SLIDE 1 Overview of the USDA-ARS Center for Grain and Animal Health Research and Stored Product Insect Research Unit in Manhattan, Kansas
U.S. Department of Agriculture, Agricultural Research Service, Center for Grain and Animal Health Research , 1515 College Avenue, Manhattan, KS, USA
James E. Throne
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Center for Grain and Animal Health Research Agricultural Research Service
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CGAHR has five research units - four located in main facility on 12 acre (4 hectare) site and one unit on Kansas State University campus
50,000 bu (700 mt) Research Grain Elevator Main facility
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Engineering and Wind Erosion Research Unit
4 scientists Develop technologies for rapid, automated
assessment of grain quality – detecting disease, mycotoxins, or insect infestation; quantifying protein and other quality traits
Develop techniques for safe storage of grain –
identity preservation, dust reduction
Control wind erosion of the soil – Wind Erosion
Prediction System
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Grain Quality & Structure Research Unit 5 scientists Determine grain characteristics and components responsible for end-use quality – e.g., which proteins in wheat affect bread rising Find new uses for sorghum
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Hessian fly Leaf Rust Karnal bunt Head Scab
Hard Winter Wheat Genetics Research Unit
6 scientists Develop disease- and
insect-resistant wheat that can tolerate environmental stresses
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Arthropod-Borne Animal Diseases Research Unit
7 scientists Conduct research to solve major endemic, emerging, and
exotic arthropod-borne disease problems in U.S. livestock
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Stored Product Insect Research Unit
7 scientists Develop environmentally friendly and cost-effective methods
to control stored-product insect pests
SLIDE 9 Which stored products do we work with?
- Bulk grains in bins and elevators
- Milling, processing, and warehouse industry
- Transportation industry - railcars, ships
- Urban environments - stores, homes
SLIDE 10 Why work on stored-product insects?
- Insects reduce the quality of stored grain and other stored products
in the U.S. and throughout the world.
- Over 10 billion bushels (254 million metric tons) of corn, 2 billion
bushels (54 million metric tons) of wheat, and about a billion bushels (27 million metric tons) of barley, oats, rice, rye, and sorghum are grown in the U.S. each year, with a value of over 44 billion dollars.
- It is estimated that postharvest losses to these grains due to insects
are 5 to 10% in the U.S., or about 2.2 to 4.4 billion dollars per year.
- Losses in developing countries are estimated at 30 to 50%.
- Losses to processed commodities are difficult to quantify, but
probably greatly exceed the losses to raw commodities.
- Many of the insecticides used by the cereal foods industry are being
lost due to insecticide resistance or regulatory changes, so we need alternative control technologies.
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- Dr. Frank Arthur
- Integrated Pest
Management
He conducts studies to determine
- ptimal use of insecticides,
particularly reduced-risk insecticides and aerosols, to help industry optimize insecticide use in stored grain and in processing
- facilities. He investigates effects of
various factors such as temperature, relative humidity, and sanitation on efficacy of insecticides.
SLIDE 12
- Dr. Jeff Lord
- Insect pathology
Many of the reduced-risk control technologies have lower efficacy than conventional insecticides, so we are looking for ways to synergize insect pathogens to make them more effective, such as combining the fungus Beauveria bassiana with diatomaceous earth.
Check Bb DE Bb+DE 43 75 50 100 150 200 250 300 350 400
30oC
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- Dr. Paul Flinn
- Expert Systems
The expert system Stored Grain Advisor was developed to aid in pest management in farm-stored wheat. Stored Grain Advisor Pro was developed to predict risk of insect problems in grain stored at elevators.
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- Dr. Paul Flinn
- Biological control
These small parasitic wasps attack beetle larvae in stored
reducing the grain temperature using aeration in the summer, these beneficial insects were 10 times more effective.
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- Dr. Paul Flinn
- Biological control
Matt Grieshop was a graduate student studying the behavior and ecology of tiny parasitoid wasps that are used to suppress moth pests in retail environments.
