Density, dispersal, and feeding impact of western flower thrips (Thysanoptera: Thripidae) on flowering chrysanthemum at different spatial scales

Abstract.  1. This study evaluated the effect of dispersal on the density and feeding impact of a phytophagous insect in relation to the spatial distribution of its host plants.
2. The interaction between density, dispersal, and feeding impact of western flower thrips on flowering chrysanthemum was quantified at three spatial scales, with infested and uninfested plants either isolated in 0.25 m² individual cages, or enclosed together in 2.25 m² communal cages or 75 m² greenhouses.
3. In individual cages, the rate of dispersal from chrysanthemum plants to blue sticky traps increased with the density of thrips for females but not males. Uninfested plants consistently had fewer thrips when they were individually caged rather than enclosed with plants infested with adults, indicating that dispersal mediates inter-plant distribution of thrips.
4. The feeding impact of thrips on inflorescences was evaluated using the absorbance of ethanol extracts at wavelengths characteristic of yellow carotenoid pigments associated with chrysanthemum inflorescences (415, 445, and 472 nm). Increasing absorbance of extracts with increasing density of thrips per inflorescence suggests that feeding by thrips results in ruptured cells leaching carotenoid pigments.
5. In communal cages, the distribution of thrips was uniform for infested and uninfested plants, whereas the density and feeding impact of thrips in greenhouses were higher for infested than uninfested plants. These results suggest that short-range dispersal by adults homogenises the density and feeding impact of thrips among host plants only on a small spatial scale.     

Effects of tomato spotted wilt virus (TSWV) isolates, host plants, and temperature on survival, size, and development time of Frankliniella fusca

The effects of different isolates of the tomato spotted wilt tospovirus (TSWV), host plants, and temperatures on Frankliniella fusca (Hinds) (Thysanoptera: Thripidae), the most important vector of TSWV in North Carolina, were measured in the laboratory. Thrips were reared at either 18.3, 23.9, or 29.4 °C until adult eclosion on excised leaves of Datura stramonium L. or Emilia sonchifolia (L.). Plants were either infected with the TSWV isolates CFL or RG2, or left uninfected (control). The results revealed a positive relationship between larval survival and temperature, regardless of host plant or TSWV isolate. Both survival to adult and percentage transmission of TSWV by F. fusca were significantly affected by the interaction between host plant and TSWV isolate. The consequence of this interaction was that the cohort‐based percentage transmission from infected E. sonchifolia plants for CFL was 1.3‐fold greater than that of RG2, whereas the percentage transmission from infected D. stramonium plants for RG2 was twice that of CFL. Both host plant and TSWV isolates showed significant effects on thrips development time to adult and head capsule width of adult thrips, as well as on the incidence of thrips infection with TSWV. The infection status of these thrips was determined by ELISA for the NSs viral protein. Infected thrips reared on infected host foliage took longer to develop to adult and were smaller than non‐infected thrips which had also been reared on infected host foliage, demonstrating a direct effect of the TSWV on thrips. However, non‐infected thrips reared on non‐infected leaves took longer to develop than non‐infected thrips reared on infected leaves, suggesting an effect of the plant tissue on thrips. In addition, adult thrips reared on TSWV‐infected D. stramonium at 29.4 °C developed smaller head capsules than thrips developing on infected foliage at lower temperatures and on non‐infected leaves of D. stramonium or E. sonchifolia. Both TSWV isolates and host plants differentially affected females more than males. In conclusion, both the infection of thrips by TSWV and TSWV‐mediated changes in host plant quality were found to have significant biological effects on F. fusca.     

Leaf morphology of hosts and nonhosts of the thrips Heliothrips haemorrhoidalis (Bouché)

This study highlights the morphological differences between two groups of plants; those that are recorded as hosts of the thrips Heliothrips haemorrhoidalis (Bouché) and those that remain free from infestation. Scanning electron microscope techniques were used to describe the morphology of the leaf surface of 19 species in order to help identify which morphological features could play a role in the selection of plant species by thrips from among a diverse botanical collection. H. haemorrhoidalis had a preference for species with leaves that were coriaceous, with one or both surfaces being smooth. Plants evading these thrips commonly possessed glandular trichomes. Thus morphology may have a role in deterring thrips from the leaf surface, as well as influencing the behaviour of predators that control thrips. Further detailed studies into the chemistry of leaves of hosts and nonhost species may help to further our understanding of selection mechanisms.  © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 152 , 109–130.     

