Effect of Soil Temperature on Reproduction of Root-knot Nematodes in Flue-cured Tobacco with Homozygous Rk1 and/or Rk2 Resistance Genes.

Most commercial flue-cured tobacco cultivars contain the Rk1 resistance gene, which provides resistance to races 1 and 3 of Meloidogyne incognita and race 1 of M. arenaria. A number of cultivars now possess a second root-knot resistance gene, Rk2. High soil temperatures have been associated with a breakdown of root-knot resistance genes in a number of crops. Three greenhouse trials were performed from 2014 to 2015 investigate the effect of high soil temperature on the efficacy of Rk1 and/or Rk2 genes in reducing parasitism by a population of M. incognita race 3. Trials were arranged in randomized complete block design in open-top growth chambers set at 25°, 30°, and 35°C. Plants were inoculated with 3,000 eggs and data were collected 35 days post-inoculation. Galling, numbers of egg masses and eggs, and reproductive index were compared across cultivar entries. Nematode reproduction was reduced at 25°C and 30°C on entries possessing Rk1 and Rk1Rk2 compared to the susceptible entry and the entry possessing only Rk2. However, there were often no significant differences in reproduction at 35°C between entries with Rk1 and/or Rk2 compared to the susceptible control, indicating an increase of root-knot nematode parasitism on resistant entries at higher temperatures. Although seasonal differences in nematode reproduction were observed among experiments, relative differences among tobacco genotypes remained generally consistent.

Additional notes on the morphology and molecular data of the Kikuyu root-knot nematode, Meloidogyne kikuyensis (Nematoda: Meloidogynidae).

Females, males, and second-stage juveniles of Meloidogyne kikuyensis were examined by light and scanning electron microscopy. The morphology of M. kikuyensis was typical for species of the genus in general, but differed in several characters, appearing to be in a more primitive state. The head morphology of males and second-stage juveniles of most species of root-knot nematode is made up of a large labial disk surrounded by the fused pairs of the sub-dorsal and sub-ventral lips, but in M. kikuyensis, the labial disk is surrounded by six distinct lips. Second-stage juveniles appear to develop similarly to that of other members of the genus. The division of the egg seems to be quite different from typical species in that two small, highly refractive cells, are set-aside early in embryogenesis. Elucidation of the mitochondrial nucleotide sequence for the cytochrome oxidase subunit II and the large subunit of the ribosomal RNA gene (COII-16S rRNA) and the ITS1 region implicated M. kikuyensis is in a basal position when compared to other species of the genus.

Meloidogyne aegracyperi n. sp. (Nematoda: Meloidogynidae), a root-knot nematode parasitizing yellow and purple nutsedge in New Mexico.

Meloidogyne aegracyperi n. sp. is described from roots of purple nutsedge in southern New Mexico, USA. Mature females are small (310-460 µm), pearly white, with their egg masses completely contained inside root galls. The neck is often at a 90 to 130° angle to the protruding posterior end with the perineal pattern. The distance of the dorsal esophageal gland orifice (DGO) to the base of the stylet is relatively long (4.0-6.1 µm), and the excretory pore is level with the base of the stylet. The anterior portion of the rounded lumen lining of the metacorpus contains 3 to 10 small vesicles. The perineal pattern has a rounded dorsal arch with a tail terminal area that is smooth or marked with rope-like striae. Only two males were found. The body twists 90° throughout its length. The DGO to the base of the stylet is long (3.0-3.3) µm. The cephalic framework of the second-stage juvenile is weak, and the stylet is short (10.1-11.8 µm). The DGO to the base of the stylet is long (3-5 µm). The tail is very long (64-89 µm) and the hyaline portion of the tail is very narrow, making the tail finely pointed. Eggs are typical for the genus and vary in length (85.2-99.8 µm) and width (37.1-48.1 µm), having a L/W ratio of (2.1-2.6). Maximum likelihood phylogenetic analyses of the different molecular loci (partial 18S rRNA, D2-D3 of 28S rRNA, internal transcribed spacer (ITS) rRNA, cytochrome oxidase subunit II (COII)-16S rRNA of mitochondrial DNA gene fragments and partial Hsp90 gene) placed this nematode on an independent branch in between M. graminicola and M. naasi and a cluster of species containing M. chitwoodi. M. fallax, and M. minor. Greenhouse tests showed that yellow and purple nutsedge were the best hosts, but perennial ryegrass, wheat, bentgrass, and barley were also hosts.

