Interrelationships of Meloidogyne arenaria and M. incognita on Tolerant Soybean

Reproduction of Meloidogyne arenaria race 2 was excellent on Centennial, Govan, and Kirby soybeans, the latter two of which have tolerance to this species. The M. incognita race 1 isolate reproduced poorly on Centennial, especially at the higher of two temperature regimes. Numbers of galls and egg masses of M. arenaria plus M. incognita in simultaneous equivalent infestations on Centennial did not differ from sequential infestations in which M. arenaria was added first and M. incognita was added to the same pots, 1,2, or 3 weeks later. However, at both 25 and 30 C, suppression of galls and egg masses occurred when inoculation of M. incognita preceded that of M. arenaria by 2 weeks. Generally, M. arenaria reproduced well at 25 or 30 C, whereas M. incognita reproduced better at 30 C. Kirby was tolerant to either nematode species at 25 and 30 C, but in combined infestations of M. arenaria and M. incognita there was evidence of synergistic growth suppression. Govan was tolerant of M. arenaria at 25 C but not at 30 C. Moreover, general plant growth was less vigorous for Govan at the higher temperature, whereas Centennial was much more vigorous at this temperature. Kirby grew equally well at both temperatures.     

Interactions Between Meloidogyne incognita and Pratylenchus brachyurus on Soybean

Interactions among Meloidogyne incognita, Pratylenchus brachyurus, and soybean genotype on plant growth and nematode reproduction were studied in a greenhouse. Coker 317 (susceptible to both nematodes) and Gordon (resistant to M. incognita, susceptible to P. brachyurus) were inoculated with increasing initial population densities (Pi) of both nematodes individually and combined. M. incognita and P. brachyurus individually usually suppressed shoot growth of both cultivars, but only root growth on Coker 317 was influenced by a M. incognita × P. brachyurus interaction. Reproduction of both nematodes, although dependent on Pi, was mutually suppressed on Coker 317. P. brachyurus reproduced better on Gordon than on Coker 317 but did not affect resistance to M. incognita. Root systems of Coker 317 were split and inoculated with M. incognita or P. brachyurus or both to determine the nature of the interaction. M. incognita suppressed reproduction of P. brachyurus either when coinhabiting a half-root system or infecting opposing half-root systems; however, P. brachyurus affected M. incognita only if both nematodes infected the same half-root system.     

Development of Meloidogyne arenaria on Peanut and Soybean under Two Temperature Cycles

Florunner peanut and three soybean cultivars, Centennial, Gasoy 17, and Wright, were inoculated with 48-hour age cohorts of Meloidogyne arenari race 1 second-stage juveniles and placed in a growth chamber set to simulate early season (low temperature) and midseason (high temperature) conditions. Percentages of the initial inoculum penetrating roots 4 and 8 days after inoculation were 2-3 times higher in soybean cultivars than in peanut; 25% on susceptible soybean and 9% on peanut. Penetration and early development of M. arenaria were greater in the higher temperature environment. Penetration percentages were expressed as a function of cumulative degree-days by regression models. Development of M. arenaria 10, 20, and 30 days after inoculation was more rapid on peanut than on soybean. The resistant soybean cultivar Wright had slower development rates than did the other two soybean cultivars. Nematode growth and development were dependent on temperature. In greenhouse experiments, production of eggs by M. arenaria was more than 10 times greater on peanut than on susceptible soybean. The reproductive factor for Wright soybean was less than one, but plant growth parameters indicated that this cultivar was intolerant of M. arenavia.     

Response of Soybean Cultivars to Nematicidal Treatments of Soil Infested with Meloidogyne incognita

A comparison of untreated and nematicide-treated soil for soybean production revealed that Meloidogyne incognita hastened crop maturity and reduced plant ht, seed wt, and yield. Reductions of yield varied from 32-90% depending on cultivar susceptibility. DBCP was more consistent in increasing crop performance than organo-phosphale or oxime carbamate nematicides. Greatest yield increases were produced by nematicidal treatment of soils planted to soybean cultivars with the lowest susceptibility.     

Penetration and Post-infectional Development and Reproduction of Meloidogyne arenaria Races 1 and 2 on Susceptible and Resistant Soybean Genotypes

Penetration, post-infectional development, reproduction, and fecundity of Meloidogyne arenaria races 1 and 2 were studied on susceptible (CNS), partially resistant (Jackson), and highly resistant (PI 200538 and PI 230977) soybean genotypes in the greenhouse. The ability to locate and invade roots was similar between races, but more juveniles penetrated roots of susceptible CNS than the resistant genotypes. At 10 days after inoculation, 56% and 99% to 100% of race 1 second-stage juveniles were vermiform or sexually undifferentiated in CNS and the resistant genotypes, respectively. In contrast, only 2%, 42%, 44%, and 62% of race 2 juveniles had not initiated development in CNS, Jackson, PI 200538, and PI 230977, respectively. By 20 days after inoculation, 88% to 100% of race 2 nematodes in roots of all genotypes were females, whereas only 25% and 1% of race 1 were females in CNS and the resistant genotypes, respectively. For all four genotypes, race 1 produce 85% to 96% fewer eggs per root system 45 days after inoculation than race 2. At 45 days after inoculation race 2 produced more eggs on CNS than the other genotypes.     

