Transmission of prunus necrotic ringspot virus using plum pollen and thrips

Prunus necrotic ringspot virus (PNRSV) was transmitted to cucumber but not to peach seedlings after they were dusted with infective plum pollen and caged with 8–10 thrips per seedling for 24 h. When the pollen was taken from three plum trees shown by mechanical inoculation tests to have highly infective flower buds and pollen, the transmission rates to cucumber seedlings were 56% with Thrips tabaci and 66% with a mixture of five thrips species collected from Ageratum houstonianum flowers. However, the transmission rate averaged only 7% when pollen was taken from five other plum trees which had flowers with less infectivity in sap transmission tests. In 1990 T. imaginis, T. tabaci and T. australis, which were present in the mixture of thrips from A. houstonianum, also formed the major part of the thrips population in flowers of the plum trees used as the pollen source.     

The coincidence of thrips and dispersed pollen in PNRSV-infected stonefruit orchards – a precondition for thrips-mediated transmission via infected pollen

Recent laboratory studies have demonstrated that Prunus necrotic ringspot virus (PNRSV) (family Bromoviridae) can be readily transmitted when thrips and virus‐bearing pollen are placed together on to test plants. For this transmission mechanism to result in stonefruit tree infection in the field, PNRSVbearing pollen must be deposited onto surfaces of stonefruit trees on which thrips also occur. In a previous paper, we demonstrated that almost all pollen in a PNRSV‐infected Japanese plum orchard in southeastern Queensland was deposited onto flowers, whereas few grains occurred on leaves and none on stems. Here, we present results of our investigation of thrips species composition, distribution and abundance on stonefruit trees in the same study area as our previous pollen deposition study. We collected a total of 2010 adult thrips from 13 orchards during the 1989, 1991 and 1992 flowering seasons of which all but 14 were in the suborder Terebrantia. Most (97.4%) terebrantian thrips were of three species, Thrips imaginis, Thrips australis and Thrips tabaci. Thrips tabaci as well as species mixtures that included T. imaginis, T. australis and T. tabaci have been shown to transmit PNRSV via infected pollen in laboratory tests. Adult thrips were frequently collected from flowers but rarely from leaves and never from stems. Large and significant differences in numbers of T. imaginis, T. australis and T. tabaci adults in flowers occurred among orchards and between seasons. No factor was conclusively related to thrips numbers but flowers of late‐flowering stonefruit varieties tended to hold more thrips than those of early‐flowering varieties. Our results indicate that the common thrips species present on stonefruit trees in the Granite Belt are also ones previously shown to transmit PNRSV via infected pollen in the laboratory and that these thrips are concentrated in tonefruit flowers where most stonefruit pollen is deposited. These results contribute to mounting circumstantial evidence that stonefruit flowers may be inoculated with PNRSV via an interaction of thrips with virus‐bearing pollen and that this transmission mechanism may be an important cause of new tree infections in the field     

Host range, purification and properties of potato virus T

Potato virus T (PVT) infected nine species of tuber-bearing Solanum, most of them symptomlessly, and as a rule was transmitted through the tubers to progeny plants: two genotypes of S. tuberosum ssp. andigena were not infected. The virus was also transmitted by inoculation with sap to 37 other species in eight plant families. Chenopodium amaranticolor is useful as an indicator host, C quinoa as a source of virus for purification, and Phaseolus vulgaris as a local-lesion assay host; the systemic symptoms in Datura stramonium, Nicotiana debneyi and in these three species are useful for diagnosis. Attempts to transmit PVT by aphids failed, but the virus was transmitted through seed to progeny seedlings of four solanaceous species, and from pollen to seed of S. demissum. PVT was purified by clarifying sap with n-butanol or bentonite, followed by precipitation with polyethylene glycol, differential centrifugation and sedimentation in a sucrose density gradient. Purified preparations had an E260/E280 ratio of 1.18 and contained a single infective component with a sedimentation coefficient of 99 S. This component consisted of flexuous filamentous particles of about 640 times 12 nm that showed a characteristic substructure when stained with uranyl acetate. The virus particles contained a single species of infective single-stranded RNA, of molecular weight 2–2 times 106 daltons, and a single species of polypeptide of molecular weight about 27 000 daltons. PVT is serologically related to apple stem grooving virus but not to four other common potato viruses with flexuous filamentous particles. Apple stem grooving virus and PVT cause similar symptoms in several hosts, but also differ somewhat in host range and symptomatology. Apple stem grooving virus did not infect potato, caused additional symptoms in C. quinoa also infected with PVT, and its particles did not show the structural features specific to PVT. The two viruses are considered to be distinct. The cryptogram of PVT is R/1:2–2/(5): E/E: S/C.     

