Thermal requirements for the embryonic development and life cycle of Meloidogyne hispanica

The life cycle of a Portuguese Meloidogyne hispanica isolate on susceptible cv. Easypeel and resistant (Mi‐1.2 gene) cv. Rossol tomato plants was studied in growth chambers at constant temperatures (10–35°C). The development within the egg and hatching were compared to those of a Portuguese M. arenaria isolate. The base temperature was 10·11 and 8·31°C with 179·5 and 235·3 thermal units for M. hispanica and M. arenaria, respectively, suggesting better potential adaptation to low temperatures by M. arenaria than M. hispanica. No egg development occurred at 10 or 35°C. An increase in invasion of tomato roots by M. hispanica second‐stage juveniles (J2s) was correlated with an increase in temperature on both tomato cultivars. Tomato cv. Rossol limited M. hispanica development at 20, 25 and 30°C, but not at 35°C, indicating that these high temperatures blocked the resistance mechanism provided by the Mi‐1.2 gene. At 15°C, J2s penetrated tomato cv. Rossol roots, but failed to develop and establish feeding sites. On tomato cv. Easypeel, nematode development and reproduction occurred at 20, 25 and 30°C, but at 20°C the life cycle was 1·5 and 2·0 times longer than at 25 and 30°C, respectively. No egg production was observed at 15°C. The results of this study showed that M. hispanica is most suited to soil temperatures around 25°C. Predicted climate change might favour the spread of this nematode species into southern Europe and northwards. The thermal requirements for M. hispanica development are analysed and compared with those of M. arenaria, M. hapla, M. incognita and M. javanica.     

Does soil warming affect the interaction between Pasteuria penetrans and Meloidogyne javanica in tomato plants?

A system to grow tomato plants infected by Meloidogyne javanica under constant temperatures of 18, 21, 24, 27 and 30 °C was developed and used to assess how temperature and the application of the biological control bacterium Pasteuria penetrans affected plant growth, the nematode population and endospore production. Each plant was inoculated with 300 second‐stage juveniles (J2) with four or five spores of P. penetrans attached to their cuticles or with 300 nematodes without P. penetrans. Increasing soil temperature increased tomato growth, the number of endospores per female, and the number of galls of M. javanica at the end of 38 days. Increasing temperatures up to 27 °C also increased the number of egg masses produced by M. javanica. Presence of P. penetrans reduced the numbers of galls and egg masses at all temperatures by up to 52.2% and 61.4% at 27 and 30 °C, respectively. Pasteuria penetrans reduced the M. javanica population even at soil temperatures of 18 and 21 °C. However, temperatures of 27 and 30 °C enhanced nematode control and the production of P. penetrans endospores is faster. The system developed in this work is simple and efficient for growing plants under constant temperatures and can be used for different purposes.     

Assessing risks of pine wood nematode Bursaphelenchus xylophilus transfer between wood packaging by simulating assembled pallets in service

The risks of Bursaphelenchus xylophilus (pine wood nematode) transfer in relation to wood material were assessed. Combinations of infested and non‐infested adjacent boards, long‐blocks and blocks of Pinus pinaster, simulating assembled pallets, were assessed. For the recipient wood, pieces with natural moisture content (MC), heat‐treatment (56°C for 30 min in the core) and kiln‐drying to <20% MC were tested, along with in‐service boards from pallets. Donor and recipient wood materials were kept in direct contact at 25°C or 10°C, with nine replicates per treatment. Bursaphelenchus xylophilus was found to transfer rapidly at 25°C when the wood had an MC above fibre‐saturation point (>30%). Nematode reproduction was rapid and sustained, gradually declining to zero at 40 weeks. Bursaphelenchus xylophilus did not transfer to kiln‐dried or to in‐service wood with an MC below fibre‐saturation point, or to wood at 10°C. The key factors determining nematode transfer were the ambient temperature, the nematode load of the donor wood and the MC of the recipient wood, with a ‘barrier’ of 20% MC below which it becomes unsuitable for nematode transfer. This finding indicates that there is a limited risk of spread of B. xylophilus in treated and untreated solid wood packaging materials.     

Germination and seedling emergence of glyphosate‐resistant and susceptible biotypes of goosegrass (Eleusine indica[L.] Gaertn.)

