Phosphine Resistance in Cryptolestes ferrugineus (Coleoptera: Laemophloeidae) Collected From Grain Storage Facilities in Oklahoma, USA.

Phosphine gas (PH3) is one of the most commonly used fumigants for controlling stored-grain pests worldwide. We estimated the discriminating dose for Cryptolestes ferrugineus (Stephens) (Coleoptera: Laemophloeidae) adult insects using a laboratory susceptible strain. This discriminating dose was then used to determine presence or absence of PH3 resistance (resistance frequencies) in 19 field-collected populations of C. ferrugineus from Oklahoma, United States. The discriminating dose was estimated as 56.2 ppm of PH3 over a 20-h exposure period at 25 °C. Discriminating dose bioassay results showed that PH3 resistance was present in all 19 populations of C. ferrugineus tested. However, five populations-Stillwater (Stil), Enid Terminal 1 (ET-1), Enid Terminal 2 (ET-2), Johnson-Enid population (JE), and DK Farm 20 population (DK Farm 20) had ≥90% resistance frequencies. LC99 values estimated by probit analyses of dose-response mortality data for the laboratory susceptible strain (Lab-S), JE, and DK Farm 20 were 7.3, 636.4, and 968.6 ppm, respectively, over a 3-d exposure period. The level of resistance in DK Farm 20, the most resistant population, was 133.5 times that of the susceptible laboratory strain. This study shows that PH3 resistance in C. ferrugineus may be widespread in Oklahoma. Based on this study, there is a need for a wider PH3 resistance survey in grain-growing regions of Oklahoma and United States. Furthermore, results show there is a need to develop PH3 resistance management strategies for C. ferrugineus and other stored-product insect pest species to combat resistance and ensure continued effective future use of PH3.

Phosphine Resistance in Adult and Immature Life Stages of Tribolium castaneum (Coleoptera: Tenebrionidae) and Plodia interpunctella (Lepidoptera: Pyralidae) Populations in California.

Phosphine resistance in stored-product insects occurs worldwide and is a major challenge to continued effective use of this fumigant. We determined resistance frequencies and levels of resistance in Tribolium castaneum and Plodia interpunctella collected from California almond storage and processing facilities. Discriminating doses of phosphine were established for eggs and larvae of P. interpunctella and eggs of T. castaneum using laboratory susceptible strains of the two species. For T. castaneum and P. interpunctella eggs, discriminating doses were 62.4 and 107.8 ppm, respectively, over a 3-d fumigation period, and for P. interpunctella larvae, discriminating dose was 98.7 ppm over a 20-h fumigation period. Discriminating dose tests on adults and eggs showed that 4 out of 11 T. castaneum populations tested had resistance frequencies that ranged from 42 to 100% for adults and 54 to 100% for eggs. LC99 values for the susceptible and the most resistant adults of T. castaneum were 7.4 and 356.9 ppm over 3 d, respectively. LC99 values for T. castaneum eggs were 51.5 and 653.9 ppm, respectively. Based on adult data, the most resistant T. castaneum beetle population was 49× more resistant than the susceptible strain. Phosphine resistance frequencies in P. interpunctella eggs ranged from 4 to 20%. Results show phosphine resistance is present in both species in California. Future research will investigate phosphine resistance over a wider geographic area. In addition, the history of pest management practices in facilities where insects tested in this study originated will be determined in order to develop phosphine resistance management strategies for California almond storage and processing facilities.

Contact Toxicity of Deltamethrin Against Tribolium castaneum (Coleoptera: Tenebrionidae), Sitophilus oryzae (Coleoptera: Curculionidae), and Rhyzopertha dominica (Coleoptera: Bostrichidae) Adults.