Transmission of Three Strains of Tobacco Streak Ilarvirus by Different Thrips Species Using Virus-infected Pollen

When cucumber seedlings were dusted with tobacco streak ilarvirus (TSV)-infected pollen and infested with 5–10 thrips (adults and larvae mixed), Thrips tabaci transmitted all three Australian strains of TSV. In similar work, Microcephalothrips abdominalis transmitted both and Frankliniella schultzei one strain, respectively, of two TSV strains tested. Transmission of the Ageratum strain (TSV-Ag) infecting pollen of Ageratum houstonianum was very efficient (100%) by all three thrips species. However, transmission rates of only 0–28% were achieved using the Ajuga strain (TSV-A) and the strawberry strain (TSVS) in pollen of other hosts. A fourth thrips species, T. parvispinus , transmitted TSV-Ag from infected tomato pollen to Chenopodium amaranticolor seedlings. There was, therefore, little or no vector specificity in the thrips transmission of the three strains of TSV, but factors associated with the virus-infected pollen affected the efficiency of transmission. This is the first report of F. schultzei and T. parvispinus as vectors of TSV.     

Preference of the vector thrips Frankliniella occidentalis for plants infected with thrips‐non‐transmissible Tomato spotted wilt virus

The effect of a thrips‐non‐transmissible Tomato spotted wilt virus (TSWV) on insect–host interactions between thrips and Arabidopsis thaliana was analysed. A wild‐type TSWV virulent isolate and a TSWV isolate that induces mild symptoms on inoculated plants (TSWV‐Mo) were used in this study, and TSWV‐Mo isolate was obtained by single local lesion isolation using Petunia x hybrid after several passages on Nicotiana rustica plants. In transmission test, although wild‐type TSWV (TSWV‐wt) was transmitted by two thrips species (transmission ratio; Frankliniella occidentalis, 25%; Thrips tabaci, 10%; and T. palmi, 0%), none of the thrips transmitted TSWV‐Mo. Feeding damage by F. occidentalis in A. thaliana plants was more extensive on TSWV‐wt‐infected plants than on TSWV‐Mo‐infected plants, despite comparable preference. Among the markers of plant defences, salicylic acid‐regulated genes were upregulated threefold to sixfold by TSWV‐wt or TSWV‐Mo infection. In contrast, jasmonate‐regulated genes and jasmonate/ethylene‐regulated genes were not affected by the infections. Pull assays showed that adjacent TSWV‐Mo‐infected plants were preferred over uninfected plants. In conclusion, our results showed that the transmissibility by thrips of TSWV is not related to preference of vector thrips and suggested that TSWV‐Mo‐infected plants may be used as attractants for behaviour control of thrips.     

Coffee Ringspot Virus Vectored by Brevipalpus phoenicis (Acari: Tenuipalpidae) in Coffee