Effects of environmental factors on the germination and seedling emergence of glyphosate‐resistant (R) and ‐susceptible (S) biotypes of Eleusine indica (L.) Gaertn. were examined under laboratory and greenhouse conditions. The R biotype exhibited a higher germination percentage compared with the S biotype at constant temperatures of 20 and 35°C under dark conditions, and alternating temperatures of 30/25°C, and 35/25°C during a 12 h photo period. For both biotypes, germination was optimal at alternating temperatures of 30/20°C and 35/20°C. However, there was no significant difference (P > 0.05) in the germination between the R and S biotypes at these temperature regimes. The germination of both biotypes was inhibited by osmotic stress imposed by a water potential of ?0.80 MPa. When the moisture stress was released and the seeds were subsequently transferred to distilled water, the germination was enhanced to approximately 90% and 16% for the R and S biotype seeds, respectively. Higher emergence rates were obtained in shallow seed depths (0 or 2 cm) compared to deep depths. Emergence percentage of the R biotype was higher than that of the S biotype at 0 cm and 2 cm depths. The maximum emergence percentage of the R biotype was higher than that of S biotype when seeds were sown on the surface of either loamy or clay loam soil taken from three different sites.     

Effects of temperature on infection and subsequent development of clubroot under controlled conditions

Controlled‐environment studies were conducted on two Brassica crops (canola, Brassica napus; and Shanghai pak choi, B. rapa subsp. chinensis var. communis) to examine the effects of temperature on infection and subsequent development of clubroot caused by Plasmodiophora brassicae. In the first experiment, canola seedlings were grown in infested soil for 3 weeks at 14–26°C to assess the impact on primary and secondary infection and transferred to 20°C for 3 weeks to assess symptom development under uniform conditions, or started at 20°C for 3 weeks and then placed at the treatment temperatures for the final 3 weeks to assess the impact of temperature on symptom development. A second experiment examined a wider range of temperatures (10–30°C). Similar experiments were also conducted on Shanghai pak choi. The studies demonstrated that clubroot severity was affected by temperature during both infection and vegetative development of the crop. Both early and late in crop development, little or no clubroot developed at temperatures at or below 17°C, and development was slower above 26°C than at 23–26°C for both crops throughout the study. In canola, the high levels of inoculum used in the study resulted in a high incidence of clubroot irrespective of temperature, but in pak choi incidence showed the same pattern as severity. This is the first study to demonstrate under controlled conditions that temperature during vegetative growth of the crop affects symptom development of clubroot.     

Temperature requirements for after-ripening in buried seeds of four summer annual weeds

Freshly matured, seeds of the four summer annuals Ambrosia artemisiifolia, Polygonum pensylvanicum, Amaranthus hybridus and Chenopodium album were buried in soil at (12/12 h) daily thermoperiods of 15/6, 20/10, 25/15, 30/15 and 35/20°C and at a constant temperature of 5°C. After 0, 1, 3 and 5 months, seeds of each species at each temperature were exhumed and tested at a 14-h daily photoperiod at all six temperatures. Fresh seeds of A. artemisiifolia and P. pensylvanicum did not germinate at any temperature, those of A, hybridus germinated to 4 and 64% at 30/15 and 35/20°C, respectively, and those of C. album to 11–20% at 25/15, 30/15 and 35/20°C. Seeds of A. artemisiifolia and P. pensylvanicum, which germinate only in spring, required exposure to low (5, 15/6°C) temperature to after-ripen completely (i.e., to gain the ability to germinate over a wide range of temperatures), and little or no after-ripening occurred at high (25/15, 30/15 and 35/20°C) temperatures. Seeds of A. hybridus and C. album, which germinate in spring and summer, required exposure to low temperature to after-ripen completely, but at high temperatures they rapidly gained the ability to germinate at high temperatures. Regardless of the burial temperatures and species, when after-ripening occurred, seeds firs germinated at high and then at low temperatures. The minimum germination temperature for a species decreased with after-ripening temperature and with an increase in the length of the burial period.     