Reproduction of Meloidogyne incognita Race 3 on Flue-cured Tobacco Homozygous for Rk1 and/or Rk2 Resistance Genes.

Most commercial tobacco cultivars possess the Rk1 resistance gene to races 1 and 3 of Meloidogyne incognita and race 1 of Meloidogyne arenaria, which has caused a shift in population prevalence in Virginia tobacco fields toward other species and races. A number of cultivars now also possess the Rk2 gene for root-knot resistance. Experiments were conducted in 2013 to 2014 to examine whether possessing both Rk1 and Rk2 increases resistance to a variant of M. incognita race 3 compared to either gene alone. Greenhouse trials were arranged in a completely randomized design with Coker 371-Gold (C371G; susceptible), NC 95 and SC 72 (Rk1Rk1), T-15-1-1 (Rk2Rk2), and STNCB-2-28 and NOD 8 (Rk1Rk1 and Rk2Rk2). Each plant was inoculated with 5,000 root-knot nematode eggs; data were collected 60 d postinoculation. Percent galling and numbers of egg masses and eggs were counted, the latter being used to calculate the reproductive index on each host. Despite variability, entries with both Rk1 and Rk2 conferred greater resistance to a variant of M. incognita race 3 than plants with Rk1 or Rk2 alone. Entries with Rk1 alone were successful in reducing root galling and nematode reproduction compared to the susceptible control. Entry T-15-1-1 did not reduce galling compared to the susceptible control but often suppressed reproduction.

Heat Tolerance and Aging of the Anhydrobiotic Seed Gall Nematode with SEM Observations.

The seed gall nematode, Anguina agrostis, feeds and reproduces within the developing ovaries of bentgrass seeds and overwinters in seed galls as anhydrobiotic juveniles. These dormant juveniles can survive within the seed gall for many years. In this dehydrated state, they are more tolerant to extreme environmental conditions than are their hydrated counterparts. Nematodes in seed galls were exposed to various high temperatures (80 to 160°C) for time intervals of 5 to 30 min. Survival decreased as time and temperature increased. Remarkably, these nematodes survived exposure to 155°C for 5 min, higher than that recorded for any other metazoan. In contrast, seed galls that had been stored at room temperature and humidity for 5 yr also survived exposure to extreme temperatures; however, their survival rates were not as high as those for freshly collected galls. Juveniles within the seed gall were coiled and grouped together conforming to the shape of the seed gall. The gross morphology of the cuticle of the juveniles was very smooth and relatively undistorted by the shrinkage from the loss water from their body tissues. Wherever the nematodes were cut with a razor blade, a small amount of their contents oozed out of the opening and coalesced with that of other nearby specimens and appeared gel-like. Elucidation of the mechanisms that enable these nematodes to remain viable after exposure to extreme heat remains a mystery. Understanding the changes that occur in these nematodes as they rehydrate and return to life from an ametabolic state may have major impacts on the life sciences, including insights into the answer of the age-old question: "What is life?"

Induction and Maintenance of Systemic Acquired Resistance by Acibenzolar-S-Methyl in Three Cultivated Tobacco Types.