Coffee ringspot is characterized by conspicuous ringspot symptoms on leaves, berries, and less frequently on twigs. It is caused by coffee ringspot virus (CoRSV), a short, bacilliform virus (40 nm × 100–110 nm). The virus is not seed borne and is transmitted by Brevipalpus phoenicis (Geijskes). Transovarial transmission within the mite does not occur. CoRSV has been mechanically transmitted to Chenopodium amaranticolor Coste and Reynaud, C. quinoa Wildenow, Beta vulgaris L., and Alternanthera tenella Colla resulting in local lesions. Systemic infection within both C. amaranticolor and C. quinoa occurs. Virions are found in the nucleus or cytoplasm of infected cells, commonly associated with membranes. Occasionally, membrane bounded particles are found within the cisternae of the endoplasmic reticulum. A characteristic electron lucent, nuclear inclusion is commonly found in many infected cells. These cytopathic effects place CoRSV among the nuclear type of Brevipalpus-borne viruses. The disease has been reported in several Brazilian states (São Paulo, Paraná, Minas Gerais, and Federal District) and recently found in Costa Rica. A similar disease is known in the Philippines, but no information exists about its relationship to CoRSV. Coffee ringspot had no economical significance until recently when a large scale infection was reported in Minas Gerais that resulted in yield loss.     

Suppressing spread of Tomato spotted wilt virus by drenching infected source or healthy recipient plants with neonicotinoid insecticides to control thrips vectors

Field experiments were done to determine whether drenching plants with two systemically active neonicotinoid insecticides, thiamethoxam and imidacloprid, suppresses spread of Tomato spotted wilt virus (TSWV) by thrips vectors. Separate treatments to TSWV ‘infector’ tomato (source) and healthy lettuce (recipient) plants provided information on the relative importance of targeting control at virus acquisition by nymphs versus virus transmission to healthy plants by adults. Drenches were applied either to seedlings just before transplanting or to soil around plants. The thrips vectors recorded were Frankliniella occidentalis, F. schultzei and Thrips tabaci, but F. schultzei and T. tabaci predominated. Overall ratios of external to internal TSWV spread into and within plots without insecticide ranged from 1 : 2.3 to 1 : 2.8 between field experiments. Applying thiamethoxam as a soil drench to both young source plants and recipient seedling transplants suppressed TSWV incidence by 86%, while such application to either young source or recipient seedlings diminished incidence by 67–70%. When thiamethoxam was applied either as a soil drench to old source plants and concurrently as a seedling drench to recipient plants or as a seedling drench to recipient plants alone, incidence was suppressed by 65–73% and 54–73%, respectively. Thiamethoxam applied as a soil drench to old source plants diminished incidence by only 33% or not significantly. Imidacloprid applied either as a soil drench to old source plants and concurently as a seedling drench or as a seedling drench alone, suppressed TSWV incidence by 90–92% and 80% respectively. Although adult vector thrips and nymph numbers were low, fewer adults and/or nymphs were sometimes recorded due to insecticide application. Drenching healthy seedlings with neonicotinoid insecticides just before transplanting can be an effective chemical control measure to include in integrated disease management strategies to suppress TSWV epidemics in short‐duration crops like lettuce.     

Crimson clover latent virus - a newly recognised seed-borne virus infecting crimson clover (Trigolium incarnatum)

Crimson clover latent virus (CCLV) was detected in five seed lots of crimson clover (Trifolium incarnatum) from Europe and in one from the United States of America. Ninety-seven per cent of all crimson clover plants examined were found to be infected but were without symptoms. Keeping crimson clover plants at 32–38°C for 34 days failed to free them from CCLV. The virus was not transmitted by Myzus persicae, but was transmitted by inoculation of sap to Chenopodium album, C. amaranticolor and C. quinoa. Twenty-four other plant species from seven families were not infected. CCLV was best propagated in C. quinoa in which it caused stunting and systemic chlorosis. Sap from infected C. quinoa was infective after dilution to 10^-2 but not 10^-3, after 10 min at 60°C but not 65°C, and after 20 days at 20°C. In neutral phosphotungstate, CCLV had isometric particles c. 26 nm in diameter with a hexagonal profile. About 20 to 80 A_1cm,260 units of purified virus were obtained from 1 kg of infected C. quinoa or C. amaranticolor leaves by extraction in 0.5 M phosphate buffer, pH 7.5, containing 0.01 M ethylene diamine tetra-acetate and 0.4% 2–mercaptoethanol and clarification with chloroform-butanol followed by two precipitations with polyethylene glycol (mol. wt 6000) and several cycles of differential centrifugation. Purified virus sedimented as three components with sedimentation coefficients (s°_{20, w}) of 52S, 101S and 122S. The 101S and 122S components had buoyant densities in CsCl of 1.438 and 1.495 g/cm³ respectively. From these values the nucleic acid content of the 101S and 122S components was estimated to be 32–35% and 40–41% respectively. The virus contained a single protein with an estimated mol. wt of 52 000 and two single-stranded RNA species of estimated mol. wt 1.6 × 10⁶ and 2.2 × 10⁶. CCLV was serologically unrelated to 31 other morphologically similar viruses. Although its vector is unknown, CCLV seems to have affinities with nepoviruses. The cryptogram of CCLV is R/1:2.2/40–41 + 1.6132–35:S/S:S/*.     