This study was conducted at Oklahoma State University, Stillwater, OK, to evaluate the response to deltamethrin concentrations for adults of three stored-product insects, Tribolium castaneum (Herbst), Sitophilus oryzae (L.), and Rhyzopertha dominica (F.). In insect toxicological studies, knockdown is the state of intoxication and partial paralysis as a result of exposure to an insecticide. Deltamethrin concentrations ranging from 0.48 to 140 mg/m(2) (1 to 3,000 ppm) were sprayed on glass Petri dishes. After the dishes dried, 20 adult insects of each species were placed on the treated dishes to determine the contact toxicity of deltamethrin. Assessments for knockdown were made at 15-min intervals for up to 8 h after initial exposure and then again after 24 or 48 h. Insects were then transferred to clean untreated Petri dishes with diet and observed from 0.5 to 72 h. Mortality was assessed 72 h after transfer to untreated dishes with food material. Deltamethrin was highly effective against all three species tested and achieved 99% knockdown of insects of all species within 4 h after exposure at concentrations ≥1.2 mg/m(2) Although some insects recovered from initial knockdown at concentrations ≤48 mg/m(2), nearly all the insects were killed at 140 mg/m(2) when exposed for 48 h. LC95 values for all species tested, for the 48-h exposure period, were <140 mg/m(2), the concentration of deltamethrin that could potentially be present in new ZeroFly Storage Bag fabric. ZeroFly bags are used for stored-product insect pest control.

Population Growth and Development of the Psocid Liposcelis fusciceps (Psocoptera: Liposcelididae) at Constant Temperatures and Relative Humidities.

We investigated the effects of seven temperatures (22.5, 25.0, 27.5, 30.0, 32.5, 35.0, and 37.5°C) and four relative humidities (43, 55, 63, and 75%) on population growth and development of the psocid Liposcelis fusciceps Badonnel (Psocoptera: Liposcelididae). Results demonstrated that L. fusciceps did not survive at 43% RH, at all temperatures tested. At 55% RH, L. fusciceps did not survive at the highest three temperatures and no psocids survived at 37.5°C and 63% RH. The highest population growth was recorded at 30.0°C and 75% RH where populations increased 16-fold from an initial population of five females. L. fusciceps males have two to four nymphal instars, and the percentages of males with two, three, and four instars were 28, 70, and 2%, respectively. Female L. fusciceps have two to five instars, and the percentages of females with two, three, four, and five instars were 2, 33, 63, and 2%, respectively. The total developmental time for males was shorter than females. We developed temperature-dependent development equations for male and female eggs, individual nymphal, combined nymphal, and combined immature stages. Based on 30-d population growth, L. fusciceps can survive and multiply at a relative humidity of 55% at 22.5-30.0°C, but does better at 27.5-32.5°C and a higher relative humidity of 75%. Relative humidities of ≤ 63% and temperatures of ≥ 32.5°C are detrimental to L. fusciceps. These data provide a better understanding of L. fusciceps population dynamics and can be used to develop effective management strategies for this psocid.

Microsatellite markers for Cryptolestes ferrugineus (Coleoptera: Laemophloeidae) and other Cryptolestes species.

Cryptolestes ferrugineus (Stephens, 1831) is an important insect pest of stored products. Due to its broad host range, short life cycle, and high reproductive capacity, this species has rapidly colonized temperate and tropical regions around the world. In this study, we isolated 18 novel polymorphic microsatellite loci from an enriched genomic library based on a biotin/streptavidin capture protocol. These loci will be useful tool to better understand the genetic structure and migration patterns of C. ferrugineus throughout the world. The genetic parameters were estimated based on 80 individual C. ferrugineus from two natural populations. The results revealed that 18 loci were different polymorphic levels. The numbers of alleles ranged from 3 to 12, and eleven loci demonstrated polymorphic information contents greater than 0.5. The observed (H O) and expected (H E) heterozygosities ranged from 0.051 to 0.883 and 0.173 to 0.815, respectively. Five locus/population combinations significantly deviated from Hardy-Weinberg equilibrium. We also demonstrated the potential utility of the C. ferrugineus microsatellites as population and species markers for four additional Cryptolestes species.

COI barcode based species-specific primers for identification of five species of stored-product pests from genus Cryptolestes (Coleoptera: Laemophloeidae).