Induction and maintenance of systemic acquired resistance (SAR) in 'N' gene containing burley, flue-cured, and oriental tobacco cultivars were assessed by monitoring decreases in the number of local lesions caused by Tobacco mosaic virus (TMV) following treatment with acibenzolar-S-methyl (ASM). Leaf samples were collected from lower, middle, and top positions on seedlings at 3-day intervals over 21 days following ASM treatment and subsequent inoculation with TMV under laboratory conditions. Local lesion number for each leaf was recorded 7 days postinoculation. Reductions in TMV local lesion numbers on ASM-treated versus nontreated tobacco varied over time, and differed for each tobacco type. Based on reduced local lesion numbers, SAR was induced in burley and flue-cured tobacco by 3 and 6 days postinoculation, respectively, while oriental tobacco responded by 9 days. SAR was maintained in burley tobacco from 3 to 9 days after ASM application, and from 9 to 15 days after application in oriental tobacco. ASM treatment reduced local lesion numbers in flue-cured tobacco significantly at 6, 12, and 21 days postapplication, but not at 15 and 18 days after treatment. The SAR response was similar among lower, middle, and top leaves with no effect of ASM on response by leaf position, although TMV local lesion numbers were greater on lower leaves than on middle and top leaves 6 days after treatment, but significantly less on lower leaves 18 days after treatment compared to middle and top leaves.

A technique for making high-resolution megapixel mosaic photomicrographs of nematodes.

Multiple images of a whole nematode specimen were taken with a high power oil-immersion objective lens and joined together to form one high-resolution megapixel, mosaic photomicrograph of the entire specimen, with the use of a relatively new mounting technique made with a 4% water agar pad. The agar pad kept the specimen nearly level and lateral, and when amended with 10 mM sodium azide, this mounting technique gradually paralyzed the nematode in a natural pose to enable production of sharp, clear images. The individual photographs were joined together and merged into one very large, seamless image. These montaged images will be useful for teaching because the student has access to a virtual specimen that is mounted in the correct orientation, imaged with a research grade microscope, and preserved in a narcotized, living condition. Such specimen images can also serve as representatives of type and voucher specimens without the deterioration typical of real types. The files can be copied and viewed with a computer almost anywhere and at any time, rather than using a more cumbersome, limiting, and expensive microscope.

Description of a Unique, Complex Feeding Socket Caused by the Putative Primitive Root-Knot Nematode, Meloidogyne kikuyensis.

Meloidogyne kikuyensis produces unique galls that form on one side of the root resembling nitrogen-fixing nodules that are produced on legumes in response to infection by Rhizobium and related bacteria. The gall caused by this root-knot nematode is made up of a complex feeding socket composed of several giant cells that are ramified with xylem vessels extending perpendicular from the vascular cylinder. The anterior portion of the second-stage juvenile, which develops into an adult, plugs into this unique feeding socket. The socket and the surrounding parenchyma together form a gall that is very different in morphology from those typically caused by other species of root-knot nematodes. Even though M. kikuyensis was considered to be a primitive species because of its low chromosome count, the complexity of its feeding site and minor plant damage suggests a more derived systematic position.

Widespread Distribution of Fungivorus Aphelenchoides spp. in Blight Cankers on American Chestnut Trees.

Previously we showed in laboratory studies that the fungivorus nematode, Aphelenchoides hylurgi, was attracted to and fed upon the chestnut blight fungus, Cryphonectria parasitica, from American chestnut bark cankers and was a carrier of biocontrol, white hypovirulent C. parasitica strains. In the present field study, we recovered Aphelenchoides spp. in almost all (97.0 %) of 133 blight canker tissue assays (three 5-g samples each) from four eastern states. High mean population densities (227 to 474 nematodes per 5 g tissue) of Aphelenchoides spp. were recovered from cankers in Virginia, West Virginia, and Tennessee but not from New Hampshire (mean = 75 nematodes per 5 g tissue). Overall, most canker assays yielded population densities less than 200 nematodes per 5 g tissue. All of 12 very small or young cankers yielded a few to many Aphelenchoides spp. Regression analysis indicated greatest recovery of Aphelenchoides spp. occurred in the month of May (r = 0.94). The results indicate that Aphelenchoides spp. appear to be widespread in blight cankers on American chestnut trees and could play a role in biocontrol of chestnut blight.