Molecular relationships between populations of South African citrus thrips (Scirtothrips aurantii Faure) in South Africa and Queensland, Australia

Abstract   In response to the recent establishment of a population of South African citrus thrips ( Scirtothrips aurantii Faure) in Australia, we used DNA sequence data to examine whether this population is distinct from populations in South Africa. Mitochondrial and internal transcribed spacer (ITS2) DNA from populations from different host plants in Australia and South Africa showed no clear separation between populations that was entirely congruent with host plant or country of origin. Analysis of the ITS2 data was confounded by the presence of multiple different copies of the spacer in some populations. Neither the presence or absence, nor the sequence of these copies was clearly diagnostic for any one population. These preliminary data suggest that the Australian population is not a distinct species or subspecies from the populations of S. aurantii on either citrus or Bryophyllum in South Africa.     

Predatory effect of Orius niger (Wolff) (Hem., Anthocoridae) on Frankliniella occidentalis (Pergande) and Thrips tabaci Lindeman (Thysan., Thripidae)

The predatory effect of adult female Orius niger (Wolff) (Hem., Anthocoridae) on the larvae I–II and adults of two injurious thrips , Frankliniella occidentalis (Pergande) and Thrips tabaci Lindeman (Thysan., Thripidae), was examined in June 1997, in controlled environment chambers (temperature 22 ± 0.2°C, 65 ± 3% RH, a 16 h light : 8 h dark photoperiod and light intensity 9000 Lux). This study took place on sweet pepper leaves ( Capsicum annuum L.) in transparent small plastic cages at proportions of 1/5, 1/10, 1/20 and 1/30 predator/number of thrips for larvae I–II and adults separately for each thrips species. O. niger was proved an effective predator for the immature stages (larvae I–II) and for the adults of the two thrips species. We concluded that O. niger could be used with success for the biological control of thrips in greenhouses crops.     

Populations of North American bean thrips, Caliothrips fasciatus (Pergande) (Thysanoptera: Thripidae: Panchaetothripinae) not detected in Australia

Abstract  Caliothrips fasciatus is native to the USA and western Mexico and overwintering adults are regular contaminants in the 'navel' of navel oranges exported from California, USA to Australia, New Zealand and elsewhere. Due to the long history of regular interceptions of C. fasciatus in Australia, a survey for this thrips was undertaken around airports, seaports, public recreational parks and major agricultural areas in the states of Queensland, New South Wales, Victoria, South Australia and Western Australia to determine whether C. fasciatus has successfully invaded Australia. Host plants that are known to support populations of C. fasciatus , such as various annual and perennial agricultural crops, urban ornamentals and weeds along with native Australian flora, were sampled for this thrips. A total of 4675 thrips specimens encompassing at least 76 species from a minimum of 47 genera, and three families were collected from at least 159 plant species in 67 families. Caliothrips striatopterus was collected in Queensland, but the target species, C. fasciatus , was not found anywhere. An undescribed genus of Thripidae, Panchaetothripinae, was collected from ornamental Grevillea (var. Robyn Gordon) at Perth (Western Australia) Domestic Airport, and is considered to be a native Australian species. This survey has provided valuable information on the background diversity of thrips species associated with various native and exotic plant species around major ports of entry and exit for four of five states in Australia. We suggest that the major reason C. fasciatus has not established in Australia is due to high adult mortality in navels that are kept at low storage temperatures (2.78°C) during an 18- to 24-day transit period from California to Australia.     