Dormancy and viability of Phalaris minor seed in a rice–wheat cropping system

Seed placement, soil temperature and soil moisture content influenced the process of after-ripening in Phalaris minor seeds. Seeds of P. minor collected from the soil just after wheat harvesting exhibited higher germination than seeds from P. minor threshed directly. There was a pronounced impact of periodic inhabitation of seed into the soil on germination after its dispersal. Germination was strongly inhibited when the seed was kept in soil at more than field capacity (FC) or in water. Maximum germination of seed incubated in soil at FC occurred at 30°C while a temperature of 40°C favoured after-ripening of seed when mixed with dry soil or kept dry without any medium. Release from conditional dormancy was quicker in the seed retrieved from the soil kept at 20°C than at 10°C. Seed release from conditional dormancy and germination increased with a rise in temperature from 30 to 40°C when the seed was retrieved from incubation in soil at FC for 70 days. The seed kept immersed in water was least responsive to a rise in temperature. Seed recovered from dry soil, or kept without any medium, responded quickly at both temperatures. Light enhanced the germination of Phalaris minor seed. The seedbank subjected to rice (Oryza sativa) field management conditions lost vigour in comparison with the seed stored in laboratory. There was significant variability in seed viability when exposed to differential water management conditions in rice.     

Role of temperature in regulating timing of germination in soil seed reserves of Lamium purpureum L.

Fresh seeds of Lamium purpureum L. were dormant at maturity, and when buried and exposed to natural seasonal temperature changes they exhibited an annual dormancy/non-dormancy cycle. During burial in summer, fresh seeds and those that had been buried for 1 year afterripened and thus were non-dormant by September and October; light was required for germination. During autumn and winter seeds re-entered dormancy, and during the following summer they became non-dormant again. Dormant seeds afterripened when buried and stored over a range of temperatures, becoming conditionally dormant at low (5, 15/6°C) and non-dormant at high (20/10, 25/15, 30/15 and 35/20°C) temperatures. Conditionally dormant seeds germinated to high percentages at 5, 15/6 and 20/10°C, while non-dormant seeds germinated to high percentages additionally at 25/15, 30/15 and 35/20°C. Low temperatures caused non-dormant seeds to re-enter dormancy, while high temperatures caused a sharp decline in germination only at 30/15 and 5°C. The temperature responses of L. purpureum seeds are compared to those of L. amplexicaule L.     

A high temperature requirement for after ripening of imbibed dormant Poa annua L. seeds

Freshly harvested seeds of Poa annua L. collected in south Louisiana were stored in moist soil at seven temperatures between 5°C and 35°C. At monthly intervals, seed lots were removed and germinated at each of the seven temperatures. Seed were dormant for at least 1 month at all test temperatures. Seeds stored for 2 months at 30 and 35°C showed conditional dormancy; there was 100% germination at 10 or 15°C, and poorer germination at 5 or 20°C. Seeds started to lose viability after 2 months at 35°C and were dead after 7 months. In seeds stored at 10–30°C, there were increased percentages and a wider range of germination temperatures as storage time or storage temperatures increased. Seeds stored at 10°C remained dormant for 9 months, but by 12 months of storage the seeds germinated only at 5 or 10°C. Nearly all seeds stored at the same temperatures in air dry soil remained dormant for 6 months, regardless of storage temperature. These results differ from other reports of low temperatures breaking seed dormancy in Poa annua L. and suggest an adaptation to subtropical climates.     

Ecology of Xiphinema vuittenezi and Xiphinema pachtaicum in vineyards of north-east Croatia1

During a 3-year field study on two vineyards of north-eastern Croatia, the qualitative and quantitative composition as well as the vertical dynamics of Xiphinema spp. were determined each month. The greatest number of fertile X. vuittenezi females was noted in August-September at a soil moisture of 18–20%. The greatest number of larvae of this species was determined in September-October in a temperature range of 14–18°C and soil moisture of 18–22%. The development cycle of X. vuittenezi lasts about 24–33 months under natural conditions and that of its larval stages 3–8 months. The nematodes of this species are susceptible to high temperatures (above 20°C) and drought (under 13%). The greatest number of fertile females of X. pachtaicum was determined in July at a soil temperature of 20–24°C, absolute soil moisture of 16–20%. The greatest number of larvae was noted in September-October at a soil temperature of 16–21°C and soil moisture of 13–23%. The development cycle of X. pachtaicum in field conditions lasts about 12–13 months and that of the larval stages 2–3 months. This species demonstrated reduced activity at soil temperatures under 10°C and at soil moisture under 13%; larvae were less active than females at temperatures over 20°C. On the basis of the results obtained, it is suggested that sampling of vineyards to determine the distribution and population density of the two Xiphinema spp. should be performed at depths down to 50 cm in spring and autumn, which are also the most favourable times for nematicide application.     