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- Dr. Jim Throne
- Ecology and sampling
We conducted a study that showed that the current grain buying practice based on insect-damaged kernels (IDK) is not a reliable indicator of insect infestation in railcars of wheat because there is not a clear relationship between IDK and the insect infestation level present in the grain.
SLIDE 18 Entomological applications of near-infrared spectroscopy developed include detection of insect-infested kernels and quantification of insect fragments in flour.
- Dr. Jim Throne
- Ecology and sampling
SLIDE 19 Insects developing inside kernels can be detected using digital X-ray technology.
- Dr. Jim Throne
- Ecology and sampling
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X-rays provide the most accurate estimate of internal
insect infestation, but the method is laborious and expensive Digital x-ray images obtained with Faxitron MX-20 Lesser grain borers in rice
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Digital x-ray images obtained with Faxitron MX-20 Rice weevils in rice
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Digital x-ray images obtained with Faxitron MX-20 Lesser grain borers in wheat
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Digital x-rays are very rapid, but equipment is expensive and can scan only a 10 X 10 cm (4 X 4 inch) area at a time – ca. 5 grams of wheat or ca. 175 kernels
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Electrically Conductive Mill
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Electrically Conductive Mill - Commercial version processes 2 kg/min
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Electrically Conductive Mill
Insect stage Detection rate 2nd or 3rd instar 74% 4th instar or pupae 83%
No false positives
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- High detection rate for large larvae and pupae
and 0% false positive rate
- Only works for live insects because it measures
moisture; this could be a problem for grain that has been fumigated and destined for milling
- Able to inspect 2 kg in a minute with no sample
preparation
Electrically Conductive Mill
SLIDE 35 Current studies are on ecology and control of psocids, an emerging pest of stored grain and processing, warehouse, and retail facilities, such as determining efficacy of heat, aerosols, and crack and crevice treatments for control
temperature and grain type for development.
% of original number of nymphs surviving to adults
Aerosol treatments
Control Methoprene Carrier EsfenvalerateCombined
% surviving to adults
20 40 60 80 100
Liposcelis entomophila
SLIDE 36 Most psocid pests of stored products are from the genus Liposcelis
- 7 species of Liposcelis and Lepinotus that are pests
- f stored products have been reported from the
U.S.; they don’t have common names and they are difficult to identify to species
- Lepinotus reticulatus, Liposcelis bostrychophila,
Liposcelis brunnea, Liposcelis corrodens, Liposcelis decolor, Liposcelis entomophila, and Liposcelis paeta
- The first two species are parthenogenetic
SLIDE 37 Grain samples
1 10 100 Bin 1 - 248 total psocids Bin 2 - 299 total psocids
Surface Refuges
1 10 100 1000 10000 Bin 1 - 14,829 total psocids Bin 2 - 18,786 total psocids
Hatch Refuges log(Number of psocids + 1)
1 10 100 1000 Bin 1 - 1,427 total psocids Bin 2 - 1,968 total psocids