Biological studies of the Australian predatory mite Typhlodromips montdorensis (Schicha) (Acari: Phytoseiidae), a potential biocontrol agent for western flower thrips, Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae)

Abstract The biology of the Australian phytoseiid mite Typhlodromips montdorensis is described from material collected in Queensland and South Australia in 1994−1996. At 25°C, when fed on cumbungi ( Typha sp.) pollen, the life cycle was completed in approximately 7 days, with an intrinsic rate of natural increase ( r _m ) of 0.32. Female−male pairs produced a mean total of 52.7 eggs within 28 days of oviposition. Females that were deprived of males after first mating stopped laying eggs after 7−19 days; however, if another male was added, they resumed egg laying and produced, on average, a total of 49.4 eggs. The sex ratio was 2.24 females to one male. At 25°C, fecundity on a diet of thrips larvae (first-instar Frankliniella schultzei Trybom) was high, ranging from 2.72 to 3.58 eggs per day on the third day, depending on previous diet. Consumption rate of thrips was also high, with an average of 7.23−14.44 first-instar larvae eaten per day on the third day, depending again on previous diet and also on number of thrips larvae made available. The species was also observed to feed on: (i) broad mite, Polyphago­tarsonemus latus (Banks); (ii) tomato russet mite, Aculops lycopersici (Massee); and (iii) two-spotted mite, Tetranychus urticae Koch. No diapause was observed under conditions of 25°C, 8 h light and 10°C, 16 h dark. Eggs were sensitive to low humidity, with 50% failing to hatch below 70.8% relative humidity. This species is of interest as a candidate biological control agent for thrips, broad mite and tomato russet mite in protected crops.     

Spatiotemporal population dynamics of the banana rind thrips,Elixothrips brevisetis (Bagnall) (Thysanoptera: Thripidae)

The understanding of how environmental factors and agricultural practices affect population dynamics of insect pests is necessary for pest management. Here, we provide insight into the ecology of the banana rind thrips Elixothrips brevisetis (Bagnall) (Thysanoptera: Thripidae) by collecting and analysing a spatiotemporal database of population estimates in Martinique (West French Indies). We assessed the influence of climatic variables (which were rainfall and temperature) and biotic variables (which were banana and three weed species) on the adult thrips abundance for different components of the banana plant (sucker, mother plant and bunch) and evaluated the effect of thrips abundance and standard bunch covers on damages. The abundance of thrips on the sucker, the mother plant, and the bunch was significantly related to the abundance on neighbouring banana plants, and spatial autocorrelation indicated that E. brevisetis dispersed for only short distances. The number of thrips on the mother plant and on the bunch was positively related to the number of thrips on the sucker, suggesting that the thrips may disperse from the sucker to the mother plant and then to the bunch. The abundance of thrips on the sucker increased with sucker height and was positively correlated with the mean daily rainfall during the 17 days before sampling; the length of that period might correspond with the time required for an individual to complete its life cycle. Covered bunches had 98% fewer thrips than non‐covered bunches, and the damage caused by thrips was linearly related to the number of thrips present between the 2nd and 4th week after flowering. Finally, we found that the presence of Alocasia cucullata, Dieffenbachia seguine and Peperomia pellucida is significantly related with a decrease in thrips abundance on banana plants, suggesting the use of these weeds as potential trap plants.     

Winter and spring abundance of Frankliniella spp. and Thrips tabaci Lindeman (Thysan., Thripidae) on weed host plants in Turkey