Pathogenicity and Reproduction of Hoplolaimus columbus and Meloidogyne incognita on 'Davis' Soybean

The effects of initial populations of Hoplolaimus columbus and Meloidogyne incognita on growth and yield of Davis soybean were determined for 1980 and 1981 in microplots and H. columbus in field tests in 1981. M. incognita suppressed yield in microplots both years and H. columbus in 1980. Maximum suppression of dry pod weight by M. incognita was 45% and by H. columbus 35%. The relationship of yield vs. nematode population at planting time was described by a declining exponential model. Maximum reproductive rates for M. incognita and H. columbus were 67.0 and 4.7, respectively, and were inversely proportional to initial population level. Nematode reproductive rates, survival ability, and feeding habits suggest species specific life strategies in the ecological community.     

Interaction between Meloidogyne incognita and Hoplolaimus columbus on Davis Soybean

Greenhouse and laboratory experiments were performed to determine if an interaction exists between Meloidogyne incognita and Hoplolaimus columbus on Davis soybean. Greenhouse tests were performed with three population levels of M. incognita and H. columbus (0, 1,500, 6,000/1.5-liter pot) separately and in all combinations. Dry root weight (DRT) declined nonlinearly and dry shoot weight (DST) declined linearly with respect to increasing initial populations of M. incognita and H. columbus. When the two nematode species were added to the soil together, the amount of DRT and DST suppression by one species was dependent on the initial level of the concomitant species. The final root population of M. incognita or H. columbus declined linearly with increasing initial population density of the concomitant species. H. columbus suppressed M. incognita populations in the soil nonlinearly, but M. incognita had no effect on H. columbus.     

The Relationship Between Soil Populations of Meloidogyne incognita and Yield Reduction of Soybean in the Coastal Plain

In a replicated field plot experiment, the population density of Meloidogyne incognita was monitored biweekly through the overwintering period (December through April) between soybean crops. The population survived as second-stage juveniles whose numbers remained stable through the winter months and did not decline until February. The yields of plots planted with a M. incognita susceptible cultivar were negatively correlated with the numbers of juveniles recovered at all preplanting sampling dates. In the mid-winter period (December through February), a regression equation describing the relationship predicted a yield reduction (slope) equivalent to 5.36 kg/ha for each juvenile in a 10-cm³ soil sample. In two subsequent field experiments, conducted in different sites and years, mid-winter (November) sampling gave yield reduction predictions of 4.65 and 6.69 kg/ha. Tests of the null hypothesis gave no evidence to indicate that the three slopes differed (P = 0.05). A regression analysis of combined data from the three experiments determined a mid-winter predictive yield reduction of 5.31 kg/ha for each juvenile in the 10-cm³ sample. As the sampling time approached the planting date, there were changes in the predictive yield reductions due to each juvenile in a sample. These are best described by the equation, $\widehat{\gamma }$ (yield loss) = 54.47 - 0.67X + 0.0023X², where X equals the days remaining between sampling and planting. Soil sampling should be performed during mid-winter (November through January) for the most reliable prediction of soybean yield loss.     

Relationship between Meloidogyne incognita and Rotylenchulus reniformis as Influenced by Soybean Genotype

The effect of soybean genotype on competition between Meloidogyne incognita race 2 (Mi) and Rotylenchulus reniformis (Rr) was evaluated in greenhouse and microplot replacement series experiments. Soil in pots containing seedlings of ''Davis'' (susceptible to Mi) or ''Buckshot 66'' (resistant to Mi) was infested with 1,000 vermiform individuals in the following Mi:Rr ratios: 0:0, 100:0, 75:25, 50:50, 25:75, or 0:100. After 91 days, the relative nematode yields (number of nematodes in mixed culture divided by the number in nonmixed culture) of each species were calculated based on soil and root nematode populations expressed as nematodes per gram of dry root tissue. To define the relationship between the two species, calculated relative nematode yields were compared with a theoretical noncompetition model using lack-of-fit regression. In the greenhouse, Mi populations on ''Davis'' were stimulated in the presence of Rr. In microplots, low Mi and Rr population densities likely resulted from severe galling and destruction of feeder roots that probably occurred early in the season. Enhanced susceptibility to Mi was not observed on ''Buckshot 66'', which remained resistant to Mi even when colonized by Rr. Host resistance is a key factor in determining the nature of the relationship between Mi and Rr.     

