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Morpho-biological notes and histopathology, based on LM and SEM observations, of the fig cyst nematode Heteroderafici isolated from Ficuscarica roots, collected in home and public gardens of Apulia region, southern Italy, are described and illustrated. Seventy-five localities throughout the Apulia region were sampled and one-quarter of the sampled localities had fig roots infested with H.fici, with population densities ranging from 44 to 180 cysts/100 ml of soil. All attempts to detect H.fici on ornamental Ficus spp. as well as on imported bonsai in Italy were unsuccessful. Morphometric characters of the Italian population conform to those of the type and re-description populations reported for H.fici. Molecular analysis using ITS, D2–D3 expansion domains of the 28S rRNA, and the partial 18S rRNA sequences of H.fici newly obtained in this study matched well with the corresponding sequences of H.fici present in the GenBank database. Phylogenetic trees confirmed and supported the grouping of H.fici in the Humuli group. Heteroderafici completes its embryogenic development in 14–16 days at 25 °C. Post-invasion development and maturity in the roots of F.carica seedlings is completed in 64–68 days at 25–28 °C with juveniles and adults showing different parasitic habits, being endoparasitic and semi-endoparasitic respectively. The establishment of permanent feeding sites that consist of the formation of large syncytia causes anatomical modification of vascular elements and general disorder in the root stelar structures. Syncytia structures associated with mature females showed different degrees of vacuolisation, numbers of syncytial cells, and contained nuclei and nucleoli which were constantly hypertrophied.

Morpho-biological notes and histopathology, based on LM and SEM observations, of the fig cyst nematode Heterodera fici isolated from Ficus carica roots, collected in home and public gardens of Apulia region, southern Italy, are described and illustrated. Seventy-five localities throughout the Apulia region were sampled and one-quarter of the sampled localities had fig roots infested with H. fici, with population densities ranging from 44 to 180 cysts/100 ml of soil. All attempts to detect H. fici on ornamental Ficus spp. as well as on imported bonsai in Italy were unsuccessful. Morphometric characters of the Italian population conform to those of the type and re-description populations reported for H. fici. Molecular analysis using ITS, D2-D3 expansion domains of the 28S rRNA, and the partial 18S rRNA sequences of H. fici newly obtained in this study matched well with the corresponding sequences of H. fici present in the GenBank database. Phylogenetic trees confirmed and supported the grouping of H. fici in the Humuli group. Heterodera fici completes its embryogenic development in 14-16 days at 25 [degree]C. Post-invasion development and maturity in the roots of F carica seedlings is completed in 64-68 days at 25-28 [degree]C with juveniles and adults showing different parasitic habits, being endoparasitic and semi-endoparasitic respectively. The establishment of permanent feeding sites that consist of the formation of large syncytia causes anatomical modification of vascular elements and general disorder in the root stelar structures. Syncytia structures associated with mature females showed different degrees of vacuolisation, numbers of syncytial cells, and contained nuclei and nucleoli which were constantly hypertrophied.

Morpho-biological notes and histopathology, based on LM and SEM observations, of the fig cyst nematode Heteroderafici isolated from Ficuscarica roots, collected in home and public gardens of Apulia region, southern Italy, are described and illustrated. Seventy-five localities throughout the Apulia region were sampled and one-quarter of the sampled localities had fig roots infested with H.fici, with population densities ranging from 44 to 180 cysts/100 ml of soil. All attempts to detect H.fici on ornamental Ficus spp. as well as on imported bonsai in Italy were unsuccessful. Morphometric characters of the Italian population conform to those of the type and re-description populations reported for H.fici. Molecular analysis using ITS, D2–D3 expansion domains of the 28S rRNA, and the partial 18S rRNA sequences of H.fici newly obtained in this study matched well with the corresponding sequences of H.fici present in the GenBank database. Phylogenetic trees confirmed and supported the grouping of H.fici in the Humuli group. Heteroderafici completes its embryogenic development in 14–16 days at 25 °C. Post-invasion development and maturity in the roots of F.carica seedlings is completed in 64–68 days at 25–28 °C with juveniles and adults showing different parasitic habits, being endoparasitic and semi-endoparasitic respectively. The establishment of permanent feeding sites that consist of the formation of large syncytia causes anatomical modification of vascular elements and general disorder in the root stelar structures. Syncytia structures associated with mature females showed different degrees of vacuolisation, numbers of syncytial cells, and contained nuclei and nucleoli which were constantly hypertrophied.