Abstract:  The species composition of thrips and abundance of three pestiferous thrips species, Frankliniella occidentalis (Pergande), Thrips tabaci Lindeman and Frankliniella intonsa (Trybom) (Thysan., Thripidae) on weed species during winter and spring time were studied in vegetable production and polycultured areas in the eastern Mediterranean region of Turkey in years 2002 and 2003. Of a total of 61 543 thrips extracted from 8933 samples collected, 77% were adults. F. occidentalis was collected from all of 49 weed species sampled and F. intonsa was detected on 18 plant species between May and June. T. tabaci was collected from 42 of a total of 49 weed species. Immature thrips were extracted from 42 of a total of 49 weed species. Four weed species of a total 35 weed species sampled between April and May in the sampling areas hosted 63% of larvae and approximately 50% of F. occidentalis collected. A total of 23 thrips species was recorded from weeds sampled in this study. F. occidentalis accounted for 83% of a total 47 640 adult thrips collected and followed by low rates of T. tabaci and F. intonsa (9 and 1%, respectively). Melanthrips spp. accounted for 3.54% of total numbers of adult thrips. Flower-inhabiting thrips species and T. tabaci were most abundant on weeds between April and May when the number of weed species in bloom was greatest, then decreased to low levels after May. Most pestiferous thrips on weeds species were collected from vegetable production areas. F. occidentalis was the predominant thrips comprising over 80% in most months in the vegetable grown area. In polycultured area, the composition of adult thrips shifted monthly. While Melanthrips was the more prevailing thrips by rates 53% in February and 81% in March, F. occidentalis was the predominant thrips with 60 to 62% in spring, respectively.     

Mate Recognition in the South African Citrus Thrips Scirtothrips aurantii (Faure) and Cross-Mating Tests with Populations from Australia and South Africa

South African citrus thrips (Scirtothrips aurantii) is a pest of citrus, mango and other horticultural species in its native range, which encompasses a large part of Africa. Its adventitious establishment in Australia in 2002 was a major cause for concern. The thrips, 11 years after its incursion into Australia, has remained on plants of a single host plant genus Bryophyllum (Crassulaceae). Characterization of the Specific-Mate Recognition System of the Bryophyllum population of thrips present in Australia and behavioral bioassay experiments revealed that compounds found in the insects’ body extracts play a crucial role in mate recognition of S. aurantii. Reciprocal cross-mating experiments between the Australian Bryophyllum insects and South African S. aurantii from horticultural host plants showed that mating frequencies were significantly lower in test crosses (Bryophyllum x horticultural) than in controls (Bryophyllum x Bryophyllum or horticultural x horticultural), which indicates there are at least two distinct species within S. aurantii and suggests further tests of this interpretation. The results suggest that these tiny phytophagous insects localize mates through their association with a particular host plant species (or closely-related group of species). Also, specific tests are suggested for clarifying the species status of the host-associated populations of S. aurantii in Africa.     

The spread of the western flower thrips Frankliniella occidentalis (Pergande)

Abstract 1 Since the late 1970s, the western flower thrips has spread from its original distribution in western North America to become a major worldwide crop pest. 2 A wide range of data sources have been used to map the original distribution in the U.S.A. and Canada, and the progress of the spread in the U.S.A., Canada, Europe, northern Africa and Australia. 3 The possible reasons for the start of the spread are discussed. The most likely reason is that intensive insecticide use in horticulture in the 1970s and 1980s selected an insecticide resistant strain or strains. These then established in glasshouses across North America and spread from there to Europe, Asia, Africa and Australia. 4 The international spread of the western flower thrips occurred predominantly by the movement of horticultural material, such as cuttings, seedlings and potted plants. Within Europe, an outward spread from the original outbreak in the Netherlands is discernible. The speed of spread was 229 ± 20 km/year. 5 The spread has not been restricted to glasshouses. The western flower thrips has established outdoors in areas with milder winters; for example, across the southern U.S.A., southern Europe and Australia. It also overwinters in some regions with colder winters. 6 Polyphagous phytophagous thrips have many factors predisposing them to become worldwide crop pests, particularly in glasshouses. Some other species that might spread in a similar way to the western flower thrips are listed.     