Epidemics of Meloidogyne brasilensis in Central Brazil on Processing Tomato Hybrids That Have the Root-Knot Nematode Mi Resistance Gene.

The species Meloidogyne brasilensis Charchar & Eisenback 2002 was described as causing root rot, severe wilt, and numerous galls in pea (Pisum sativum L.) in Brasília-Federal District and tomato (Solanum lycopersicum L.) cv. Rossol (known to have the root-knot nematode resistance Mi gene) in Londrina-Paraná State, Brazil. To our knowledge, this current work is the first report of the epidemics on tomato hybrids that have the Mi gene caused by infection of M. brasilensis in central Brazil. Samples were obtained from fields with two commercial hybrids that have the Mi gene ('Calroma' and 'Nemapride') that were cultivated under center-pivot irrigation in Silvânia, Goiás State. These hybrids exhibited slow vegetative development and malformed roots because of the high number of large galls. Symptomatic plants were collected from a tomato crop area of more than 100 ha. Random sampling indicated field sectors with up to 100% of symptomatic plants. Morphological and morphometric evaluations of this Meloidogyne population were carried out with the female perineal pattern, stylet, and excretory pore and also with the male body traits, labial disc, and stylet. The esterase phenotype was unique for this population with four clear bands (J. M. Charchar, unpublished data). Altogether, the morphological and biochemical characteristics of this population were in agreement with that reported for M. brasilensis (1). Koch's postulates were fulfilled using tomato 'Rutgers' (susceptible) and 'Rossol' (with the Mi resistance locus) under greenhouse conditions. The massive use of tomato hybrids with the Mi gene could be a strong selection factor favoring this pathogen under growing conditions in central Brazil. Germplasm screen searching for sources of resistance specific to this nematode species is advisable. Reference: (1) J. M. Charchar and J. D. Eisenback. Nematology 4:629, 2002.

European corn borer (Lepidoptera: Crambidae) stalk tunneling on root-knot nematode (Tylenchida: Heteroderidae) fitness on corn.

Greenhouse experiments were conducted in 2004-2006 to examine the reciprocal effects of aboveground herbivory by European corn borer, Ostrinia nubilalis (Hübner) (Lepidoptera: Crambidae), and belowground herbivory by root-knot nematode, Meloidogyne incognita Chitwood (Tylenchida: Heteroderidae), on one another at three corn, Zea mays L., growth stages. Two experiments were conducted to study the effect of aboveground herbivory by O. nubilalis on the number of M. incognita juvenile penetration/root system and eggs/root system. In the first experiment, the O. nubilalis infestation level by plant growth stage main effect interaction was not significant for either M. incognita juvenile penetration or eggs. The overall effect of stalk tunneling by O. nubilalis resulted in 48.9% fewer juvenile penetration and 40.0% fewer eggs than in the respective controls. In the second experiment, the main effects interaction was significant for juvenile penetration (P = 0.0422) and eggs (P = 0.0134). At the eight- and 10-leaf growth stages, the combined effect of one and three O. nubilalis larvae per plant resulted in 41.2 and 44.7% significantly fewer juvenile penetration than in the respective controls. Similarly, the combined effect of stalk tunneling (with the exception of one larvae per plant at the 10-leaf growth stage) at the six-, eight-, and 10-leaf growth stages resulted in 46.3, 53.3, and 55.2% fewer eggs than in the respective controls. In all instances, M. incognita juvenile penetration and eggs were significantly negatively correlated with O. nubilalis tunnel length. In a reciprocal experiment conducted two times, no significant (P > 0.05) effect of M. incognita inoculation level on stalk tunneling was found in either experiment.

Aphelenchoides hylurgi as a carrier of white, hypovirulent Cryphonectria parasitica and its possible role in Hypovirulence spread on blight-controlled american chestnut trees.