Severe infections of parsley plants and soil infestations with Meloidogyne javanica during an autumn surveys for the pathogenic root-knot nematode infestations were found in Monopoli at Bari province in Southern Italy. This unusual severe infection of parsley, considered a winter crop, was possibly instigated by a very warm autumn from the previous year. Nematodes were extracted from soil samples according to the Coolen’s method. Morphological analysis (based on stylet length, tail length and shape, adult females perineal pattern, excretory pore position and Ep/stylet ratio) and molecular studies were used for the nematode characterization and identification. In the soil of infested area a severely deformed root systems were observed, showing a galling rate = 2.5 - 4 (scale 0-5) and a soil nematode population densities ranging from 350 to 2,730 eggs and J2 per 5 g of fresh root. M. javanica attack on parsley roots is a limiting factor for plant growth. Considering that curly-leaf parsley varieties resistant to the nematodes are not yet available control strategies must be focused on reduction of soil infestation level below tolerance limit of the target nematode species. Due to the higher cost and reduced availability of fumigant and non-fumigant nematicides, soil solarization, organic amendments or biological control approaches should be preferably used as alternatives., The present work was supported with funds provided by the Italian Ministry of Economy and Finance to the National Research Council for the project “Innovazione e Sviluppo del Mezzogiorno-Conoscenze Integrate per Sostenibilità ed Innovazione del Made in Italy Agroalimentare”, Legge n. 191/2009, and partially by grant AGR- 136 from ‘Consejería de Economía, Innvovación y Ciencia’ from Junta de Andalucía and the European Social Fund.

High infection rates of European holly (Ilex aquifolium) feeder roots by an unknown root-knot nematode were found in a holly forest at Arévalo de la Sierra (Soria province) in northern Spain. Holly trees infected by the root-knot nematode showed some decline and low growth. Infected feeder roots were distorted and showed numerous root galls of large (8–10 mm) to moderate (2–3 mm) size. Morphometry, esterase and malate dehydrogenase electrophoretic phenotypes and phylogenetic trees of sequences within the ribosomal DNA (rDNA) demonstrated that this nematode species differs clearly from other previously described root-knot nematodes. Studies of host-parasite relationships showed a typical susceptible reaction in naturally infected European holly plants, but did not reproduce on a number of cultivated plants, including tomato, grapevine, princess-tree and olive. The species is described here, illustrated and named as Meloidogyne silvestris n. sp. The new root-knot nematode can be morphologically distinguished from other Meloidogyne spp. by: (i) roundish perineal pattern, dorsal arch low, with fine, sinuous cuticle striae, lateral fields faintly visible; (ii) female excretory pore level with stylet knobs, or just anterior to them, EP/ST ratio about 0·8; (iii) second-stage juveniles with hemizonid located 1 to 2 annuli anterior to excretory pore and short, sub-digitate tail; and (iv) males with lateral fields composed of four incisures, with areolated outer bands. Phylogenetic trees derived from maximum parsimony analysis based on 18S, ITS1-5·8S-ITS2 and D2–D3 of 28S rDNA showed that M. silvestris n. sp. can be differentiated from all described root-knot nematode species, and it is clearly separated from other species with resemblance in morphology, such as M. ardenensis, M. dunensis and M. lusitanica.

