Status of Pink Bollworm Resistance to Insecticides in Arizona

Total Page:16

File Type:pdf, Size:1020Kb

Status of Pink Bollworm Resistance to Insecticides in Arizona Status of Pink Bollworm Resistance to Insecticides in Arizona Item Type text; Article Authors Watson, Theo F.; Kelly, Suzanne E. Publisher College of Agriculture, University of Arizona (Tucson, AZ) Journal Cotton: A College of Agriculture Report Download date 30/09/2021 21:22:12 Link to Item http://hdl.handle.net/10150/208371 Status of Pink Bollworm Resistance To Insecticidesin Arizona Theo F. Watson and Suzanne E. Kelly Abstract Populations of pink bollworm. Pectinophora gossypiella (Saunders), from Yuma, Casa Grande, Marana and Safford were compared with that of a susceptible laboratory (USDA) strain relative to their susceptibility to permethrin. A limited comparison was made with azinphosmethyl. All field strains were significantly more tolerant to permethrin than was the USDA susceptible strain. A comparison of the USDA and Yuma strains using azinphosmethyl indicated no difference in susceptibility between the laboratory and field strains. Introduction The pink bollworm, Pectinophora gossypiella (Saunders), has been a pest of cotton in Arizona since 1926, but only causing serious economic losses from 1965, after completing its spread across Arizona and southern California (Watson and Fullerton 1969). Since 1966 insecticides have been routinely used to effectively control this pest and prevent serious yield losses. In 1977, the synthetic pvrethroids were introduced into the cotton pest control scheme to control outbreaks of Heliothi.s spp., primarily tobacco budworm, H. virescerts (F.), which was resistant to the other classes of insecticides. The pyrethroids were also very effective against the pink bollworm and were therefore used extensively for control of this pest as well. In the mid- 1980's reports began to appear showing resistance in the pink bollworm to this class of insecticides (Bariola 1985, Haynes et al. 1986). Osman et al. (1991) conducted a study in 1986 which showed that variability in response to permethrin existed among field strains but that at least two populations (Yuma and Phoenix) exhibited levels of resistance comparable to that found in the Westmoreland, CA strain, the original site where resistance was observed. Response of all field populations to azinphosmethyl was similar and little different from the susceptible laboratory strain. As a result of extremely high populations of pink bollworm in many areas of Arizona in 1990, and difficulty in controlling them in certain areas, a re- assessment of pyrethroid efficacy was undertaken. Infested bolls were collected in late Fall from Parker, Yuma, Casa Grande, Marana and Safford from which emerging pink bollworms were obtained for the comparative studies with the USDA susceptible strain. The Parker collection failed to yield sufficient numbers from which meaningful data could be obtained and therefore is not included in this report. Methods Pink bollworm -infested bolls were collected from Parker, Yuma, Casa Grande, Marana and Safford, and returned to the University of Arizona Entomology Laboratory at the Campus Agricultural Center (CAC) for collection of moths for resistance assessment. The susceptible strain used for comparison 154 was obtained from the Western CottonResearch Laboratory, USDA -ARS, Phoenix, Arizona. The infested bolls were placed on screened trays on greenhouse benches andlined with paper towels as pupation sites for emerging larvae. These were periodically collectedand held in 230m1 paper ice cream cups for moth emergence. Laterthese bolls were placed in small pyramidal pink bollworm emergence cages and moths collecteddaily from the collection site at the apex of the cages. Adults were anaesthetized with carbon dioxide and treatedindividually with 1 pi of the test solution applied to the dorsum. The topical application was donewith a motor -driven micro -applicator fitted with a 0.25m1 tuberculin syringe. Treated insects were held inrearing cups and provided with a 10% sugar solution for food. Mortality counts weremade at 24 and 48 hours after treatment. Results Figure I shows the relative tolerance of 4 field strains of pink bollworm(PBW) to permethrin when compared with the USDA strain. Populations from Casa Grande,Marana and Yuma had LD50's (lethal dose of insecticide to kill 50% of the population) severalfold higher than the USDA strain, while the Safford population was intermediate but still much harder tokill than the susceptible strain(USDA). Figure 2 compares the change in LD50's with permethrin from1986 (Osman et al. 1991) to 1990 for populations from Safford, Marana and Yuma. Susceptibilitydropped slightly in the USDA and Yuma populations while increasing significantly for those at Maranaand Safford. Figure 3 shows a comparison in response to permethrin between1986 and 1990 for 3 specific insecticide concentrations for PBW populations from Safford,Marana and Yuma. The vertical bars represent percent mortality and show essentiallythe same relationship as in figure 2, i.e., a lower mortality in 1990 at all concentrations for populations fromSafford and Marana but higher mortality in the Yuma population. Figure 4 shows the tolerance levels for azinphosmethyl for bothtesting periods for the USDA and Fuma populations. There was no change between 1986 and1990 in the USDA strain but some increased susceptibility in the Yuma strain was evident. In summary, there was an increased tolerance to permethrinfor PBW populations in central and eastern Arizona. In western Arizona there was somedecline in tolerance to permethrin but the level was still sufficiently high to portendproblems with control. There was no indication of tolerance to azinphosmethyl developing in field populations. References Cited Bariola, L. A. 1985. Evidence of resistance to syntheticpyrethroids in field populations of pink bollworm in southern California. p. 138. Lg. proceedings ofthe beltwide cotton production and research conference, Jan. 6 -11, 1985. New Orleans, LA. Haynes, K. F., T. A. Miller, R. T. Staten, W. G. Li, andT. C. Baker. 