Effect of temperature on primary infection by Plasmodiophora brassicae and initiation of clubroot symptoms

A study was conducted to assess the effect of temperature on infection and development of Plasmodiophora brassicae in root hairs of Shanghai pak choi (Brassica rapa subsp. chinensis) and on initiation of clubroot symptoms. Ten‐day‐old seedlings were grown in liquid‐sand culture, inoculated with resting spores and maintained in growth cabinets at 10, 15, 20, 25 and 30°C. Seedlings were harvested at 2‐day intervals, starting 2 days after inoculation (DAI) and continuing until swelling of the tap root was observed (maximum 28 days). Roots were assessed for root hair infection (RHI), stage of development of infection (primary plasmodia, zoosporangia, release of zoospores, secondary plasmodia), symptom development, and for clubroot severity at 24 DAI. Temperature affected every stage of clubroot development; RHI was highest and visual symptoms initiated earliest at 25°C, intermediate at 20 and 30°C, and lowest and latest at 15 and 10°C. Root hair infection was observed at every temperature, but clubroot symptoms developed only above 15°C. A substantial delay in the development of the pathogen was observed at 10 and 15°C. No symptoms were observed at 28 DAI in plants grown at 10°C. Swelling of the tap root was visible at 28 DAI in plants at 15°C, 14 DAI at 20 and 30°C, and 10 DAI at 25°C. These results support and explain the observation in companion studies that cool temperatures result in slower development of clubroot symptoms in brassica crops.     

Passive heat treatment of sweet basil crops suppresses white mould and grey mould

Sweet basil white mould (BWM, Sclerotinia sclerotiorum) and grey mould (BGM, Botrytis cinerea) are important diseases in Israel and other basil‐growing regions. The impact of microclimate on BWM and BGM and on plant sensitivity to these diseases was studied. Disease incidence was evaluated in three field experiments, each consisting of 10–12 polyethylene‐covered tunnels. BWM and BGM incidences were correlated with air temperature, relative humidity (RH) and soil temperature data. The incidence of BWM was negatively correlated with high (above >25 or >30 °C) air temperatures, RH > 50% and RH > 75% and high (>21 or >24 °C) soil temperatures. BGM incidence was negatively correlated with high (>25 °C) air temperatures and high (>21 or >24 °C) soil temperatures, and positively correlated with RH >65% or >75%. Shoots harvested from plants grown in the walk‐in tunnels were inoculated with S. sclerotiorum or B. cinerea under controlled conditions. Severity of BWM and BGM on those shoots was negatively correlated with tunnel air temperatures of >25 and >30 °C and soil temperatures >18 °C. Thus, high temperatures were related to reduced disease incidence and to reduced sensitivity to the pathogens. Experiments involving potted plants revealed that heating only the root zone suppresses canopy susceptibility to BWM and BGM. These findings indicate that the effect of high greenhouse temperatures involves an indirect systemic effect that renders the host less susceptible to disease. This effect was also observed in harvested shoots that were no longer at the high temperatures, and the effect was systemic.     

Seed germination, seedling establishment and growth patterns of wrinklegrass (Ischaemum rugosum Salisb.)

Several laboratory and glasshouse experiments were conducted to assess seed germination, seedling establishment and growth patterns of wrinklegrass (Ischaemum rugosum Salisb.) influenced by temperature and light regimes, and chemical media. Wrinklegrass was a positively photoblastic species, and seed germination was temperature‐dependent and light‐mediated. Seeds soaked in distilled water for 24 h, or oven‐dried at the respective temperature regimes of 15, 20, 25, 30, 35, or 40°C prior to treatment in distilled water and incubated in darkness, failed to germinate. Likewise, no germination prevailed when the seeds were exposed to similar temperature regimes and treated with 0.2 m KNO₃, 5% H₂O₂ or 0.01 m HNO₃, and incubated under continuous darkness. Seeds treated with 5% H₂O₂ at 30°C, or oven‐dried and treated with 0.01% M HNO₃ at 35°C registered 10 and 20% germination. Approximately 75 and 90% of the light‐exposed seeds for all treatments germinated in the first three and six days at 25°C. No germination occurred at 15°C in the first three days after treatment. Seeds subjected to 40°C for six days after treatment recorded 36% germination. The optimum temperatures for seed germination were 25–30°C. Seed drying and soaking treatments widened the windows of the optimal temperatures for wrinklegrass germination. The acidic media of KNO₃, H₂O₂ or HNO₃ favored seed germination. Less than 5% of seed germination occurred with burial or water inundation at depths exceeding 2 cm. Seed burial or inundation at ≥2 cm depths inhibited seed germination. Seeds sown onto moist paddy soils registered ca. 50% germination. Free‐floating seeds on the water surface registered ca. 98% germination within the first six days after seeding. The mean number of seedlings that survived was inversely proportional to water depths, with close to 100% mortality at the 14 cm depths of inundation. Both plant height and seedling survival were linearly proportional to the amount of root mass of seedlings which penetrated the soil. The weed was a prolific seed producer (ca. 6000 seeds/genet or 18 000 seeds/genet per year). The vegetative and reproductive efforts of each wrinklegrass plant registered values of 0.68 and 0.32, respectively.     