Cellular Responses of Resistant and Susceptible Soybean Genotypes Infected with Meloidogyne arenaria Races 1 and 2

The cellular responses induced by Meloidogyne arenaria races 1 and 2 in three soybean genotypes, susceptible CNS, resistant Jackson, and resistant PI 200538, were examined by light microscopy 20 days after inoculation. Differences in giant-cell development were greater between races than among the soybean genotypes. M. arenaria race 1 stimulated small, poorly formed giant-cells in contrast with M. arenaria race 2, which induced well-developed, thick-walled, multinucleate giant-cells. The number of nuclei per giant-celt was variable, but fewer nuclei were usually present in giant-cells induced by race 1 (mean 16 nuclei) than in giant-cells induced by race 2 (mean 41 nuclei). Differences observed in giant-cell development were related to differences in growth and maturation of M. arenaria races 1 and 2 and host suitability of the soybean genotypes.     

Population Development of Meloidogyne incognita on Soybean Defoliated by Pseudoplusia includens

Greenhouse studies examined population densities of Meloidogyne incognita race 4 on soybean (Glycine max ''Davis'') defoliated by larvae of soybean looper (Pseudoplusia indudens (Walker)). Plants were defoliated over a 2-week period beginning 5 weeks after seedlings were transplanted. Four groups of plants were infested with nematodes (5,000 eggs/pot) at 2-week intervals to allow harvesting of plants at 0, 2, 4, and 6 weeks postdefoliation (WPD). Plants in each group were harvested 4 weeks after nematode infestation. Root and nodule weights of defoliated plants were suppressed at 0 WPD, but differences were not detectable at 2, 4, and 6 WPD. Population densities of M. incognita were similar on defoliated and control plants at 0 WPD but were greater on defoliated plants at 4 and 6 WPD. Percentage hatching of eggs produced on the latter plants also was higher. Effects of insect-induced defoliation on development of M. incognita remained detectable even after soybean plant growth apparently returned to normal.     

Effects of Temperature,Plant Age,Soil Texture,and Meloidogyne incognita on Early Growth of Soybean

A digitizer-microcomputer combination was utilized to determine soybean seedling response to population densities of M. incognita (Mi) under varied environmental conditions. Plant age, temperature, soil texture, and initial Mi inoculum (Pi) influenced the pattern of shoot and root growth. Effects of Mi on plant top growth were evident on plants inoculated 2 days after seeding, but generally were not noticeable on those receiving Mi after 4, 6, or 8 days (observations limited to 6 days after inoculation). The greatest Pi of Mi (16,700 juveniles/plant) suppressed root growth on plants inoculated at 2 or 4 days after seeding. Mi had no impact on root growth at 22 C on plants inoculated 6 or 8 days after seeding at any temperature used (22, 26, 30 C). New root initiation was inhibited on soybeans inoculated 2 days after seeding at the highest Pi at all three temperatures, but only at 30 C for a Pi of 1,670 juveniles/plant. Growth of first order lateral roots and general root length were suppressed by Mi on the youngest (2-day) plants. However, a low Pi (167 juveniles/ plant) resulted in root proliferation on 4-day-old plants at 26 C. Mi was most damaging in a low clay-content soil mixture.     

Response of Resistant Soybean Plant Introductions to Meloidogyne incognita in Field Microplots

The response of two soybean plant introductions, PI 96354 and PI 417444, highly resistant to Meloidogyne incognita, to increasing initial soil population densities (Pi) (0, 31, 125, and 500 eggs/100 cm³ soil) of M. incognita was studied in field microplots for 2 years. The plant introductions were compared to the cultivars Forrest, moderately resistant, and Bossier, susceptible to M. incognita. Averaged across years, the yield suppressions of Bossier, Forrest, PI 417444, and PI 96354 were 97, 12, 18, and < 1%, respectively, at the highest Pi when compared with uninfested control plots. Penetration of roots by second-stage juveniles (J2) increased linearly with increasing Pi at 14 days after planting. At the highest Pi, 62% fewer J2 were present in roots of PI 96354 than in roots of the other resistant genotypes. Soil population densities of M. incognita were lower on both plant introductions than on Forrest. At 75 and 140 days after planting, PI 96354 had the lowest number of J2 in the soil, with 49% and 56% fewer than Forrest at the highest Pi. The resistance genes in PI 96354 should be useful in a breeding program to improve the level of resistance to M. incognita in soybean cultivars.     