1986. Monitoring insecticide resistance with insect pheromones. Experimentia 42: 1293 -1295. Osman, A. A., T. F. Watson and S. Sivasupramiam. 1991.Susceptibility of field populations of pink bollworm (Lepidoptera: Gelechiidae)to azinphosmethyl and permethrin and synergism of permethrin. J. Econ. Entomol. (in press). Watson, T. F. and D. G. Fullerton. 1989. Timing of insecticidalapplications for control of pink bollworm. J. Econ. Entomol. 62: 682 -685. 155 4-7 USDA Casa Marana Safford Yuma Grande STRAIN Figure 1. Permethrin tolerance of pink bollworm from various locations inArizona in 1990, compared to a susceptible (USDA) strain. 18= Permethrin 16-' 1986 .111 14-' AMMO, 1990 -.MAW p)121 CY) 10- O _, 6-' 2-' ,...._. AIM 4=Prilk\s, 0 -el& \USDA MARANA SAFFORD YU MA STRAIN Figure 2. Change in tolerance to permethrin between 1986 and 1990 of pink bollworm strainsfrom various locations in Arizona, compared to a susceptible (USDA) strain. 156 100 90 1986 80 1990 70 60 50 40 30 20 10 0 MARANA SAFFORD YUMA STRAIN 100 0.12 ug/moth 90-' \.. 1986 80 .wrr 1990 70~' \ 60 \ 50 40-' 30-¡ 20- 10-' o _\\ MARANA SAFFC'9D YUMA STRAIN 100 90 1986 80 Ell 1990 70 60 50 40 30 20 10 0 MARANA SAFFORD YUMA STRAIN Figure 3. Susceptibility to pernlethrin in1986 and 1990 at concentrations of 0.08, 0.12 and0.16 jig /A13\\' moth, for strainsfrom Safford, Marana and Yuma. 157 Azinphosmethyl 1986 1990 USDA YUMA STRAIN Figure 4. Change in tolerance to azinphosmethyl between 1986 and 1990 of apink bollworm strain from Yuma, Arizona, compared to a susceptible (USDA) strain. 158.
Recommended publications
  • Entomology) 1968, Ph.D
    RING T. CARDÉ a. Professional Preparation Tufts University B.S. (Biology), 1966 Cornell University M.S. (Entomology) 1968, Ph.D. (Entomology) 1971 New York State Agricultural Postdoctoral Associate, 1971-1975 Experiment Station at Geneva (Cornell University) b. Appointments and Professional Activities Positions Held 1996-present Distinguished Professor & Alfred M. Boyce Endowed Chair in Entomology, University of California, Riverside 2011 Visiting Professor, Swedish Agricultural University (SLU), Alnarp 2003-2009 Chair, Department of Entomology, University of California, Riverside 1989-1996 Distinguished University Professor, University of Massachusetts 1988 Visiting Scientist, Wageningen University 1984-1989 Professor of Entomology, University of Massachusetts 1981-1987; 1993-1995 Head, Entomology, University of Massachusetts 1981-1984 Associate Professor of Entomology, University of Massachusetts 1978-1981 Associate Professor of Entomology, Michigan State University 1975-1978 Assistant Professor of Entomology, Michigan State University Honors and Awards (selected) Certificate of Distinction for Outstanding Achievements, International Congress of Entomology, 2016 President, International Society of Chemical Ecology, 2012-2013 Jan Löfqvist Grant, Royal Academy of Natural Sciences, Medicine and Technology, Sweden, 2011 Silver Medal, International Society of Chemical Ecology, 2009 Awards for “Encyclopedia of Insects” include: • “Most Outstanding Single-Volume Reference in Science”, Association of American Publishers 2003 • “Outstanding
    [Show full text]
  • A Review of Sampling and Monitoring Methods for Beneficial Arthropods
    insects Review A Review of Sampling and Monitoring Methods for Beneficial Arthropods in Agroecosystems Kenneth W. McCravy Department of Biological Sciences, Western Illinois University, 1 University Circle, Macomb, IL 61455, USA; [email protected]; Tel.: +1-309-298-2160 Received: 12 September 2018; Accepted: 19 November 2018; Published: 23 November 2018 Abstract: Beneficial arthropods provide many important ecosystem services. In agroecosystems, pollination and control of crop pests provide benefits worth billions of dollars annually. Effective sampling and monitoring of these beneficial arthropods is essential for ensuring their short- and long-term viability and effectiveness. There are numerous methods available for sampling beneficial arthropods in a variety of habitats, and these methods can vary in efficiency and effectiveness. In this paper I review active and passive sampling methods for non-Apis bees and arthropod natural enemies of agricultural pests, including methods for sampling flying insects, arthropods on vegetation and in soil and litter environments, and estimation of predation and parasitism rates. Sample sizes, lethal sampling, and the potential usefulness of bycatch are also discussed. Keywords: sampling methodology; bee monitoring; beneficial arthropods; natural enemy monitoring; vane traps; Malaise traps; bowl traps; pitfall traps; insect netting; epigeic arthropod sampling 1. Introduction To sustainably use the Earth’s resources for our benefit, it is essential that we understand the ecology of human-altered systems and the organisms that inhabit them. Agroecosystems include agricultural activities plus living and nonliving components that interact with these activities in a variety of ways. Beneficial arthropods, such as pollinators of crops and natural enemies of arthropod pests and weeds, play important roles in the economic and ecological success of agroecosystems.