Biological studies of the Australian predatory mite Typhlodromalus lailae (Schicha) (Acari: Phytoseiidae)

Abstract The biology of the Australian phytoseiid mite Typhlodromalus lailae is described from material collected in Western Australia and New South Wales in 1994. At 25°C, when fed on cumbungi ( Typha sp.) pollen, the life cycle is completed in approximately 6 days, with an intrinsic rate of natural increase ( r _m ), of 0.38. Female−male pairs produced a mean total of 44.6 eggs within 22 days of oviposition, with 39% of these females living in excess of 29 days. Females that were deprived of males after first mating stopped laying eggs after 4−9 days, but if another male was added they resumed egg laying and produced close to a full complement of eggs (mean 42 eggs). At 25°C, fecundity on a diet of cumbungi pollen or thrips larvae (first-instar Frankliniella schutzei Trybom) was high, averaging 3.71 and 3.33 eggs per day, respectively, over a 3-day period. The sex ratio was approximately 1.5 females to 1 male. Consumption rate of thrips was also high, with an average of approximately seven first-instar or two second-instar F. schultzei larvae eaten per day. The species was also observed to feed on broad mite, Polyphagotarsonemus latus (Banks), and tomato russet mite, Aculops lycopersici (Massee). No diapause was observed under conditions of 25°C 8 h light and 10°C 16 h dark. Eggs were sensitive to low humidity, with 50% failing to hatch below 71.1% relative humidity. This species is of interest as a candidate biological control agent for thrips, broad mite and tomato russet mite in protected crops.     

Australian Thysanoptera – biological diversity and a diversity of studies

Abstract   Studies in Australia on thrips have had extensive impacts worldwide. In behaviour, the latest definition of eusociality is derived from work on the radiation of thrips on Acacia species in central Australia, and these Acacia thrips also having been used to develop the concept of 'model clades' for analysing the evolution of behavioural and ecological diversity. In ecology, the concept of the lack of density dependent factors in population dynamics was elaborated through studies on the plague thrips of southern Australia. In virology, thrips were first shown in Australia to be the vectors of tospoviruses, although these viruses, their vectors and the plants attacked are all non-native to this continent. Work in Australia has included the development of electronic methods of illustration, identification and information transfer about thrips, including the use of molecular methods for pest species recognition, and considerable advances have been made in Australia in our knowledge of the relationships between thrips and plants, from polyphagy to pollination.     

Influences of fertilization on population abundance, distribution, and control of Frankliniella occidentalis on chrysanthemum

We examined the effects of fertilization on population abundance and within‐plant distribution of western flower thrips, Frankliniella occidentalis Pergande (Thysanoptera: Thripidae), on potted chrysanthemum, Dendranthema grandiflora (Tzvelev). We also investigated the effects of fertilization on the number of insecticide applications needed to control F. occidentalis on potted chrysanthemum. Under greenhouse conditions, rate of change in population abundance of F. occidentalis increased with fertilization levels from 0 to 100% of the standard fertilization level (375 ppm N) and was four times higher on plants fertilized with the standard level (rate of change = 0.14) than on plants fertilized with 0% during the first 4 weeks after thrips inoculation. Within‐plant distribution of F. occidentalis was influenced by the phenology of the plants rather than total nitrogen content of plant tissues. Prior to flower opening, more F. occidentalis were found in the middle region of the plants. When the flowers began to open, more thrips were found feeding inside the flowers than on the leaves. We further showed that production time, the time from transplantation to flower opening, shortened considerably with increased fertilization level. Production time was shortest, 12 weeks, for plants fertilized with 100% of the standard fertilization level. When the fertilization level was reduced to 20%, production time lengthened to 13 weeks. When fertilization level was reduced to 0%, production time lengthened to 14 weeks. Increased fertilization from 0 to 100% of the standard level did not result in higher numbers of insecticide applications. All three insecticides (acephate, bifenthrin, and spinosad) were effective in keeping the thrips infestation below a predetermined level, five thrips per plant, but bifenthrin required the most number of applications to do so. For chrysanthemum, a fast‐growing crop and heavy utilizer of fertilizer, fertilization influenced not only the population growth of pest insects but also plant production time. As a result, optimizing fertilization level to reduce pest population growth may be a useful tactic in an Integrated Pest Management program for managing F. occidentalis on potted chrysanthemum. However, the effect of fertilization on production time and plant quality should also be considered when implementing this tactic.     