Influence of Soil Temperature on Meloidogyne incognita Resistant and Susceptible Cotton,Gossypium hirsutum

The degree of resistance by a cotton plant to Meloidogyne incognita is affected by soil temperature, particularly in moderately resistant cultivars, The total number of nematodes in the resistant and moderately resistant rools at 35 C was equal to, or greater than, the number in susceptible roots at 20, 25, or 30 C. A shift in numbers to developing and egg-bearing forms of nematodes in the susceptible cultivar as tentperature increased indicates development was affected by temperature rather than by genetic resistance mechanisms. However, the nematode resistant cultivar did not support maturation of nematodes until a soil tempurature of 35 C was attained. This indicated that resistance mechanisms are partially repressed at 35 C and differences in nematode development cannot be explained in terms of accumulated heat units. The moderately resistant cultivar was significantly more sensitive to the effects of high temperature than was the resistant cultivar.     

Influence of Meloidogyne incognita on Resistant and Susceptible Sweet Potato Cultivars

Effects of several population densities ofMeloidogyne incognita on the sweet potato cultivars Centennial (susceptible) and Jasper (moderately resistant) were studied. Field plots were infested with initial levels (Pi) of 0, 10, 100, 1,000, 5,000, and 10,000 eggs and juveniles/500 cm³ soil in 1980 and 0, 100, 1,000, 2,000, 3,000, 4,000, and 5,000 in 1981. M. incognita population development trends were similar on both cultivars; however, at high Pi, more eggs and juveniles were recovered from Centennial than from Jasper. The highest Pi did not result in the highest mid-season (Pm) counts. Pi was negatively correlated with the number of marketable roots and root weight but positively correlated with total cracked roots, percentage of cracked roots, and cracking severity. Jasper tolerated higher Pi with greater yields and better root quality than Centennial. Cracking of fleshy roots occurred with both cultivars at low Pi.     

Aggressiveness and Reproduction of Four Meloidogyne arenaria Populations on Soybean

Aggressiveness and reproduction differed among four geographical populations of M. arenaria on six soybean cultivars in field microplots. These differences were consistent over 3 years. The populations did not differ in virulence; i.e., population by cultivar interactions were not significant. Perineal pattern morphology, the North Carolina differential host test, chromosome counts of immature oocytes, and esterase phenotypes confirmed that the four populations were M. arenaria. Three populations were host race 2 and one population was host race 1.     

Effects of Heterodera glycines and Meloidogyne incognita on Early Growth of Soybean

Greenhouse and field microplot studies were conducted to compare soybean shoot and root growth responses to root penetration by Heterodera glycines (Hg) and Meloidogyne incognita (Mi) individually and in combination. Soybean cultivars Centennial (resistant to Hg and Mi), Braxton (resistant to Mi, susceptible to Hg), and Coker 237 (susceptible to Hg and Mi) were selected for study. In the greenhouse, pot size and number of plants per pot had no effect on Hg or Mi penetration of Coker 237 roots; root weight was higher in the presence of either nematode species compared with the noninoculated controls. In greenhouse studies using a sand or soil medium, and in field microplot studies, each cultivar was grown with increasing initial population densities (Pi) of Hg or Mi. Interactions between Hg and Mi did not affect early plant growth or number of nematodes penetrating roots. Root penetration was the only response related to Pi. Mi penetration was higher in sand than in soil, and higher in the greenhouse than in the field, whereas Hg penetration was similar under all conditions. At 14 days after planting, more second-stage juveniles were present in roots of susceptible than in roots of resistant plants. Roots continued to lengthen in the greenhouse in the presence of either Mi or Hg regardless of host genotype, but only in the presence of Mi in microplots; otherwise, responses in field and greenhouse studies were similar and differed only in magnitude and variability.     

The Influence of Temperature on Meloidogyne incognita on Soybean

The effects of temperature and initial inoculum density of Meloidogyne incognita on soybean growth and nematode reproduction were investigated in greenhouse temperature tanks and in controlled-growth chambers. The interactions of initial inoculum density (P_i) and soil temperature in effects on shoot growth were adequately described by multiple-regression models. At the highest temperatures (30 or 32/28 C), moderate to high inoculum killed many plants. A P_i of 27,000 eggs/15-cm-diam pot retarded shoot growth at 26 C. Only the greatest P_i (81,000 eggs/15-cm pot) suppressed shoot growth at 18, 22, or 20/16 C. Inoculation with 3,000 or 9,000 eggs/plant resulted in heavier root systems at all temperatures except 30 C. At that temperature, 9,000 eggs suppressed root growth. At 18 and 26 C, a Pi of 81,000 eggs was required to retard root growth. Nematode reproduction was related directly to temperature and P_i except at a density of 81,000 eggs/15-cm pot.