Flat grain beetles of the genus Cryptolestes (Coleoptera: Laemophloeidae) are one of the economically most important stored-product pests which feed on many kinds of agricultural products, especially grains. Nine of more than 40 described Cryptolestes species are recognized as stored-product pests and two of the pest species have a cosmopolitan distribution. Given the rapid growth in global trade of food products, ecological barriers to the spread of pests are easily overcome. Therefore, development of reliable systems for routine quarantine inspection and early infestation detection is vital. In the present study, we established a new rapid and accurate cytochrome c oxidase subunit I-based system for molecular identification of five common stored-product Cryptolestes species, namely, Cryptolestes capensis, Cryptolestes ferrugineus, Cryptolestes pusilloides, Cryptolestes pusillus and Cryptolestes turcicus. Five species-specific primer pairs for traditional uniplex polymerase chain reaction assay are described and their specificity and sensitivity for the identification process is evaluated using larval samples of 12 different populations from three continents (Asia, Europe and North America).

DNA barcoding of five common stored-product pest species of genus Cryptolestes (Coleoptera: Laemophloeidae).

Several species of the genus Cryptolestes Ganglbauer, 1899 (Coleoptera: Laemophloeidae) are commonly found in stored products. In this study, five species of Cryptolestes, with almost worldwide distribution, were obtained from laboratories in China, Czech Republic and the USA: Cryptolestes ferrugineus (Stephens, 1831), Cryptolestes pusillus (Schönherr, 1817), Cryptolestes turcicus (Grouvelle, 1876), Cryptolestes pusilloides (Steel & Howe, 1952) and Cryptolestes capensis (Waltl, 1834). Molecular identification based on a 658 bp fragment from the mitochondrial DNA cytochrome c oxidase subunit I (COI) was adopted to overcome some problems of morphological identification of Cryptolestes species. The utility of COI sequences as DNA barcodes in discriminating the five Cryptolestes species was evaluated on adults and larvae by analysing Kimura 2-parameter distances, phylogenetic tree and haplotype networks. The results showed that molecular approaches based on DNA barcodes were able to accurately identify these species. This is the first study using DNA barcoding to identify Cryptolestes species and the gathered DNA sequences will complement the biological barcode database.

Weight loss and germination failure caused by psocids in different wheat varieties.

We investigated weight loss caused by Liposcelis entomophila (Enderlein) feeding in damaged (cracked) and intact kernels of 'Jagger' variety of hard red winter wheat over a 90-d period at 30 +/- 1 degrees C and 75 +/- 5% relative humidity. L. entomophila caused 8.5% weight loss in damaged wheat kernels, which was significantly greater than the weight loss found in intact wheat kernels (0.2%). We also evaluated the suitability of six wheat varieties commonly grown in Oklahoma, namely, Jagger, 'Endurance,' 'Overley,' 'Jagalene,' 'OK Bullet,' and 'Deliver' to support populations of four psocid species, namely, Liposcelis bostrychophila Badonnel, L. decolor (Pearman), L. entomophila, and L. paeta Pearman over a 30-d period. The greatest population increase was observed in L. bostrychophila followed by L. paeta. Subsequently, weight loss of damaged and intact wheat kernels and germination of intact kernels infested by L. paeta over a 45-d period were assessed in OK Bullet variety. L. paeta caused weight loss of 3.3% in damaged kernels, which was significantly greater than the weight loss found in intact kernels (0.4%). Based on our data, 40% of infested intact kernels failed to germinate after 45 d of infestation by L. paeta, but this decreased to 32% when adjusted using germination failure of uninfested kernels. Our data show that psocid infestations do not only cause considerable loss in weight of wheat, but also result in significant germination failure. These data call for the formulation of effective integrated psocid management strategies for stored wheat to mitigate the negative impacts of psocid pests.

Phosphine resistance in Tribolium castaneum and Rhyzopertha dominica from stored wheat in Oklahoma.