Individual nematodes were isolated from American chestnut blight-controlled cankers to determine if they were carriers of biocontrol (hypovirulent) isolates of the chestnut blight fungus, Cryphonectria parasitica. These hypovirulent isolates have a white fungal colony phenotype due to infection by the virus CHV1. Of 1,620 individual Aphelenchoides hylurgi isolated, 29.4% carried propagules of the blight fungus and 8.2% of these yielded white hypovirulent isolates. In attraction and movement tests in Petri plates, A. hylurgi moved 2 cm over 24 hr to mycelial discs of white hypovirulent C. parasitica and pigmented C. parasitica strains in nearly equal numbers. After 2 days of nematode movement to fungal colonies on agar in Petri plates and 21 days of nematode growth, large numbers of A. hylurgi were extracted from both white hypovirulent and pigmented C. parasitica strain colonies. Lower numbers of A. hylurgi were extracted from excised young American chestnut blight cankers that were inoculated with A. hylurgi and incubated for 22 days. A. hylurgi inoculated on the surface of an excised American chestnut canker moved within 24 hr to the small, spore-bearing C. parasitica reproductive structures (stromata) on the canker surface. The results indicate that A. hylurgi may play a role in the spread of hypovirulence on American chestnut trees.

First Report of the Nematode, Tylenchulus palustris, Parasitizing Peach in Virginia.

In the fall of 2005 during routine sampling for plant-parasitic nematodes in a nematicide evaluation trial, juveniles of Tylenchulus palustris Inserra, Vovlas, O'Bannon & Esser, 1988 (1) were recovered by semi-automatic elutriation and centrifugation. Mature, sedentary females were hand picked from infected root tissues. The nematodes were parasitizing peach (Prunus persica (L.) Batsch.) at Crown Orchards Purvis Farm (37°51.638'N 78°43.062'W, elevation 230 m.) on U.S. Highway 29S near Faber, VA. Twelve of eighty samples contained the nematode with a density that varied from 10 to 70 nematodes per 500 ml3 of soil. Such low numbers may have been due to the severe state of decline of the 30+-year-old peach orchard; the stunted and nearly dead trees were being removed at the time of sampling. Ironically, this nematode was discovered by the first author more than 20 years ago in this same location before it was described as a new species; however, additional research is necessary to determine the role that this nematode played in the decline of this orchard. Identification was based on morphology of the female including the postvulval body terminus and morphometrics of 15 second-stage juveniles. Voucher specimens were placed in the Virginia Tech Nematode Collection and voucher cultures are maintained in the Virginia Tech Nematode Culture Collection. T. palustris was originally found in Florida parasitizing Carolina ash (Fraxinus caroliniana Mill.) and saltbush (Baccharis halimifolia L.) (1). This nematode has been reported previously on peach in Alabama, Arkansas, and Georgia (2). References: (1) R. N. Inserra et al. J. Nematol. 20:266, 1988. (2) R. N. Inserra et al. J. Nematol. 22:45, 1990.

First Report of the Barley Root-Knot Nematode Meloidogyne naasi Infecting Annual Bluegrass on a Golf Course in Quebec, Canada.

Annual bluegrass, Poa annua L., is an important component of the vegetation on golf course greens and fairways throughout Canada and is widely distributed across the world (2). The barley root-knot nematode, Meloidogyne naasi Franklin, infects and damages cereals such as barley (Hordeum vulgare), sorghum (Sorghum vulgare), and wheat (Triticum durum and T. vulgare), mainly in Europe. Of the root-knot species, M. naasi in particular, prefers grasses over other hosts, and infestations of this nematode can reduce the growth and vigor of turfgrasses (1). In July 2005, annual bluegrass at Beaconsfield Golf Club in Pointe Claire (45°26'N, 73°50'W), Quebec showed signs of an unidentified disease. Irregular yellowish/chlorotic patches were observed on the collar of one golf green. Lower turfgrass density in the turf areas with symptoms was noted. When roots were examined under a dissecting microscope, galling was observed. Upon dissection of washed galls, root-knot nematode egg masses and mature females inside the roots were observed. Nematode extractions of the soil from two samples of 50 g from the green and around the collar and perimeter were also done by the modified Baermann pan method. No juveniles were recovered from soil samples from the healthy area and an average of 400 and 1,500 juveniles/kg dry soil were counted in collar and perimeter samples of the patches. Morphological identification of mature females and juveniles were performed and confirmed to be M. naasi. Currently, there are no regulations to control the introduction of this nematode into Canada. To our knowledge, this is the first report of the occurrence of M. naasi in Canada where it is causing noticeable damage to turfgrass in Quebec. A soil survey is currently underway to examine the distribution of this nematode on golf course turfgrasses in Ontario and Quebec. References: (1) R. Cook and G. W. Yeates. Nematode pests of grassland and forage crops. Pages 305-350 in: Plant Parasitic Nematodes in Temperate Agriculture. K. Evans et al., eds. CAB International, Wallingford, UK, 1993. (2) S. I. Warwick. Can. J. Plant Sci. 59:1053, 1979.