6 pages, 2 figures.-- Full-text version available at: http://www.ias.csic.es/pcastillo/nematology-6-749-754.pdf, SEM studies on a Meloidogyne baetica population provided additional details of the external morphology for female, male and second-stage juveniles. The labial disc in female and male specimens is fused with the medial lips forming a single structure. In second-stage juveniles the lateral lips are triangular with rounded margins. The amphidial opening for all life stages appears oval to rectangular in shape and is located between the labial disc and lateral lips. Lateral fields of male and second-stage juveniles have four incisures irregularly areolated along the entire body. The results of a host-range study for additional natural hosts of M. baetica conducted in wild olive communities growing at Vejer de la Frontera (Cádiz province) in southern Spain are also reported. Apart from the type host, M. baetica was found to infect two natural woody host plants, lentisc (Pistacia lentiscus) and Aristolochia baetica. Hostparasite relationships in these new hosts confirmed the typical susceptible reaction observed in wild and cultivated olives. Similarly, the reproductive fitness, evaluated as the number of eggs per egg mass, was not significantly different in all plant hosts. No infections or galled roots were observed in herbaceous plant species studied and M. baetica must therefore be considered as a parasite of woody plants.

Morphological and molecular analyses of a stem nematode causing a severe disease on infected sowthistle (Sonchus bulbosus) plants, involving the formation of gall-like structures on infected leaves and stems, have led to the description of a new species named Ditylenchus oncogenus n. sp. Morphologically, the new species is characterized by a medium to large body size (all adults more than 1 mm in length); a delicate stylet (9.0–11.0 μm long) with minute, rounded knobs; a long post-vulval uterine sac (c. 65% of the vulva–anus distance); six incisures at the lateral fields and characteristic D. destructor-pattern of spicules (with pronounced ventral tumulus and anteriorly pointed, less sclerotized, cuticle parts present within the lamina). The results of molecular analysis of rRNA gene sequences, including the D2–D3 expansion regions of 28S rRNA, internal transcribed spacer (ITS) rRNA, partial 18S rRNA gene, the protein-coding mitochondrial gene, cytochrome oxidase c subunit I (COI), and the heat-shock protein 90 (hsp90) gene, support the new species status. The results of a host-suitability test indicated that the new species does not parasitize potato (Solanum tuberosum) tubers and broad bean (Vicia faba) seedlings. Histopathological observations on naturally infected sowthistle tissues revealed that D. oncogenus n. sp. causes floral stem neoplasia and midrib leaf gall formation on the type, and to date only known, host. The galls were characterized by extensive hyperplasia, where several necrotic cells in the neoplasic area were directly damaged by feeding of the nematode, whereas a number of adjacent cells showed typical cytological changes, such as granulated cytoplasm with hypertrophied nuclei and nucleoli., The present work was supported with funds provided by the Italian Ministry of Economy and Finance to the National Research Council for the project ‘Innovazione e Sviluppo del Mezzogiorno' – Conoscenze Integrate per Sostenibilità ed Innovazione del Made in Italy Agroalimentare – Legge n. 191/2009, and partially by grant AGR-136 from ‘Consejería de Economía, Innvovación y Ciencia’ from Junta de Andalucía and and Union Europea, Fondo Europeo de Desarrollo regional, ‘Una manera de hacer Europa’.

Morphologial, biochemical, molecular and karyological analyses of different populations and races of the stem and bulb nematode Ditylenchus dipsaci have suggested that it represents a species complex, of which only D. dipsaci sensu stricto and its morphologically larger variant, known as the giant race of the stem and bulb nematode, are plant parasites of economic importance. The present study singles out the giant race from this complex, herein described as a new species named Ditylenchus gigas n. sp., on the basis of morphological and molecular data obtained from several populations collected from broad beans in southern Italy, southern Spain and Lebanon. The new species epithet, which refers to the large body size of the nematode with respect to the normal races, must be considered to be conspecific with the D. dipsaci ‘giant race’ from Fabaceae in recent literature. Morphologically, the new species is characterized by a body size 1Æ5–2 times longer than the ‘normal race’, stylet delicate (11Æ5–13Æ0 lm long) with knobs distinctly sloping backwards, and long post-vulval uterine sac (81–150 lm long). Results of molecular analysis of rDNA sequences including the ITS1-5.8S-ITS2 region, the D2–D3 fragment of the 28S gene, the small 18S subunit, the partial mitochondrial gene for cytochrome c oxidase I (mtCOI), and hsp90 gene sequences, support the new taxonomic species status for the former D. dipsaci giant race from Vicia faba, and clearly distinguish D. gigas n. sp. from D. dipsaci sensu stricto.