Daily flight activity of the western flower thrips (Thysan., Thripidae) in nectarine orchards in British Columbia, Canada

Abstract:   Hourly flight patterns of western flower thrips, Frankliniella occidentalis (Pergande) (Thysan., Thripidae) were assessed over a 24 h period in two nectarine orchards located in the Similkameen Valley, British Columbia, on 13 separate occasions between March and October 1994. The numbers of western flower thrips (male or female, dark or pale morphs) trapped per hour at between four to eight heights (0.25–2.00 m) were compared with temperature, wind speed, time of year and location of trap placement. Traps were placed within orchards, at the border of orchards and adjacent wild land, and within wildlands. Temperature and wind speed thresholds are defined, although the effect of wind speed varied with height of flight. Height of flight was affected by both the height of prevalent vegetation and temperature, with mean height of flight increasing linearly with temperature. Numbers of thrips in flight decreased with height of sticky trap from the ground. The pale morph was generally more common than the dark morph of western flower thrips. Males were not present until after emergence of the first generation in May, and were found at an approximate ratio of 4 : 1 (F : M) for the rest of the year. There were no differences between sexes or morphs of western flower thrips for location, height or daily patterns of flight.     

Relationship between onion thrips (Thrips tabaci) and Stemphylium vesicarium in the development of Stemphylium leaf blight in onion

Stemphylium leaf blight caused by Stemphylium vesicarium and onion thrips (Thrips tabaci) are two common causes of leaf damage in onion production. Onion thrips is known to interact synergistically with pathogens to exacerbate plant disease. However, the potential relationship between onion thrips and Stemphylium leaf blight is unknown. In a series of controlled laboratory and field trials, the relationship between thrips feeding and movement on the development and severity of Stemphylium leaf blight were examined. In laboratory assays, onions (“Avalon” and “Ailsa Craig”) with varying levels of thrips feeding damage were inoculated with S. vesicarium. Pathogen colonisation and leaf dieback were measured after 2 weeks. In pathogen transfer assays, thrips were exposed to S. vesicarium conidia, transferred to onion and leaf disease development was monitored. In field trials, insecticide use was examined as a potential indirect means to reduce Stemphylium leaf blight disease and pathogen colonisation by reducing thrips damage. Results from laboratory trials revealed that a reduction in thrips feeding decreased S. vesicarium colonisation of onion leaves by 2.3–2.9 times, and decreased leaf dieback by 40–50%. Additionally, onion thrips were capable of transferring S. vesicarium conidia to onion plants (albeit at a low frequency of 2–14% of plants inoculated). In field trials, the symptoms and colonisation of Stemphylium leaf blight were reduced by 27 and 17%, respectively with the use of insecticide to control thrips. These results suggest that onion thrips may play a significant role in the development of Stemphylium leaf blight, and thrips control may reduce disease in commercial onion fields.     

Seasonal abundance and spatial distribution of larval and adult thrips (Thysanoptera) on weed host plants in mango orchards in Penang,Malaysia

The spatial distribution of larval and adult thrips (Thysanoptera) was studied on mango panicles, Mangifera indica L., on Penang Island, Malaysia, during two consecutive mango flowering seasons from December 2008 to March 2009 and from August to September 2009. Larval and adult thrips were sampled from mango panicles using the carbon dioxide (CO₂) collection technique weekly in treated and untreated orchards. Seasonal abundance and dispersion pattern of thrips were investigated on weed host plants in the treated orchard between June 2008 and March 2009. Spatiotemporal dynamics of larvae and adults was analyzed using Taylor’s Power Law (TPL), Lloyd’s Index (LI), and Green’s Index (GI). Thrips hawaiiensis (Morgan) was the dominant thrips species recovered from mango panicles and weeds in the treated orchard, whereas Scirtothrips dorsalis (Hood) was the most abundant species captured in the untreated orchard. Thrips adults and larvae analyzed via dispersion indices were found to be aggregated in mango panicles in both orchards. The value of the aggregation index (b) of TPL for the total number of adult thrips was significantly higher in the treated orchard than in the untreated orchard, whereas slopes of TPL for the total number of larval thrips did not differ significantly between treated and untreated orchards. All adult thrips species were distributed regularly on the weed plants; however, their larvae were aggregated. It is concluded that pesticide treatment caused adult thrips to become more aggregated on mango panicles, hiding in flower parts that were less exposed to the chemicals.     