First Report of Bentgrass Seed Gall Nematode, Anguina agrostis, in Virginia and Minnesota.

On August 24, 2003, during a foray for grasses infected with fungi, redtop creeping bentgrass (Agrostis stolonifera L.) was collected on Butt Mountain Lookout near an abandoned fire tower with coordinates 80°37'40.3″ W and 37°22'14.0″N at an altitude of 1,284 m overlooking the New River between the towns of Pembroke and Ripplemead, VA. Seed heads with very elongated glumes, lemmas, and paleas were very common, and the incidence rate was nearly 95% on the basis of symptomatic plants in the immediate area surrounding the tower comprising more than 5 ha of a grassy meadow. Close examination revealed the occurrence of elongated, blackish galls replacing the ovaries and containing Anguina agrostis (Steinbuch, 1799) Filipjev, 1936. Nematode cultures were established and maintained on red top creeping bentgrass (A. stolonifera) in a greenhouse. Identification was based on morphology and measurements of juveniles L = 407 + 22 (376-418) µ, stylet L = 18.5 + 1.7 (17.0-21.3) µ males L = 351 + 17 (339-367) µm; and females L = 455 + 33. Examination of specimens collected previously by C. Roane revealed that another population of Anguina agrostis was also found on August 9, 1990 parasitizing the same host growing along Echo Trail near Big Lake Lodge Rd. in St. Louis County, MN. The infestation at the Virginia site may have been from sowing infested seeds at the disturbed construction site for the fire lookout tower and other buildings. However, the occurrence at the Minnesota site is less likely to be anthropogenic. Voucher specimens from both locations were placed in the Virginia Tech Nematode Collection, and voucher cultures are maintained in the Virginia Tech Nematode Culture Collection.

Intraspecific Variability within Globodera tabacum solanacearum Using Random Amplified Polymorphic DNA.

Random amplified polymorphic DNA (RAPDs) were used to investigate the intraspecific variability among 19 geographic isolates of Globodera tabacum solanacearum from eight counties in Virginia and one county in North Carolina. Globodera tabacum tabacum, G. t. virginiae, and the Mexican cyst nematode (MCN) were included as outgroups. Six primers were used and 119 amplification products were observed. Each primer yielded reproducible differences in fragment patterns that differentiated the isolates and species. Hierarchical cluster analysis was performed to illustrate the relatedness among isolates and species. The average Jaccard's similarity index among isolates of G. t. solanacearum was 74%, possibly representing greater variation than that reported in the literature across different pathotypes of the potato cyst nematode, Globodera pallida, in studies where RAPD were also employed. The RAPD markers described here may be useful for the development of specific primers or probes that could improve the identification of TCN populations. Such improvements in the characterization of TCN genotypes would facilitate the effective deployment of existing and future resistant cultivars to control these economically important pests.

First Report of the Reniform Nematode Rotylenchulus reniformis on Cotton in Virginia.