3 páginas, 2 figuras., A root-knot nematode was frequently detected on the roots of peony (Paeonia lactiflora Pall.) in northern Italy, inducing typical spherical galls with large egg masses (each averaging 320-350 eggs). According to its typical cuticular perineal pattern, esterase and malate dehydrogenase phenotypes, and morphological observations on adults and juveniles, the nematode was identified as Meloidogyne hapla. Galls induced by the nematode on the roots of peony were variable in size but relatively small (only two to three times the healthy root diameter), located mostly along the root axis and less frequently at the root tips. Numerous lateral roots arising from galled main roots were also galled. Comparative histopathological observations of healthy and M. hapla-infected roots of peony showed cellular alterations induced by the nematode in the cortex, pericycle and vascular parenchyma. Permanent feeding sites of the nematode within root tissues consisted of 3-8 giant polynucleate cells surrounding the lip region of females., Work partially supported by the project FLORPRO - CRA FSO (Sanremo, Italy).

The occurrence of a male-less population of Sphaeronema alni parasitising chestnut (Castanea sativa) roots and inducing a stelar syncytium is reported for the first time in Pola de Somiedo (Oviedo province), Spain.Morphometric and molecular characters of the Spanish population matched those of a topotype population from Russia. SEM observations showed swollen females having the first lip annulus wider than the second and appearing as a cap-like, circumoral elevation. The second-stage juveniles, having a single band in the lateral fields, were characterised by a non-annulated dome-shaped lip region derived from the fusion of the oral disc with all the lip sectors and lip annuli, and showing slit-like amphidial apertures and an oval prestoma. The sequences of the D2-D3 expansion segments of 28S rRNA, partial 18S rRNA and ITS rRNA gene for the Spanish and topotype populations of S. alni were congruent and matched those deposited in GenBank for another population from Germany, thereby confirming their conspecificity. A PCR-RFLP profile of D2-D3 of 28S rRNA for identification of this species was also provided. The phylogenetic relationships between S. alni populations and representatives of the suborder Criconematina, as inferred from analysis of partial 18S rRNA and D2-D3 of 28S gene sequences obtained in this and previous studies, indicated that S. alni formed a basal clade on the majority consensus Bayesian phylogenetic trees, standing together with Meloidoderita sp. or alone. These findings provide additional evidence of the need to clarify the position of Sphaeronema within Criconematina and its relationships with representatives of Tylenchulinae.

7 pages., Stunted growth of sweet basil (cv. Genovese) associated with large patches and severe soil infestations by the root-knot nematode Meloidogyne arenaria race 2 were observed in open fields at the end of the crop-growing season in Albenga, province of Savona, Northern Italy by early September 2007. Observed morphological traits of nematode life stages and results of analysis of isozyme electrophoretic patterns and differential host tests were used for nematode species and race identification. Nematode-induced mature galls (either in naturally infected plants or in artificially inoculated root tissues) were spherical or ellipsoidal and confluent along the root axis, containing usually several females, males, and egg-masses with eggs. Feeding sites were characterized by the development of giant cells that contained several hypertrophied nuclei and nucleoli. Giant cell cytoplasm was aggregated along the thickened cell walls. Vascular elements within galls appeared disorganized and disrupted. Due to the heavy damage observed, the relationships between the initial population density and growth of basil plants was also tested in a greenhouse experiment in which inoculum levels varied from 0 to 512 eggs and juveniles/cm3 of soil. Height and top fresh weight data of the inoculated and control plants was fitted to Seinhorst's model. Tolerance limits with respect to plant height and fresh top weight of basil cv. Genovese plants to M. arenaria race 2 were estimated as 0.15 eggs and juveniles/cm3 of soil. The minimum relative values (m) for plant height and top fresh weight were 0.39 and 0.19 at initial nematode population density (Pi) ≥16 eggs and juveniles/cm3 of soil, respectively. The maximum nematode reproduction rate (Pf/Pi) was 448.7 times at an initial population density of 4 eggs and second-stage juveniles/cm3 of soil.