Prey suitability of western flower thrips,Frankliniella occidentalis,and onion thrips,Thrips tabaci,for the predatory mite Amblyseius swirskii

Western flower thrips, Frankliniella occidentalis, and onion thrips, Thrips tabaci, are both important polyphagous pests of vegetables and ornamentals in greenhouses. Difficulties in biological control of these pests have prompted a search for new natural enemies. Most recently, the predatory mite Amblyseius swirskii has been commercialised as biological control agent of whiteflies and thrips. However, little is known about the suitability of thrips as prey for A. swirskii. We therefore assessed prey acceptance and life history of A. swirskii when feeding on F. occidentalis and T. tabaci at 25±1°C. Amblyseius swirskii juveniles preyed upon first larval instars of both F. occidentalis and T. tabaci but suffered from high mortality (67 and 78%). Developmental time (egg to adult) of A. swirskii was 7.8 days with either prey species. Adult A. swirskii females readily accepted first larval instars of both thrips species, which were attacked in <20 min on a leaf and <10 min in an artificial cage. Oviposition rates (0.92 and 0.99 eggs/female/day) and offspring sex ratios (63 and 70% females) were similar with F. occidentalis and T. tabaci as prey. Less than one-third of juveniles reaching adulthood and oviposition rates below one egg/female per day resulted in relatively low intrinsic rates of increase (r _m) (0.056 and 0.024 per day with F. occidentalis and T. tabaci, respectively). Altogether, our study suggests that the recently reported superiority of A. swirskii to the widely used Neoseiulus cucumeris in suppression of thrips is due to other traits than its population growth capacity with thrips as prey.     

Effects of virus genotype and temperature on seed transmission of nepoviruses

Transmission of different nepoviruses through chickweed (Stellaria media) seed was differently affected by ambient temperature during seed production. Raspberry ringspot and tomato black ring (Scottish isolate) viruses were similarly and frequently transmitted at 14 , 18 and 22 ^oC, whereas arabis mosaic virus was transmitted most frequently at 14 ^oC, and strawberry latent ringspot and tomato black ring (German isolate) viruses at 22 ^oC. When infected by seed-borne nepoviruses, seedlings of S. media and other species were symptomless at 15–25 ^oC, and the viruses were therefore detected by inoculating sap to Chenopodium quinoa indicator plants. However, typical symptoms of arabis mosaic and tomato black ring viruses were induced by growing Nicotiana tabacum, N. clevelandii and C. quinoa seedlings infected with seed-borne virus at 33–37 ^oC during the third and fourth weeks after sowing, preceded and followed by periods at 15–25 ^oC. The proportion of N. tabacum seedlings developing symptoms was the same as that of untreated seedlings yielding sap-transmissible virus. Seed transmissibility of pseudo-recombinant isolates of raspberry ringspot and tomato black ring viruses, containing RNA-i from one virus strain and RNA-2 from another strain, depended greatly on the transmissibility of the strain contributing RNA-i. The source of RNA-2 had an additional but smaller influence. The satellite RNA (RNA-3) of tomato black ring virus was seed-transmitted in S. media and its occurrence in cultures did not affect the frequency of transmission of the virus. Results of testing the infectivity of extracts of seed from infected mother plants suggested that failure of seed transmission reflected failure to become established in the seed, not subsequent inactivation. Whereas seed transmissibility of raspberry ringspot virus is primarily dependent on information carried in RNA-i, transmissibility by nematode vectors, another property of major ecological importance, is determined by RNA-2. In the field, selection pressures presumably can act independently on the two parts of the genome but evidence was also obtained of selection for mutual compatibility of RNA-i and RNA-2.     