Weight loss in overwintering below‐ground parts of Sonchus arvensis under current and temperature‐elevated climate scenarios in Sweden

Weight loss in overwintering below‐ground parts of perennial weeds has been attributed to respiration, but neither its temperature dependence nor its relevance for biomass dynamics under changing climate conditions have been investigated. In two experiments, we quantified weight loss of the perennial weed Sonchus arvensis, by measuring weight changes over time of sprouting roots in dark rooms at temperatures of 4, 8 and 18°C. Dry weight loss rates were 0.47, 0.64 and 1.47% day^?1 at 4, 8 and 18°C, respectively, giving a half‐life time of 149, 110 and 47 days, respectively. A factor by which weight loss rates increase for every 10° rise in temperature (Q₁₀) was equal to about 2.3. Cumulative weight loss may comprise >40% of the below‐ground biomass during overwintering periods. Applying weight loss rates and Q₁₀ to elevated soil temperature projections showed that losses during winter seasons in central Sweden will remain basically constant, the effect of increased weight loss at higher temperatures being balanced by shorter winters. This implies that need for control of S. arvensis in a changing climate will persist, but that shorter winter seasons will provide a longer time window for control of S. arvensis prior to sowing crops.     

Low root‐to‐root transmission of a tobamovirus,yellow tailflower mild mottle virus,and resilience of its virions

Tobamoviruses are serious pathogens because they have extremely stable virions, they are transmitted by contact, and they often induce severe disease in crops. Knowledge of the routes of transmission and resilience of tobamovirus virions is essential in understanding the epidemiology of this group of viruses. Here, an isolate of the tobamovirus yellow tailflower mild mottle virus (YTMMV) was used to examine root‐to‐root transmission in soil and in a hydroponic growth environment. Root‐to‐root transmission occurred rarely, and when it occurred plants did not exhibit systemic movement of the virus from the roots to the shoots over a 30‐day period. The resilience of YTMMV virions was tested in dried leaf tissue over time periods from one hour to one year under temperatures ranging from ?80 to 160 °C. Infectivity was maintained for at least a year when incubated at ?80 or 22 °C, or at fluctuating ambient temperatures of 0.8 to 44.4 °C, but incubation under dry conditions at 160 °C for >4 days eliminated infectivity. Exposure of virions to 0.1 m sodium hydroxide or 20% w/v skimmed milk solution for 30 min, treatments recommended for tobamovirus inactivation, did not abolish infectivity of YTMMV.     

Comparative biology and life table of Habrobracon hebetor (Hymenoptera: Braconidae) on Anagasta kuehniella (Lepidoptera: Pyralidae) at five constant temperatures

Habrobracon hebetor Say is an ectoparasitoid that has been used as a control agent of various lepidopteran pests. Temperature-dependent life table and thermal characteristics of H. hebetor are important in understanding the dynamics of host–parasitoid relationships and for optimizing biocontrol programmes. The influence of five constant temperatures (15, 20, 25, 30 and 35 °C) on the biology of H. hebetor when parasitizing Anagasta kuehniella Zeller was studied. The survival rate of immature stages increased from 16.67% to 83.81% as temperature increased from 15 to 30 °C and then decreased at 35 °C. Total development time ranged from 45.70 days at 15 °C to 7.10 days at 35 °C. The lower temperature threshold for immature stages varied slightly around a value of 11–12 °C. The net reproductive rate (R₀) values were significantly different among temperatures and the highest value was found at 30 °C (85.10). The high survival rate and net reproductive rate combined with a relatively short generation time at 30 °C resulted in the intrinsic rate of increase (r_m) being highest (0.312 d^?1) at this temperature. Considering the acquired results, the temperature range between 25 and 30 °C was optimal for H. hebetor.     