In Virginia during September 2002, the reniform nematode, Rotylenchulus reniformis Linford and Oliveira (1), was found for the first time following a grower's concern about poor growth and yield of cotton (Gossypium hirsutum L.) cv. Fiber Max 989BR. The infested field was planted with cotton each year for the last eight growing seasons. The field was located on Hall Road in Southampton County, Virginia at coordinates 77°16'28.8926″W, 36°37'10.6428″N near the town of Branchville. The soil was loamy sand, which is typical of sandy textured soils in the region. Rainfall from May to September at a nearby weather station was nearly 50% below normal, which may have contributed to the suppression of plant growth. The vermiform nematodes were extracted with a North Carolina State University model semiautomatic elutriator and centrifugation/sugar flotation. Populations were 30 to 150 per 500 cm3 of soil in areas with noticeable stunting. Cultures were established on cotton cv. Delta Pine 64 and tomato (Lycopersicon esculentum Mill. cv. Rutgers) and were maintained in a greenhouse. Reproduction was moderate on cotton and high on tomato. Identifications were based on morphology and measurements of vermiform females and males: immature female length (L) = 407 ± 22 (376 to 418) µm, stylet L = 18.5+1.7 (17.0 to 21.3) µm; and male L = 351 ± 17 (339 to 367) µm. Voucher specimens were placed and are maintained in the Virginia Tech Nematode Collection. Reference: (1) M. B. Linford and J. M. Oliveira. Proc. Helminthol. Soc. Wash. 7:35, 1940.

Meloidogyne haplanaria n. sp. (Nematoda: Meloidogynidae), a Root-knot Nematode Parasitizing Peanut in Texas.

Meloidogyne haplanaria n. sp. is described and illustrated from specimens parasitizing peanut in Texas. The perineal pattern of the female is rounded to oval with a dorsal arch that is high and rounded except for striae near the vulva, which are low with rounded shoulders. The striae are distinctly forked in the lateral field, and punctations often occur as a small group near the tail tip and singly within the whole perineal pattern. The female stylet is 13-16 microm long and has broad, distinctly set-off knobs. The excretory pore opens 40-118 microm from the head, approximately halfway between the anterior end and the metacorpus. Males are 1.2-2.4 microm in length and have a high, wide head cap that slopes posteriorly. The labial disc and medial lips are partially fused to form an elongated lip structure. In some specimens the labial disk is distinctly separated from the lips by a groove. The stylet is 17-22 microm long and has wide knobs that are rounded and distinctly set off from the shaft. Mean second-stage juvenile length is 419 microm. The head region is not annulated, and the large labial disc and crescent-shaped medial lips are fused to form a dumbbell-shaped head cap. The stylet is 9-12 microm long and has rounded, posteriorly sloping knobs. The slender tail, 58-74 microm long, has a distinct, inflated rectum and a slightly rounded tip. The hyaline tail terminus is 11-16 microm long. The isozyme phenotypes for esterase and malic dehydrogenase do not correspond to any other recognized Meloidogyne species. Tomato and peanut are good hosts; corn and wheat are very poor hosts; and cotton, tobacco, pepper, and watermelon are nonhosts.

Effects of Host Resistance and Temperature on Development of Globodera tabacum solanacearum.

Penetration and development of juveniles of tobacco cyst nematode (Globodera tabacum solanacearum) on a resistant (NC567) and a susceptible (K326) cultivar of flue-cured tobacco (Nicotiana tabacum L.) were determined in root zone chamber experiments. More vermiform juveniles developed into a swollen shape at 22, 27, and 31 degrees C than at 17 degrees C. Development of flask-shaped nematodes appeared to be similar across tested temperatures (17, 22, 27, and 31 degrees C). General patterns of penetration and development of juveniles in both resistant and susceptible cultivars were similar under all temperatures tested. More vermiform, swollen, and flask-shaped nematodes were found in roots of K326 than in those of NC567. Development from swollen to flaskshaped nematodes appeared to be similar between the two cultivars, although more vermiform juveniles developed into swollen nematodes on K326 than on NC567. Differences in resistance between the two cultivars remained stable across tested temperatures.