Specific Insect-Virus Interactions Are Responsible for Variation in Competency of Different Thrips tabaci Isolines to Transmit Different Tomato Spotted Wilt Virus Isolates

Local adaptation between sympatric host and parasite populations driven by vector genetics appears to be a factor that influences dynamics of disease epidemics and evolution of insect-vectored viruses. Although T. tabaci is the primary vector of Tomato spotted wilt virus (TSWV) in some areas of the world, it is not an important vector of this economically important plant virus in many areas where it occurs. Previous studies suggest that genetic variation of thrips populations, virus isolates, or both are important factors underlying the localized importance of this species as a vector of TSWV. This study was undertaken to quantify variation in transmissibility of TSWV isolates by T. tabaci, in the ability of T. tabaci to transmit isolates of TSWV, and to examine the possibility that genetic interactions and local adaptation contribute to the localized nature of this species as a vector of TSWV. Isofemale lines of Thrips tabaci from multiple locations were tested for their ability to transmit multiple TSWV isolates collected at the same and different locations as the thrips. Results revealed that the probability of an isofemale line transmitting TSWV varied among virus isolates, and the probability of an isolate being transmitted varied among isofemale lines. These results indicate that the interaction of T. tabaci and TSWV isolate genetic determinants underlie successful transmission of TSWV by T. tabaci. Further analysis revealed sympatric vector-virus pairing resulted in higher transmission than allopatric pairing, which suggests that local adaptation is occurring between T. tabaci and TSWV isolates.     

Effect of Fungicides on the Viability of Phylophthora cactorum Propagules m the Soil

Vein-clearing followed by downward rolling and necrosis of leaves and severe stunting of groundnut (Arachis hypogaea) plants were caused by cowpea mild mottle virus (CMMV). The virus was readily transmitted by mechanical sap inoculations to groundnut and to 10 plant species belonging to Leguminosae, Chenopodiaceae and Solanaceae. Chenopodium quinoa and Beta vulgaris were good diagnostic hosts. Diseased sap remained infective at 10^–3 but not 10^–4, when stored 8 to 9 days at 25 °C; for 10min at 75 °C but not 80°C. In limited tests, virus was not seed-transmitted m groundnut or soybean. Virus was transmitted by Bemisia tabaci but not by Aphis craccivora or Myzus persicae. An antiserum for CMMV was produced and virus was serologically related to CMMV reported on cowpea and groundnut crinkle virus (GCV) from West Africa. Employing carbon diffraction grating replica as a standard the modal length of virus particles to be 610 nm. Infected cells contained large number of virus particles associated with endoplasmic reticulum.     

Odour-baited traps influence thrips capture in proximal unbaited traps in the field

Two field experiments examined the distance over which an attractant odour of a volatile chemical could influence thrips capture in proximal traps that were without the odour. In each experiment a star‐shaped array of water traps consisted of a centre trap with or without an odour surrounded by odourless traps at 0.5, 1, 2, 5, and 10 m in eight equally spaced radial arms 45° apart. Experiments ran for 47 h (centre trap: ethyl nicotinate) or 7 h (centre trap: ethyl isonicotinate). Each had four replicates. With ethyl nicotinate, more thrips were trapped in the centre‐baited traps than in the unbaited centre traps (63×, 7×, 98× and 200× for total thrips, Thrips tabaci Lindeman ♀, and Thrips obscuratus Crawford ♀and ♂, respectively) (Thysanoptera: Thripidae). More total thrips and T. tabaci♀ were trapped in the centre traps baited with ethyl isonicotinate than in unbaited centre traps (21× for both). For ethyl nicotinate, numbers of T. obscuratus in unbaited traps downwind from the baited centre trap declined by 50% within 0.4 m (♀) and 2 m (♂) and by 95% within 3 m (both ♀ and ♂) based on model predictions. For ethyl isonicotinate, numbers of T. tabaci in unbaited traps downwind from the baited centre trap declined by 50% within 1.3 m and by 95% within 10 m based on model predictions. Wind direction was an important factor in the degree and direction of thrips capture with the highest thrips capture downwind from the centre trap with odour. There was no increase in numbers of T. tabaci in any traps without odour in the ethyl nicotinate‐centred array. Differences in trapping patterns between thrips species and odours indicated that there were thrips species–odour specific interactions. Experiments examining differences between traps with and without a thrips attractant odour need to be designed very carefully to ensure meaningful results especially in enclosed and/or low‐wind indoor situations.     