Phosphine gas, or hydrogen phosphide (PH3), is the most common insecticide applied to durable stored products worldwide and is routinely used in the United States for treatment of bulk-stored cereal grains and other durable stored products. Research from the late 1980s revealed low frequencies of resistance to various residual grain protectant insecticides and to phosphine in grain insect species collected in Oklahoma. The present work, which used the same previously established discriminating dose bioassays for phosphine toxicity as in the earlier study, evaluated adults of nine different populations of red flour beetle, Tribolium castaneum (Herbst), and five populations of lesser grain borer, Rhyzopertha dominica (F.) collected from different geographic locations in Oklahoma. One additional population for each species was a laboratory susceptible strain. Discriminating dose assays determined eight out of the nine T. castaneum populations, and all five populations of R. dominica, contained phosphine-resistant individuals, and highest resistance frequencies were 94 and 98%, respectively. Dose-response bioassays and logit analyses determined that LC99 values were approximately 3 ppm for susceptible and 377 ppm for resistant T. castaneum, and approximately 2 ppm for susceptible and 3,430 ppm for resistant R. dominica. The most resistant T. castaneum population was 119-fold more resistant than the susceptible strain and the most resistant R. dominica population was over 1,500-fold more resistant. Results suggest a substantial increase in phosphine resistance in these major stored-wheat pests in the past 21 yr, and these levels of resistance to phosphine approach those reported for other stored-grain pest species in other countries.

Efficacy of heat treatment for disinfestation of concrete grain silos.

Field experiments were conducted in 2007 and 2008 to evaluate heat treatment for disinfestations of empty concrete elevator silos. A Mobile Heat Treatment Unit was used to introduce heat into silos to attain target conditions of 50 degrees C for at least 6 h. Ventilated plastic containers with a capacity of 100 g of wheat, Triticum aestivum L., held Rhyzopertha dominica (F.) (Coleoptera: Bostrichidae) and Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae). Polyvinyl chloride containers with a capacity of 300 g of wheat held adults of Liposcelis corrodens (Heymons) (Psocoptera: Liposcelididae) and Liposcelis decolor (Pearman), which were contained in 35-mm Petri dishes within the grain. Containers were fastened to a rope suspended from the top of the silo at depths of 0 m (just under the top manhole), 10 m, 20 m, and 30 m (silo floor). When the highest temperature achieved was approximately 50 degrees C for 6 h, parental mortality ofR. dominica and T. castaneum, and both psocid species was 98-100%. Progeny production of R. dominica occurred when there was parental survival, but in general R. dominica seemed less impacted by the heat treatment than T. castaneum. There was 100% mortality of L. corrodens at all depths in the heat treatments but only 92.5% mortality for L. decolor, with most survivors located in the bioassay containers at the top of the silo. Results show wheat kernels may have an insulating effect and heat treatment might be more effective when used in conjunction with sanitation and cleaning procedures.

Efficacy of ozone fumigation against the major grain pests in stored wheat.

Field experiments were conducted in steel bins containing 13,600 kg of hard red winter wheat, Triiticum aestivum L. One bin was treated with ozone and the second bin served as a control. Stored grain insects were placed in bins for 1-, 2-, 3-, and 4-d exposure periods in sampling tubes to test ozone concentrations of 0, 25, 50, and 70 parts per million by volume (ppmv). Ozone treatments on eggs and larvae of Plodia interpunctella (Hübner) were not effective, but pupae were more susceptible. Sitophilus oryzae (L.) adults were the most susceptible species with 100% mortality reached after 2 d in all ozone treatments. However, some progeny were produced at all concentrations and exposure periods. Tribolium castaneum (Herbst) adults had 100% mortality only after 4 d at 50 or 70 ppmv. No T. castaneum progeny were produced after 2-4 d at 70 ppmv. For Rhyzopertha dominica (F.), Cryptolestes ferrugineus (Stephens), and Oryzaephilus surinamensis (L.), 100% mortality was never achieved and progeny were produced at all ozone concentrations. Laboratory experiments, testing the effectiveness of ozone in controlling psocids, were conducted in two polyvinyl chloride cylinders each containing 55 kg of hard red winter wheat. Ozone treatment at a concentration of 70 ppmv was highly effective against adult female Liposcelis bostrychophila Badonnel and Liposcelis paeta Pearman after only 1 d of exposure. However, it was not effective against eggs of both species at all exposure periods. Ozonation has potential for the control of some stored grain insect pests on wheat.

Population growth and development of Liposcelis pearmani (Psocoptera: Liposcelididae) at constant temperatures and relative humidities.