Manual Insector Counts
10 100 1000 10000 Bin 1 - 45,284 total psocids Bin 2 - 32,218 total psocids
Electronic Insector Counts
Sep Oct Nov Dec Jan Feb Mar
10 100 1000 10000 Bin 1 - 29,902 total psocids Bin 2 - 35,153 total psocids
2005 Psocid trends – 115,059 psocids collected
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95% FL (hours) at: Temperature (oC) Lepinotus reticulatus Liposcelis entomophila LT95 37.5 90.92 (93.00-102.35) 111.43 (100.19-126.88) 40.0 13.83 (12.59-15.56) 43.52 (39.90-48.23) 42.5 3.84 (3.50-4.36) 9.06 (6.96-15.68) 45.0 0.70 (0.67-0.74) 5.51 (5.16-5.95) 47.5 0.66 (0.63-0.70) 1.89 (1.81-1.99)
We determined how long it takes to kill adult psocids at different temperatures Psocids appear to be very susceptible to heat, particularly Lepinotus reticulatus, but they are known to leave a facility to escape fumigants
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Chlorfenapyr and β-cyfluthrin provided efficient control of Liposcelis bostrychophila and L. entomophila at the label rates, unlike pyrethrin
Insecticide Liposcelis species LT95 (95% FL) [hours] β-Cyfluthrin entomophila 12.5 (11.7-13.6) bostrychophila 15.3 (14.6-16.2) Chlorfenapyr entomophila 5.1 (4.9-5.4) bostrychophila 7.7 (6.9-9.1) Pyrethrin entomophila 102.1 (94.6-112.5) bostrychophila 195.8 (158.3-280.1)
Chlorfenapyr is derived from a class of microbially-produced compounds
known as halogenated pyrroles; β-Cyfluthrin is a synthetic pyrethroid
SLIDE 40 20 40 60 80 100 1 1.5 2 4 6 8 10 12 24 48 96
20 40 60 80 100 1 1.5 2 4 6 8 10 12 24 48 96 20 40 60 80 100 1 1.5 2 4 6 8 10 12 24 48 96
mor t alit y (%) SF dose (g/ m3) Mean mor t alit y (% ± SE) of L. paet a adult s, nymphs, and eggs af t er 48 h of exposur e t o SF at var ious doses adult s nymphs eggs
Efficacy of sulfuryl fluoride for control of stored-product psocids
SLIDE 41 Dose to 100% kill of psocids after 48 h of exposure to SF
Dose (g/m3) Egg Nymph Adult Lepinotus reticulatus 24 4 8 Liposcelis bostrychophila
Liposcelis decolor 72
Liposcelis entomophila
4 Liposcelis paeta 96 6 6
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- Dr. Jim Campbell
- Insect Behavior
Movement of self-marked warehouse beetle males in a food facility shows for the first time how insects can move from one part
- f a facility to another to
reinfest after treatments, such as fumigation.
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- Dr. Jim Campbell
- Insect Behavior
Fumigation dates
Pest populations are being monitored in flour mills to determine the impact of fumigation treatments
- n the populations, and the
relationships between inside and
- utside populations with pheromone
trap capture and product infestation.
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- Dr. Brenda Oppert
- Insect proteomics
We are looking at protein profiles of insects and how to exploit those proteins for insect control.
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- Dr. Dick Beeman
- Insect genomics
The red flour beetle is the first agricultural pest to have its genome sequenced as a result of a collaboration between SPIRU, KSU, and the Baylor College of
that mining the genome will lead to totally new ways to control insect pests.
CHITIN SYNTHASE 2
LG5
marker cM
31.G5t 0.0
LG5
marker cM
31.G5t 0.0 51.7 35.B1s 32.O1s 36.I 1s 20C02 14A05 31.L5s