Ullucus virus C, a newly recognised comovirus infecting Ullucus tuberosus (Basellaceae)

Ullucus virus C (UVC) is a comovirus prevalent in Ullucus tuberosus grown at high altitudes in the Bolivian and Peruvian Andes. It was transmitted mechanically to U. tuberosus (Basellaceae) and to five of 26 species from three of eight other families, infecting U. tuberosus symptomlessly but inducing conspicuous systemic infection in Chenopodium amaranticolor and C. quinoa. Sap from infected C. quinoa was usually infective after 10 min at 70 but not 75 °C, after dilution to 10^-7 but not 10^-8, and after 8 but not 16 wk at 20 °C. UVC was not transmitted by either of two aphid species (Aphis gossypii and Myzus persicae) or through seed of C. quinoa, but it was transmitted by leaf contact between infected and healthy plants. UVC has isometric particles which, in neutral phosphotungstate, are c. 28 nm in diameter. The particles sediment as three components (T, M and B) with sedimentation coefficients (s^?_{20, w}) of 51 S (T), 95 S (M) and 116 S (B). M component particles have a buoyant density (g cm^-3) in caesium chloride of 1.404, and B component particles separated into minor and major sub-components with densities of 1.409 and 1.463, respectively. T, M and B particles were serologically indistinguishable, and each contained similar relative amounts of two polypeptides of mol. wts 20 700 and 45 100. T particles contained only protein, but M particles also contained c. 30% ss-RNA of mol. wt 1–45 ×10⁶ and B particles c. 38% ss-RNA of mol. wt 2·2 × 10⁶. The virus is serologically distantly related to cowpea mosaic virus but, as it showed no relationship to any of 11 other similar viruses, it is probably a distinct member of the comovirus group.     

Effects of single and dual species herbivory on the behavioral responses of three thrips species to cotton seedlings

This study investigated the olfactory responses of 3 thrips species [Frankliniella schultzei Trybom, F. occidentalis Pergrande and Thrips tabaci Lindeman (Thysanoptera: Thripidae)] to cotton seedlings [Gossypium hirsutum L. (Malvales: Malvaceae)] simultaneously damaged by different combinations of herbivores. Cotton seedlings were damaged by foliar feeding Tetranychus urticae Koch (Trombidiforms: Tetranychidae), Helicoverpa armigera Hübner (Lepidoptera: Noctuidae), Aphis gossypii Glover (Hemiptera: Aphididae) or root feeding Tenebrio molitor L. (Coleoptera: Tenebrionidae). Thrips responses to plants simultaneously damaged by 2 species of herbivore were additive and equivalent to the sum of the responses of thrips to plants damaged by single herbivore species feeding alone. For example, F. occidentalis was attracted to T. urticae damaged plants but more attracted to undamaged plants than to plants damaged by H. armigera. Plants simultaneously damaged by low densities of T. urticae and H. armigera repelled F. occidentalis but as T. urticae density increased relative to H. armigera density, F. occidentalis attraction to coinfested plants increased proportionally. Thrips tabaci did not discriminate between undamaged plants and plants damaged by H. armigera but were attracted to plants damaged by T. urticae alone or simultaneously damaged by T. urticae and H. armigera. Olfactometer assays showed that simultaneous feeding by 2 herbivores on a plant can affect predator–prey interactions. Attraction of F. occidentalis to plants damaged by its T. urticae prey was reduced when the plant was simultaneously damaged by H. armigera, T. molitor, or A. gossypii and F. schultzei was more attracted to plants simultaneously damaged by T. urticae and H. armigera than to plants damaged by T. urticae alone. We conclude that plant responses to feeding by 1 species of herbivore are affected by responses to feeding by other herbivores. These plant‐mediated interactions between herbivore complexes affect the behavioral responses of thrips which vary between species and are highly context dependent.     