Psocids of genus Liposcelis are now considered serious pests of stored products. We investigated the effects of eight temperatures (22.5, 25.0, 27.5, 30.0, 32.5, 35.0, 37.5, and 40.0°C) and four relative humidities (43, 55, 63, and 75%) on population growth and development of the psocid Liposcelis pearmani Lienhard. L. pearmani did not survive at 37.5 and 40.0°C, at all relative humidities tested; at 43% RH, at all temperatures tested; and at 55% RH, at 32.5 and 35°C. The greatest population growth was recorded at 32.5°C and 75% RH (32-fold growth). L. pearmani males have two to four nymphal instars, and the percentages of males with two, three, and four instars were 17, 63, and 20%, respectively. Female L. pearmani have two to five instars, and the percentages of females with two, three, four, and five instars were 5, 39, 55, and 1%, respectively. We developed temperature-dependent development equations for male and female eggs, individual nymphal, combined nymphal, and combined immature stages. Based on 30-d population growth, L. pearmani cannot survive at temperatures >35.0°C; does not thrive at low relative humidities (55%), at temperatures above 25°C; and has a high optimum relative humidity for population growth (75%). Therefore, we expect it to have a more limited distribution compared with other Liposcelis species. These data provide a better understanding of how temperature and RH may influence L. pearmani population dynamics and can be used in population growth models to help develop effective management strategies for this psocid, and to predict its occurrence.

Population growth and development of the psocid Liposcelis rufa (Psocoptera: Liposcelididae) at constant temperatures and relative humidities.

We investigated the effects of eight temperatures (22.5, 25.0, 27.5, 30.0, 32.5, 35.0, 37.5, and 40.0 degrees C) and four relative humidities (43, 55, 63, and 75%) on population growth and development of the psocid Liposcelis rufa Broadhead (Psocoptera: Liposcelididae). L. rufa did not survive at 43% RH, at all temperatures tested; at 55% RH, at the highest four temperatures; and at 63% RH and 40.0 degrees C. The greatest population growth was recorded at 35.0 degrees C and 75% RH (73-fold growth). At 40.0 degrees C, L. rufa populations declined or barely grew. L. rufa males have two to four nymphal instars, and the percentages of males with two, three, and four instars were 31, 54, and 15%, respectively. Female L. rufa have two to five instars, and the percentages of females with two, three, four, and five instars were 2, 44, 42, and 12%, respectively. The life cycle was shorter for males than females. We developed temperature-dependent developmental equations for male and female eggs, individual nymphal, combined nymphal, and combined immature stages. The ability of L. rufa to reproduce at a relative humidity of 55% and temperatures of 22.5-30.0 degrees C and at relative humidities of 63-75% and temperatures of 22.5-37.5 degrees C, in addition to being able to survive at 40.0 degrees C, suggests that this species would be expected to have a broader distribution than other Liposcelis species. These data provide a better understanding of L. rufa population dynamics and can be used to help develop effective management strategies for this psocid.

Reproductive parameters of the parthenogenetic psocid Lepinotus reticulatus (Psocoptera: Trogiidae) at constant temperatures.

We investigated effects of temperature, at 70% RH, on the reproductive parameters of the parthenogenetic psocid Lepinotus reticulatus Enderlein (Psocoptera: Trogiidae). The lowest fecundity (21) was at 35 degrees C and the highest (41) at 27.5 degrees C. At 22.5, 25, and 27.5 degrees C, peak oviposition rates (eggs/female/week) occurred in week 3 and were 4.7, 6.6, and 7.8, respectively; also 51, 57, and 62%, respectively, of all eggs were laid in the first 4 wk. At 30, 32.5, and 35 degrees C, peak oviposition rates occurred in week 2 and were 8.2, 9.0, and 7.4, respectively; 80, 85, and 98%, respectively, of all eggs were laid in the first 4 wk. The longest preoviposition period (4.4 d) was at 22.5 and 25 degrees C, and the longest postoviposition period (13.1 d) was at 22.5 degrees C. Oviposition period and longevity decreased with increasing temperature; at 22.5 degrees C, these parameters were 66 and 83 d, respectively, and at 35 degrees C, they were 18 and 24 d, respectively. Mean weekly oviposition rate increased with temperature and was highest at 32.5 degrees C (5.8 eggs/female/week). At 22.5, 25, 27.5, 30, 32.5, and 35 degrees C, it took 29, 20, 12, 11, 8, and 6 wk, respectively, for all females to die. Intrinsic rate of population increase increased with temperature until 32.5 degrees C (0.128) and then declined. We have developed temperature-dependent equations for preoviposition period, postoviposition period, oviposition period, oviposition rate, and longevity. Reproductive parameters affect population dynamics, and information on these parameters can be used in simulation models to predict L. reticulatus population dynamics to aid in developing effective management strategies.