36.D10s 19.C3s 28.B16t 12E11 22.P3t 32.H2s PIG124 12C07 16B10 31.M1t 24.B1t 12G02 13G03 3F12 Txn049 PU123 32.H16s A81-2 43.9 40.1 44.5 44.5 45.2 46.8 46.0 46.0 46.0 46.0 46.8 48.1 46.8 53.4 50.4 51.7 49.8 49.8 54.0 54.0 51.7 54.0 51.7 27.P24t 51.7 C17A08 52.8 51.7 35.B1s 32.O1s 36.I 1s 20C02 14A05 31.L5s 36.D10s 19.C3s 28.B16t 12E11 22.P3t 32.H2s PIG124 PIG124 12C07 16B10 31.M1t 24.B1t 12G02 13G03 3F12 Txn049 PU123 PU123 32.H16s A81-2 43.9 40.1 44.5 44.5 45.2 46.8 46.0 46.0 46.0 46.0 46.8 48.1 46.8 53.4 50.4 51.7 49.8 49.8 54.0 54.0 51.7 54.0 51.7 27.P24t 51.7 C17A08 52.8
CHITIN SYNTHASE 1
cs1 46.8
CHITIN SYNTHASE 2
LG5
marker cM
31.G5t 0.0
LG5
marker cM
31.G5t 0.0 51.7 35.B1s 32.O1s 36.I 1s 20C02 14A05 31.L5s
36.D10s 19.C3s 28.B16t 12E11 22.P3t 32.H2s PIG124 12C07 16B10 31.M1t 24.B1t 12G02 13G03 3F12 Txn049 PU123 32.H16s A81-2 43.9 40.1 44.5 44.5 45.2 46.8 46.0 46.0 46.0 46.0 46.8 48.1 46.8 53.4 50.4 51.7 49.8 49.8 54.0 54.0 51.7 54.0 51.7 27.P24t 51.7 C17A08 52.8 51.7 35.B1s 32.O1s 36.I 1s 20C02 14A05 31.L5s 36.D10s 19.C3s 28.B16t 12E11 22.P3t 32.H2s PIG124 PIG124 12C07 16B10 31.M1t 24.B1t 12G02 13G03 3F12 Txn049 PU123 PU123 32.H16s A81-2 43.9 40.1 44.5 44.5 45.2 46.8 46.0 46.0 46.0 46.0 46.8 48.1 46.8 53.4 50.4 51.7 49.8 49.8 54.0 54.0 51.7 54.0 51.7 27.P24t 51.7 C17A08 52.8
LG5
marker cM
31.G5t 0.0
LG5
marker cM
31.G5t 0.0 51.7 35.B1s 32.O1s 36.I 1s 20C02 14A05 31.L5s
36.D10s 19.C3s 28.B16t 12E11 22.P3t 32.H2s PIG124 12C07 16B10 31.M1t 24.B1t 12G02 13G03 3F12 Txn049 PU123 32.H16s A81-2 43.9 40.1 44.5 44.5 45.2 46.8 46.0 46.0 46.0 46.0 46.8 48.1 46.8 53.4 50.4 51.7 49.8 49.8 54.0 54.0 51.7 54.0 51.7 27.P24t 51.7 C17A08 52.8 51.7 35.B1s 32.O1s 36.I 1s 20C02 14A05 31.L5s 36.D10s 19.C3s 28.B16t 12E11 22.P3t 32.H2s PIG124 PIG124 12C07 16B10 31.M1t 24.B1t 12G02 13G03 3F12 Txn049 PU123 PU123 32.H16s A81-2 43.9 40.1 44.5 44.5 45.2 46.8 46.0 46.0 46.0 46.0 46.8 48.1 46.8 53.4 50.4 51.7 49.8 49.8 54.0 54.0 51.7 54.0 51.7 27.P24t 51.7 C17A08 52.8
CHITIN SYNTHASE 1
cs1 46.8
SLIDE 46 Chitinase gene knockout by RNA inhibition (RNAi) normal
knocked out
Sixteen chitinase genes have been found via
shows results of inhibition of just one of these genes. The other 15 chitinases are still functional, yet the insect can’t molt and dies because it can’t digest the old cuticle, which therefore remains thick and stiff so the insect becomes entrapped when it tries to shed this
SLIDE 47 Cuticle cross-linking gene knocked out by RNAi
vacuum-pack de-aeration of food
There are 14 yellow genes involved in cuticle tanning and hardening. The cuticle-crosslinking gene yellow-e is required for waterproofing of the
- cuticle. Knockout of yellow-e results in loss of the waterproofing function of
the exoskeleton and in rapid desiccation and death. The insect becomes “vacuum-packed” in its own skin.
normal yellow-e gene knocked out
SLIDE 48 DNA fingerprinting for population/infestation analysis
individual #1 individual #2
Individual B differs from A at 2 positions out of 23 in this DNA segment. There are 6 million
- ther segments of this length in the genome.
DNA fingerprints
the same warehouse, showing 3 different genotypes, A, B & C
A A B B B C
SLIDE 49 to applied research from basic research SPIRU covers all areas
entomological research:
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Get further information and download publications at http://ars.usda.gov/npa/gmprc/spiru