7 pages, 2 figures., Pathogenicity and host-parasite relationships in root-knot disease of celery (Apium graveolens) caused by Meloidogyne incognita race 1 were studied under glasshouse conditions. Naturally and artificially infected celery cv. D'elne plants showed severe yellowing and stunting, with heavily deformed and damaged root systems. Nematode-induced mature galls were spherical and/or ellipsoidal and commonly contained more than one female, males and egg masses with eggs. Feeding sites were characterized by the development of giant cells that contained granular cytoplasm and many hypertrophied nuclei. The cytoplasm of giant cells was aggregated along their thickened cell walls and consequently the vascular tissues within galls appeared disrupted and disorganized. The relationship between initial nematode population density (Pi) and growth of celery plants was tested in glasshouse experiments with inoculum levels that varied from 0 to 512 eggs and second-stage juveniles (J2) mL−1 soil. Seinhorst's model y = m + (1 – m)z^(P–T) was fitted to height and top fresh weight data of the inoculated and control plants. The tolerance limit with respect to plant height and fresh top weight of celery to M. incognita race 1 was estimated as 0·15 eggs and J2 mL−1 soil. The minimum relative values (m) for plant height and top fresh weight were 0·37 and 0·35, respectively, at Pi ≥ 16 eggs and J2 mL−1 soil. The maximum nematode reproduction rate (Pf/Pi) was 407·6 at an initial population density (Pi) of 4 eggs and J2 mL−1 soil.

10 pages, 6 figures.-- PMCID: PMC2586475., Diagnosis of an Argentinean population of Nacobbus sp. infecting sweet pepper (lamuyo) was carried out including morphology, scanning electron microscopy, and molecular studies. In light of our morphometric, molecular and host-range results, we consider the studied population to belong to N. aberrans s. l., and by host range tests the population is assigned to the "sugar beet group." ITS-PCR analysis on individual male and immature female specimens of this population yielded amplification products of approximately 922 bp. RFLP profiles and sequencing of the ITS region revealed that, in addition to the host group, the present population can be assigned to the "Argentina 2" group. Disease development and histopathology were investigated with glasshouse observations using tomato, pepper, sugar beet and potato seedlings exposed to nematode infection for 45 days at 28 ± 2°C. Histopathology of tomato roots confirmed that all immature stages and young females and males are migratory, whereas mature females are obligate sedentary endoparasites. Rather than syncytia, large regions of cortical necrosis and cavities were detected in tomato swellings infected by juveniles. However, syncytia were associated only with adult females. Large root galls, hyperplasia, abnormal proliferation of lateral roots and asymmetry of root structure were common anatomical changes induced by the nematode feeding in tomato roots.

Stunted growth of fall-sown sugar beets (Beta vulgaris) associated with high incidence of crownroot infections and large soil infestations by Ditylenchus dipsaci were observed at the end of the crop growing season in southern Spain by early June 2005. The largest proportion (75%) of the nematode life-stages in plant and soil was the fourth-stage juvenile. The large number (up to 3,750 nematodes per gram of fresh tissue) of D. dipsaci individuals and severe anatomical alterations observed in storage sugar beet roots suggest that the stem and bulb nematode is the causal agent of the impaired growth of sugar beets observed in commercial fields. Observed morphological traits of nematode specimens and results of specific polymerase chain reaction (PCR) and phylogenetic analyses confirmed that the population of D. dipsaci infecting sugar beet belongs to the normal (nongiant) biological type of the nematode. Results of host-range bioassays indicated that the population of D. dipsaci infecting sugar beet in southern Spain reproduces on pea (including seeds and pods), onion, potato, spinach, and tomato, but not on bean, cotton, maize, and tobacco. These results indicate that D. dipsaci may be an important constraint for sugar beet crops in the affected area, but also for other important crops commonly used in rotation with them.