Predicting stored grain insect population densities using an electronic probe trap.

Manual sampling of insects in stored grain is a laborious and time-consuming process. Automation of grain sampling should help to increase the adoption of stored grain integrated pest management. A new commercial electronic grain probe trap (OPI Insector) has recently been marketed. We field tested OPI Insector electronic grain probes in two bins, each containing 32.6 tonnes of wheat, Triticum aestivum L., over a 2-yr period. We developed new statistical models to convert Insector catch into insects per kilogram. We compared grain sample estimates of insect density (insects per kilogram of wheat) taken near each Insector to the model-predicted insect density by using Insector counts. An existing expert system, Stored Grain Advisor Pro, was modified to automatically read the Insector database and use the appropriate model to estimate Cryptolestes ferrugineus (Stephens), Rhyzopertha dominica (F.), and Tribolium castaneum (Herbst) density from trap catch counts. Management decisions using Insector trap-catch estimates for insect density were similar to those made using grain sample estimates of insect density for most sampling dates. However, because of the similarity in size of R. dominica and T. castaneum, the software was unable to differentiate counts between these two species. In the central and southern portions of the United States, where both species frequently occur, it may be necessary to determine the proportion of each species present in the grain by manual inspection of trap catch. The combination of SGA Pro with the OPI Insector system should prove to be a useful tool for automatic monitoring of insect pests in stored grain.

Sampling plans for the psocids Liposcelis entomophila and Liposcelis decolor (Psocoptera: Liposcelididae) in steel bins containing wheat.

Psocids are an emerging problem in grain storage, handling, and processing facilities in the United States. We used data from two steel bins each containing 32.6 metric tonnes of wheat, Triticum aestivum L., to develop sampling plans for Liposcelis entomophila (Enderlein), Liposcelis decolor (Pearman) (both Psocoptera: Liposcelididae), and a mixture of the two species. Taylor's coefficients a (a sampling factor) and b (an index of aggregation) for these pests were calculated and incorporated into sampling protocols to improve accuracy. The optimal binomial sample sizes for estimating populations of these psocids at densities of < 25 psocids per refuge were large; therefore, we recommend the use of numerical sampling within this range of densities. Numerical sampling of L. entomophila and L. decolor at densities of < 25 psocids per refuge should not be too laborious given the low psocid numbers involved; we recommend using 10 refuges per bin. For presence-absence sampling of L. entomophila or L. decolor, 20 refuges per bin should be used at densities of 25-100 psocids per refuge. The sampling plans we have developed based on the use of cardboard refuges are convenient for use in steel bins containing wheat because they are inexpensive, provide a rapid assessment of psocid population incidence, and are easy to implement. These sampling plans can be used to monitor populations of and the efficacy of management strategies used against L. entomophila and L. decolor.

Population growth and development of the psocid Liposcelis brunnea (Psocoptera: Liposcelididae) at constant temperatures and relative humidities.

We studied the effects of temperature and relative humidity on population growth and development of the psocid Liposcelis brunnea Motschulsky. L. brunnea did not survive at 43% RH, but populations increased from 22.5 to 32.5 degrees C and 55-75% RH. Interestingly, we found population growth was higher at 63% RH than at 75% RH, and the greatest population growth was recorded at 32.5 degrees C and 63% RH. At 35 degrees C, L. brunnea nymphal survivorship was 33%, and populations declined or barely grew. L. brunnea males have two to four nymphal instars, and the percentages of males with two, three, and four instars were 13, 82, and 5%, respectively. Female L. brunnea have three to five instars, and the percentages of females with three, four, and five instars were 18, 78, and 4%, respectively. The life cycle was shorter for males than females. We developed temperature-dependent development equations for male and female eggs, individual nymphal, combined nymphal, and combined immature stages and nymphal survivorship. The ability of L. brunnea to multiply rather rapidly at 55% RH may allow it to thrive under conditions of low relative humidity where other Liposcelis species may not. These data give us a better understanding of L. brunnea population dynamics and can be used to help develop effective management strategies for this psocid.