Responses of Thrips tabaci to odours of herbivore‐induced cotton seedlings

Herbivore‐induced changes in plants have been widely viewed as defensive responses against further insect attack. However, changes in plants as a consequence of herbivore feeding can elicit various responses in herbivores; these are variable, context dependent, and often unpredictable. In this laboratory study, the responses of Thrips tabaci Lindeman (Thysanoptera: Thripidae) to volatiles emitted by intact and herbivore‐damaged or mechanically damaged cotton seedlings [Gossypium hirsutum L. (Malvaceae)] were investigated in dual‐choice olfactometer assays. Thrips tabaci showed increased attraction to seedlings subject to foliar mechanical damage and those with foliar damage inflicted by conspecifics or Tetranychus urticae Koch (Acari: Tetranychidae), upon which it preys. However, T. tabaci did not discriminate between intact seedlings and those with foliar damage inflicted by Helicoverpa armigera Hübner (Lepidoptera: Noctuidae), two other species of thrips, Frankliniella schultzei Trybom and Frankliniella occidentalis Pergrande (Thysanoptera: Thripidae), or those with root damage inflicted by Tenebrio molitor L. (Coleoptera: Tenebrionidae). Attraction of T. tabaci was also affected by herbivore density on damaged plants. That is, seedlings damaged by higher densities of T. urticae or T. tabaci were more attractive than seedlings damaged by lower densities of the corresponding arthropod. Although attracted to plants damaged by conspecifics or T. urticae, T. tabaci showed greater attraction to seedlings damaged by T. urticae than to seedlings damaged by conspecifics. Results are discussed in the context of the responses of F. schultzei and F. occidentalis to herbivore‐induced cotton seedlings, highlighting the complexity, variability, and unpredictability of the responses of even closely related species of insects to plants under herbivore attack.     

Population dynamics and integrated pest management of Thrips tabaci on leek under field conditions in northwest Italy

Thrips tabaci Lindeman (Thysanoptera: Thripidae) is a major pest of leek, Allium porrum L. (Alliaceae), in Piedmont, northwest Italy, and to control its infestation the leek crop is sprayed intensively with insecticides during the summer period. In order to find the most efficient and environment‐friendly method of thrips control, research was conducted on six commercial farms during 2005–2006 to assess thrips population composition and infestation levels, and in an experimental field during 2005–2007. Biological and chemical control were compared during 2005–2006, whereas integrated pest management was adopted during 2007. During the growing season, thrips and natural enemy populations were monitored at 14‐day intervals by beating plants; new leaves of plants were also visually inspected for thrips‐feeding symptoms. Furthermore, in the experimental field at harvest‐time, the level of thrips injury to plants was assigned to one of five classes, depending on the percentage of leaf area damaged. Over 99% of phytophagous adult thrips found were male and female T. tabaci. Infestations were very variable in the crops surveyed, partly due to broad‐spectrum chemical treatments against the leek pests, which often failed to control thrips. In general, populations peaked in September, when they reached the maximum mean values ranging between 1.7 and 33.1 thrips per plant. At harvest, none of the surveyed farms experienced quality losses due to thrips injuries. In the experimental field during 2005–2006, the mean number of thrips per plant was greater in the chemical than in the biological control treatment, even though damage indices showed no significant differences between the two treatments. Predatory thrips of the genus Aeolothrips (Thysanoptera: Thripidae) and predatory bugs of the genus Orius (Heteroptera: Anthocoridae), mostly Orius majusculus Reuter, were particularly abundant during 2007, supporting the importance of management with selective insecticides to encourage natural colonization by predators.     