Host-plant-mediated interaction between populations of a true omnivore and its herbivorous prey

Western flower thrips, Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae), are competitors with twospotted spider mites, Tetranychus urticae Koch (Acari: Tetranychidae), for plant resources and potential predators on spider mites when the opportunity arises. Which interaction predominates may depend on relative population densities and individual species’ responses to the plants on which they co‐occur. We examined interactions between populations of thrips and spider mites on several cultivars of two bedding plants: impatiens (Impatiens wallerana Hook.f) cultivars ‘Impulse Orange’ and ‘Cajun Carmine’, and ivy geranium [Pelargonium peltatum (L.) L’Her ex Aiton] cultivars ‘Sybil Holmes’ and ‘Amethyst 96’. Four combinations of thrips and mite numbers were studied: thrips alone, mites alone, and two densities of thrips and mites together. We compared population numbers after 4 weeks. Overall, mite numbers increased more rapidly than thrips did, but both species increased more rapidly on impatiens than on ivy geraniums. Between impatiens cultivars, thrips and mites increased more slowly on ‘Cajun Carmine’ (i.e., it was more resistant) than on ‘Impulse Orange’. On ivy geraniums, spider mites increased more slowly on ‘Sybil Holmes’ than on ‘Amethyst 96’ but the reverse was the case for thrips. Regardless of plant species or cultivar, thrips had a strong negative effect on spider mites whenever they co‐occurred, suppressing mite population growth by around 50% compared to when mites were alone. However, the effect of spider mites on western flower thrips depended on the quality of the plant species. On impatiens, thrips co‐occurring with spider mites increased slightly more than thrips alone did, while on ivy geranium mites had a small negative effect on thrips. Contrary to expectations, thrips had a larger negative impact on spider mites on plants that were more susceptible to thrips than they did on plants more resistant to thrips. We suggest that host plants mediate the interaction between an omnivore and its herbivorous prey not only by altering individual diet choice but by changing the relative population dynamics of each species.     

Sampling methods, dispersion patterns, and fixed precision sequential sampling plans for western flower thrips (Thysanoptera: Thripidae) and cotton fleahoppers (Hemiptera: Miridae) in cotton

A 2-yr field study was conducted to examine the effectiveness of two sampling methods (visual and plant washing techniques) for western flower thrips, Frankliniella occidentalis (Pergande), and five sampling methods (visual, beat bucket, drop cloth, sweep net, and vacuum) for cotton fleahopper, Pseudatomoscelis seriatus (Reuter), in Texas cotton, Gossypium hirsutum (L.), and to develop sequential sampling plans for each pest. The plant washing technique gave similar results to the visual method in detecting adult thrips, but the washing technique detected significantly higher number of thrips larvae compared with the visual sampling. Visual sampling detected the highest number of fleahoppers followed by beat bucket, drop cloth, vacuum, and sweep net sampling, with no significant difference in catch efficiency between vacuum and sweep net methods. However, based on fixed precision cost reliability, the sweep net sampling was the most cost-effective method followed by vacuum, beat bucket, drop cloth, and visual sampling. Taylor's Power Law analysis revealed that the field dispersion patterns of both thrips and fleahoppers were aggregated throughout the crop growing season. For thrips management decision based on visual sampling (0.25 precision), 15 plants were estimated to be the minimum sample size when the estimated population density was one thrips per plant, whereas the minimum sample size was nine plants when thrips density approached 10 thrips per plant. The minimum visual sample size for cotton fleahoppers was 16 plants when the density was one fleahopper per plant, but the sample size decreased rapidly with an increase in fleahopper density, requiring only four plants to be sampled when the density was 10 fleahoppers per plant. Sequential sampling plans were developed and validated with independent data for both thrips and cotton fleahoppers.     

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.