inoculations preceded those of H. schachtii. Plants inoculated with both nematodes died earlier than those inoculated with either parasite alone. High concentrations of Al and Fe occurred in treatments wherein M. hapla or H. schachtii inoculations preceded each other by 10 days. Generally, noninoculated control plants exhibited higher concentrations of K, P, Mg, and B than other treatments.     

Host Suitability and Susceptibility of Glycine max cv. Bedford to Race 1 of Heterodera glycines

Populations of Heterodera glycines identifiable as race 1 reproduced on the race 1 resistant ''Bedford'' soybean. A Beaufort County, North Carolina, population had an index of parasitism of 112% on Bedford in greenhouse tests. Indices of parasitism for this population on race 1 resistant cultivars Pickett 71, Centennial, and Forrest were less than 10%. The Beaufort County population had significantly greater reproduction on Bedford in microplots than did populations of race 3 or race 4. In field tests, a race 1 population suppressed yields of Bedford but not yields of Centennial. Based on these data, Bedford is no longer recommended in North Carolina as a race 1 resistant cultivar.     

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.     

Influence of Nonhosts, Crucifers, and Fungal Parasites on Field Populations of Heterodera schachtii

Heterodera schaehtii egg number decline under nonhosts was surveyed for 3-4 years at soil depths of 0-30 cm and 30-60 cm in three fields in the Imperial Valley, California. In the two fields continously cropped to alfalfa, annual decline rates were 49 and 63%, respectively, and did not differ (P = 0.05) between depths. In the third field, cropped to annual nonhosts and fallowed, decline rates of 56 and 80% at 0-30-cm and 30-60-cm depths, respectively, were significantly different (P = 0.05). Egg hatch is the major cause of decline. Soil moisture in relation to type of cropping sequence apparently influenced egg hatch and activity of fungal parasites. An interaction matrix is used to assess the importance of biological, environmental, and management factors affecting decline of H. schachtii egg numbers. The required rotation length to non-hosts for various egg densities can be predicted. In coastal California, inclusion of a winter crucifer crop in the rotation increased H. schachtii egg density up to threefold.     

A Comparison of the Hatching of Juveniles from Cysts of Heterodera schachtii and H. trifolii

The effects of root diffusates of selected plants within the families Chenopodiaceae and Cruciferae and the hatching agent zinc chloride were tested for their effects on hatching and emergence of juveniles from cysts of Heterodera schachtii and a race of H. trifolii parasitic on Chenopodaceae and Cruciferae in The Netherlands. Although all diffusates strongly stimulated hatching of juveniles of H. schachtii, their effects on H. trifolii were less evident.