Stunted growth of fall-sown sugar beets (Beta vulgaris) associated with high incidence of crownroot infections and large soil infestations by Ditylenchus dipsaci were observed at the end of the crop growing season in southern Spain. The largest proportion (75%) of the nematode life-stages in plant and soil was the fourth-stage juvenile. The large number (up to 3,750 nematodes per gram of fresh tissue) of D. dipsaci individuals and severe anatomical alterations observed in storage sugar beet roots suggest that the stem and bulb nematode is the causal agent of the impaired growth of sugar beets observed in commercial fields. Observed morphological traits of nematode specimens and results of specific polymerase chain reaction (PCR) and phylogenetic analyses confirmed that the population of D. dipsaci infecting sugar beet belongs to the normal (nongiant) biological type of the nematode. Results of host-range bioassays indicated that the population of D. dipsaci infecting sugar beet in southern Spain reproduces on pea (including seeds and pods), onion, potato, spinach, and tomato, but not on bean, cotton, maize, and tobacco.

Root-knot nematodes (Meloidogyne spp.) are sedentary, obligate endoparasites in plants, where they induce specialized feeding sites. The feeding sites act as strong metabolic sinks to which photosynthates are mobilized. The histopathological modifications in the nematode-induced feeding sites of artificially inoculated chickpea cv. UC 27 were qualitatively and quantitatively compared using five isolates of M. artiellia and one isolate each of M. arenaria, M. incognita, and M. javanica. All Meloidogyne isolates infected chickpea plants, but root gall thickening was significantly less for M. artiellia isolates than for the other Meloidogyne species. Nevertheless, neither the number of giant cells in the feeding site (averaging four to six) nor the area of individual giant cells was influenced by nematode species or isolate. However, the number of nuclei per giant cell was significantly smaller, and the maximum diameters of nuclei and nucleoli were significantly greater, in giant cells induced by M. artiellia isolates than in those induced by M. arenaria, M. incognita, or M. javanica. In a second experiment, M. artiellia-induced giant cells in faba bean and rapeseed also contained a small number of large nuclei.

8 pages, 5 figures.-- PMID: 18943038 [PubMed].-- Available Open Access at the publisher site., Root-knot nematodes (Meloidogyne spp.) are sedentary, obligate endoparasites in plants, where they induce specialized feeding sites. The feeding sites act as strong metabolic sinks to which photosynthates are mobilized. The histopathological modifications in the nematode-induced feeding sites of artificially inoculated chickpea cv. UC 27 were qualitatively and quantitatively compared using five isolates of M. artiellia and one isolate each of M. arenaria, M. incognita, and M. javanica. All Meloidogyne isolates infected chickpea plants, but root gall thickening was significantly less for M. artiellia isolates than for the other Meloidogyne species. Nevertheless, neither the number of giant cells in the feeding site (averaging four to six) nor the area of individual giant cells was influenced by nematode species or isolate. However, the number of nuclei per giant cell was significantly smaller, and the maximum diameters of nuclei and nucleoli were significantly greater, in giant cells induced by M. artiellia isolates than in those induced by M. arenaria, M. incognita, or M. javanica. In a second experiment, M. artiellia induced giant cells in faba bean and rapeseed also contained a small number of large nuclei., This research was supported by grant AGL2003-00640 from Comisión Interministerial de Ciencia y Tecnología (CICYT), Ministerio de Educación y Ciencia of Spain.