Determination of soil depth inhabited by Frankliniella occidentalis (Pergande) and Thrips tabaci Lindeman (Thysan., Thripidae) under greenhouse cultivation

The objectives of this study were to determine the depth of penetration into the soil by Frankliniella occidentalis (Pergande) and Thrips tabaci Lindeman (Thysan., Thripidae) in cucumber and tomato crops in greenhouses. A metal sampling apparatus sampled for the two species of thrips at five levels of soil depth (0–10 cm), over seven dates of sampling, each in eight replications. In general, thrips were found to be in greater numbers in the first 2 cm of soil, with the number of insects decreasing with depth increasing. In the depth of 8–10 cm, no insects were found. Number of thrips found in the soil under cucumber plants was greater in comparison with the tomato samplings. Frankliniella occidentalis was found in greater numbers in comparison with T. tabaci. The date of sampling showed a significant interaction with soil depth, with the number of insects found increasing from the first to the last date of sampling.     

An immuno-marking technique for thrips

Rabbit immunoglobulin G (R‐IgG) was used successfully as an external mark for thrips. Females of both Thrips tabaci Lindeman and Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae) were marked with 1 mg ml^?1 R‐IgG solution with 1%‘Tween 20’ by the contact exposure method. Determining the retention of the mark was by running the rinsing solution of individual thrips in an enzyme‐linked immunosorbent assay (ELISA). The sandwich ELISA method was used with an additional biotin–avidin step. The threshold for a positive marking score was defined as three times the mean optical density readings of the negative control thrips. Under laboratory conditions, on bean pods, all marked thrips scored positive up to 6 days after marking (DAM). When marked thrips were kept in the laboratory on marigold flowers for 2 days, they all scored positive. When marked and unmarked thrips were placed together on these flowers, the mark was transferred to 10–20% of the unmarked thrips and they became positive. Under field conditions, on sticky traps covered with water‐base glue, 100, 80, and 20% of the marked T. tabaci scored positive by the 3rd, 6th, and 9th DAM, respectively. Under the same conditions 100, 90, and 10% of the marked F. occidentalis scored positive by the 3rd, 6th, and 9th DAM, respectively. The retention of the R‐IgG decreased significantly under conditions of wetness and high humidity. After 6 days on chive plants kept at 80–100% r.h., all marked thrips scored negative while on plants kept at 40–60% r.h., 85% of the marked thrips scored positive. Rabbit IgG can be used as an external marker for thrips. The suitability of this marking method for dispersal studies of these important pests needs to be evaluated.     

Studies on the transmission of velvet tobacco mottle virus by the mirid, Cyrtopeltis nicotianae

The minimum acquisition period of velvet tobacco mottle virus (VTMoV) by its mirid vector Cyrtopeltis nicotianae was about 1 min, with an increase in the rate of transmission (i.e. proportion of test plants infected) for acquisition periods up to 1000 min. Pre-acquisition starvation periods up to 18 h did not affect the rate of transmission. After an acquisition access period of 2 days, the minimum inoculation period was between 1 and 2 h and the rate of transmission increased with increasing inoculation time; when the acquisition access period was 1 h, or if vectors were fasted for 16 h after the 2 day acquisition, the rate of transmission was significantly lower. When mirids were transferred sequentially each day to a healthy plant after a 24 h acquisition feed, they transmitted intermittently for up to 10 days. Up to 50% of mirids transmitted after a moult and this was not due to the mirids probing the shed cuticles or exudates of infective insects. Mirids transmitted after a moult, following acquisition periods of 10, 100 or 1000 min. C. nicotianae transmitted solanum nodiflorum mottle virus (SNMV), sowbane mosaic virus (SoMV) and southern bean mosaic virus (SBMV), but not subterranean clover mottle virus (SCMoV), lucerne transient streak virus (LTSV), tobacco ringspot virus (TRSV), galinsoga mosaic virus (GMV), nor nicotiana velutina mosaic virus (NVMV). Tomato bushy stunt virus (TBSV) was transmitted to 1/58 test plants.