The solar chamber: an innovative technique for controlling verticillium wilt of olive1

Control of olive tree wilt, caused by Verticillium dahliae, is not easy. A simple solar-chamber technique has been developed to achieve effective control. The treated tree is irrigated, the soil is covered by a plastic sheet, and a chamber made of a metal framework covered with plastic sheets is placed over the tree. Trees were exposed for 10, 15 and 20 days. Using this approach the temperature in the chamber reached 55°, and soil temperatures at 5 and 15 cm depth reached 55 and 45°, respectively. It was no longer possible to isolate V. dahliae from infected trees after 15–20 days. Growth of treated trees was improved as compared with the untreated ones. Laboratory studies on the efficacy of dry heat on the survival of V. dahliae in diseased branches showed that 50–55°C was lethal after 1 h. On PDA medium, the fungus was killed in 1 h at 50°C and in 45 min at 55°C.     

Effect of temperature during burial on dormant and non-dormant seeds of Lamium amplexicaule L. and ecological implications

Spring-produced seeds of Lamium amplexicaule L. were dormant at maturity in May and after-ripened when buried and stored over a range of temperatures, becoming conditionally dormant at low (5, 15/6 and 20/10°C) and non-dormant at high (25/15, 30/15 and 35/20°C) temperatures. Conditionally dormant seeds germinated to high percentages at 5 and 15/6°C, and non-dormant seeds germinated to high percentages at 5, 15/6, 20/10, 25/15 and 30/15°C. Seeds that became conditionally dormant at 5°C afterripened completely (i.e. became non-dormant) after transfer to 30/15°C. Buried seeds that became non-dormant in a non-temperature-controlled glasshouse during summer were still non-dormant after 12 weeks of storage at 30/15°C, while those stored at 5°C for 12 weeks had entered conditional dormancy. Thus, low temperatures cause reversal of the afterripening that takes place at high temperatures, but not that which takes place both at low and at high temperatures. Low winter temperatures cause dormant autumn-produced seeds and non-dormant seeds in the soil seed pool to become conditionally dormant. The ecological consequences of these responses to temperature are discussed in relation to the timing of seed germination in nature.     

Seed dormancy and periodicity of seedling emergence in Veronica hederifolia L.

Emergence of Veronica hederifolia seedlings began in mid-October and continued into spring; few appeared from June to September. Ripe seeds shed in June were dormant but wben buried in soil outdoors developed a capacity for germination initially at low temperatures (constant4 C; daily alternations of 4-10° and 4-1 5 C) and later at somewhat higher temperatures, with peak germination in September-November. During winter, spring and early summer thc germination capacity declined, to increase again in late summer and early autumn. Cyclic physiological changes thus occur in seeds of V,hederifolia present in the soil, with which lhe consistent seasonal periodicity of seedling emergence is associated. In dry storage ihe capacity for germination progressively increased, but alter 12 months there was a sharp decline in germination at 4° C. Few seeds germinated at 20° C, but moistening with GA 4/7; brought about complete germination at this temperature.     

Spatial and temporal dynamics of Meloidogyne minor on creeping bentgrass in golf greens

Meloidogyne minor, first reported on potatoes in the Netherlands in 2004, is an emerging nematode pest in Europe. It damages turfgrass, particularly creeping bentgrass (Agrostis stolonifera) grown on sandy soils such as those of golf greens. However, little is known of the nematode's life history and pathology. In this study, the spatial and temporal distribution of M. minor on a creeping bentgrass green in Ireland was determined over a 15 month period. Cores were taken on transects across yellowing patches of grass caused by nematode damage. Second‐stage juveniles (J2) were absent from the soil from November to February, when soil temperatures were below 10°C. Both galls and egg masses were present throughout the year but were more abundant in late summer and early autumn. More J2, galls and egg masses were present in the top 10 cm of soil than at a depth of 11–20 cm. The nematode population tended to decrease as distance from the centre of the yellow patches increased. The diameter of visual symptoms (yellow patches) was also recorded over the 15 months. The mean diameter of five sampled patches increased from 23·7 cm in June 2003 to 45·2 cm in August 2004. There were 158–193 galls per 100 cm³ soil at the margin of the visible infested area, indicating that this could be the threshold level for visible symptoms.