Host–parasite relationships in root-knot disease of spinach caused by Meloidogyne incognita race 1 were studied under glasshouse conditions. Nematode-induced mature galls were large and usually contained one or more females and egg masses with eggs. Feeding sites were characterized by the development of giant cells containing granular cytoplasm and many hypertrophied nuclei. The cytoplasm in these giant cells was aggregated alongside the thickened cell walls. Stelar tissues within galls appeared disorganized. The relationship between initial nematode population density (Pi) in a series from 0–128 eggs and second-stage juveniles per cm3 soil and growth of spinach cv. Symphony F1 seedlings was tested under glasshouse conditions. A Seinhorst model [y = m + (1 - m)zP–T] was fitted to fresh top- and total plant-weight data for inoculated and control plants. Tolerance limits (T) of spinach cv. Symphony F1 to M. incognita race 1 for fresh top and total plant weights were 0·25 and 0·5 eggs and second-stage juveniles per cm3 soil, respectively. The minimum relative values for fresh top and total plant weights were zero in both cases at Pi = 32 eggs and second-stage juveniles per cm3 soil. Root galling was least at low initial population densities and greatest at 16 eggs and second-stage juveniles per cm3 soil. Maximum nematode reproduction rate was 33·1-fold at the lowest Pi.

High infection rates of wild olive (Olea europaea sp. sylvestris) feeder roots and soil infestation by a new root-knot nematode were found in sandy soil at Vejer de la Frontera (Cádiz), southern Spain. Morphometric traits and analyses of the nematode esterase electrophoretic pattern as well as of the internal transcribed spacer 1 (ITS1)-5.8S gene and D2-D3 fragment of the 28S gene of rDNA showed that specimens differed clearly from known root-knot nematodes. Studies of host–parasite relationships showed a typical susceptible reaction in naturally infected wild olive plants and in olive planting stocks (cvs. Arbequina and Picual) artificially inoculated with the nematode. However, the nematode did not reproduce in artificially inoculated chickpea, pea, and tomato. Because of the ability of this new nematode to infect wild and cultivated olives only, we suggest the common name, "Mediterranean olive root-knot nematode". The species is herein described and illustrated, and named as Meloidogyne baetica n. sp. The new root-knot nematode can be distinguished from other Meloidogyne spp. by (i) the perineal pattern, which is almost similar to that of M. artiellia, characterized by distinct inner striae forming two distinct longitudinal bands, extending throughout the perineum to just below the vulva; (ii) female excretory pore anterior to the level of stylet knobs, excretory pore distance from anterior end/length of stylet ratio extremely small (0.5 to 0.8); and (iii) second-stage juveniles with elongate-conoid tail. Phylogenetic trees derived from maximum parsimony analyses showed that M. baetica is closely related to M. artiellia, the cereal and legume root-knot nematode., Research was supported in part by a Bilateral Research Program funded by Consejo Superior de Investigaciones Científicas (CSIC), Spain, and Consiglio Nazionale delle Ricerche (CNR), Italy.

Radophulus similis, the burrowing nematode colonizes and reproduces in roots and rhizomes of Anthurium andraeanum Linden ex Andre in Madeira, Portugal. Histological examinations of infected rhizomes shows necrosis and cavities extending from the cortical parenchima into the vascular bundles. All nematode life stages occurred in the phloem. Nematode specimens were also observed in the metaxylem elements.