Temporospatial distribution of the psocids Liposcelis entomophila and L. decolor (Psocoptera: Liposcelididae) in steel bins containing wheat.

We studied the temporospatial distribution of psocids in steel bins containing 32.6 tonnes of wheat in 2005 and 2006 in Manhattan, KS. Psocids were sampled in the top 0.9 m of wheat using a 1.2-m open-ended trier; samples were taken from the bin center and in the four cardinal directions at 0.15 and 0.76 m from the bin wall. In addition, a 2.4-m partitioned grain trier with 16 compartments was used to sample psocids from a 2-m-diameter circle in the center of the bins and to a depth of 1.96 m. Only two species of psocids were identified in the study: Liposcelis entomophila in 2005 and L. decolor in 2006. Densities of psocids were low immediately after bins were filled in July 2005, peaked in October, dropped to almost zero in December as temperatures decreased, and remained at low levels until the study was ended in March. In 2006, densities of psocids increased gradually from August to mid-October and declined until the study was ended in early November. During the fall, psocids were more abundant at the center of the bin and at lower depths. In October to November of both years, the temperatures and moisture contents of grain in the center also were higher than that in other locations. This is the first report of temporospatial distribution of psocids in steel bins of wheat.

Evaluation of five sampling methods for the psocids Liposcelis entomophila and L. decolor (Psocoptera: Liposcelididae) in steel bins containing wheat.

An evaluation of five sampling methods for studying psocid population levels was conducted in two steel bins containing 32.6 tonnes of wheat in Manhattan, KS. Psocids were sampled using a 1.2-m open-ended trier, corrugated cardboard refuges placed on the underside of the bin hatch or the surface of the grain, and manual or automated electronic counts from Insector probe traps. Only two species were identified in this study: Liposcelis entomophila (Enderlein) in 2005 and L. decolor (Pearman) in 2006. In both years, psocid numbers started to increase in early September, peaked earliest in surface refuges, and peaked at nearly the same time in grain samples and manual and electronic Insector counts. No psocids were found in hatch refuges in December to February, although psocids were detected by the other sampling methods during this time. Numbers of psocids in the grain samples could be estimated from the numbers of psocids obtained using the cardboard refuges and Insector probe traps in both years. The results indicate that cardboard refuges or Insectors may provide an effective method for sampling psocids in bins of wheat.

Population growth and development of psocid Lepinotus reticulatus at constant temperatures and relative humidities.

We investigated the effects of temperature and relative humidity on population growth and development of the psocid Lepinotus reticulatus Enderlein. Part of this study assessed the effects of marking psocids by using methylene blue, chalk powder, and fluorescent powder to differentiate nymphal stages during development. We found that marking psocids by using methylene blue increased mortality and took twice as long to accomplish compared with marking by using fluorescent powder. Using chalk powder shortened the duration of third and fourth nymphal instars. Marking psocids by using fluorescent powder had no effect on mortality or duration of nymphal instars. Therefore, we recommend using fluorescent powder for marking psocids. L. reticulatus did not survive at 32, 43, and 55% RH, whereas populations increased from 22.5 to 32.5 degrees C at 75% RH. The largest population growth was recorded at 30 and 32.5 degrees C, whereas only 9% of nymphs developed to adults and populations declined at 35 degrees C. We developed temperature-dependent developmental equations for eggs, individual nymphal, combined nymphal, and combined immature stages. These equations showed predicted optimal temperatures for the development of eggs, combined nymphal, and combined immature stages to be 32.3, 34.5, and 34.4 degrees C, respectively; development at these temperatures was completed in 6.3, 16.7, and 23.3 d, respectively. Our study shows that psocids that consume their exuviae develop faster than those that do not, and this effect is more pronounced at lower temperatures. These data give us better understanding of L. reticulatus population dynamics, and they can be used to develop effective management strategies for this psocid.