Severe infections of white mulberry feeder roots and heavy soil infestations by Meloidogyne arenaria race 2 were found in southern Spain. This is the first record of M. arenaria on white mulberry in Europe. Morphometric observations, analysis of the esterase electrophoretic pattern, and artificial inoculations of race differentials were used to characterize nematodes. Nematode-induced mature galls were spherical and usually contained one or more females, males, and egg masses with eggs. Feeding sites were characterized by the development of giant cells that contained granular cytoplasm and many hypertrophied nuclei. Giant cell cytoplasm was aggregated along a thickened cell wall. Vascular tissues within galls appeared disorganized. The relationship between the initial nematode population density (Pi) in a series from 0 to 1,024 eggs and juveniles/cm3 soil and growth of white mulberry seedlings was tested in the greenhouse. A Seinhorst model was fitted to plant height and top fresh weight. Tolerance limits of white mulberry to M. arenaria race 2 for plant height and top fresh weight were, respectively, 1.1 and 1.38 eggs and juveniles/cm3 soil. The minimum relative values for plant height and top fresh weight were 0 at Pi e 64 and Pi e 128 eggs and juveniles/cm3 soil, respectively. Maximum nematode reproduction rate was 435-fold at the lowest Pi.

Rotylenchus laurentinus was found on the roots of carrots (Daucus carota L.) growing in sandy soils along the south Adriatic coast of Italy. The original description is amplified and supplemented with scanning electron microscope (SEM) observations. Much of the cuticle has a characteristic 'tiled' appearance and the male head is much 'squarer' than that of the female. R. laurentinus is semi-endoparasitic on the feeder roots of carrots and causes lesions and cavities in epidermal and cortical tissues.

High infection rates of European sea rocket feeder roots by an unknown root-knot nematode were found in a coastal dune soil at Cullera (Valencia) in central eastern Spain. Morphometry, esterase and malate dehydrogenase electrophoretic phenotypes and phylogenetic trees demonstrated that this nematode species differs clearly from other previously described root-knot nematodes. Studies of host-parasite relationships showed a typical susceptible reaction in naturally infected European sea rocket plants and in artificially inoculated tomato (cv. Roma) and chickpea (cv. UC 27) plants. The species is herein described and illustrated and named as Meloidogyne dunensis n. sp. The new root-knot nematode can be distinguished from other Meloidogyne spp. by: (i) perineal pattern rounded-oval, formed of numerous fine dorsal and ventral cuticle striae and ridges, lateral fields clearly visible; (ii) female excretory pore at the level of stylet knobs, EP/ST ratio 1.6; (iii) second-stage juveniles with hemizonid located 1 to 2 annuli anteriorly to excretory pore and long, narrow, tapering tail; and (iv) males with lateral fields composed of four incisures anteriorly and posteriorly, while six distinct incisures are observed for large part at mid-body. Phylogenetic trees derived from distance and maximum parsimony analyses based on 18S, ITS1-5.8S-ITS2 and D2-D3 of 28S rDNA showed that M. dunensis n. sp. can be differentiated from all described root-knot nematode species, and it is clearly separated from other species with resemblance in morphology, such as M. duytsi, M. maritima, M. mayaguensis and M. minor.

During a nematode survey, severe infections of tobacco feeder roots and heavy soil infestations by Meloidogyne incognita race 1 were found in S. Miguel (Azores islands, Portugal). This is thought to be the first record of M. incognita infection of tobacco in Azores. The morphology of various life stages, analysis of the esterase electrophoretic pattern and differential host tests were used for nematode characterization and identification. Nematode-induced mature galls were spherical and/or ellipsoidal and usually contained more than one female, males and egg masses with eggs. Feeding sites were characterized by the development of giant cells that contained granular cytoplasm and many hypertrophied nuclei. Giant cell cytoplasm was aggregated along a thickened cell wall. Vascular tissues within galls appeared disorganized. The relationship between the initial nematode population density and growth of tobacco plants was tested in a glasshouse experiment in which inoculum levels varied from 0 to 512 eggs and juveniles (J2) cm-3 of the soil. Seinhorst's model was fitted to height and top fresh weight data of the inoculated and control plants. Tolerance limits with respect to plant height and fresh top weight of tobacco cv. Erzegovina plants to M. incognita race 1 were estimated as 1.25 eggs and J2 cm-3 of the soil. The maximum nematode reproduction rate was 404.7 at an initial population density of 4 eggs and J2 cm-3 of the soil.