    [Show full text]
  • Use of Pheromones for Pink Bollworm (Pectinophora Gossypiella, Saunders) Mating Disruption in Israel A
    A. Niv Use of Pheromones for Pink Bollworm (Pectinophora gossypiella, Saunders) Mating Disruption in Israel A. Niv The Cotton Production and Marketing Board, Israel, P.O.Box 384, Herzlia B. Israel. ABSTRACT Pink bollworm (Pectinophora gossypiella) is one of the major cotton pests of Israel. Until ten years ago the pest appeared mainly in one region, the Beit-Shean valley, but it has spread all over Israel. The number of spray applications against this pest ranges between 1 and 9, mainly organo-phosphates and pyrethroids. Applications start early in the season, disrupting the delicate balance that exists between natural enemies and pests. The result is severe outbreaks of other pest. In the mid-1980s, the Sandoz pheromone product “No Mate” was used for mating disruption. P.B. Rope technology evolved in the Beit Shean valley during the 1990’s. The average number of insecticide sprays declined from 9 to 5. Insecticide applications only commenced in the middle of the season following delayed pink bollworm occurrence and the decline in population intensity. This affected other pest populations. Since 1991 the use of P.B. Ropes and P.B. Rings (AGRISENSE) has increased and during the 1998 season, approximately half the cotton fields are treated with P.B. Ropes. The recommendation in Israel is to administer pheromone Ropes and rings early in the season, prior to appearance of pin-head squares. The initial dosage used to be 500 units (50 mg) per hectare but has been reduced to 250 (40 mg) units per hectare. The application of the pheromones is manual and time consuming.
    [Show full text]
  • Pectinophora Gossypiella (Saunders)
    Keys About Fact Sheets Glossary Larval Morphology References << Previous fact sheet Next fact sheet >> GELECHIIDAE - Pectinophora gossypiella (Saunders) Taxonomy Click here to download this Fact Sheet as a printable PDF Gelechioidea: Gelechiidae: Pexicopiinae: Pectinophora gossypiella (Saunders) Common names: pink bollworm Synonyms: Gelechia umbripennis Larval diagnosis (Summary) Fig. 1: Late instar, lateral view Adfrontal setae are widely separated and AF2 is at the apex of the front Mandible with four teeth, the last one smaller than the others Crescent shaped marking often present on the prothoracic shield Abdominal prolegs with crochets in a uniordinal penellipse Anal crochets in a single uninterrupted band SD1 on A9 is setaform, not hairlike Fig. 2: Late instar, lateral view SD1 on A8 is dorsad to the spiracle Host/origin information The pink bollworm is most commonly intercepted on okra (Abelmoschus esculentus) originating from the Caribbean. More than 89% of all interceptions are from Haiti. Origin Host(s) Haiti Abelmoschus esculentus Fig. 3: T1 shield Recorded distribution Pectinophora gossypiella is distributed in scattered locations throughout southern Europe, Africa, the Middle East, Asia, and Australia. In the New World it occurs from the southern U.S. to Argentina, including the Caribbean (Gall 1966, Hill 1975). Identifcation authority (Summary) It is important to restrict identifications of P. gossypiella to the proper hosts and known distribution. Pectinophora gossypiella feeds on Malvaceae and has been recorded from the Fig. 4: Abd. crochets Fig. 5: Anal crochets locations listed above. Many of the exotic species related to the pink bollworm, although not common at ports, represent a serious threat to North American agriculture.
    [Show full text]
  • Volatile DMNT Directly Protects Plants Against Plutella Xylostella By
    RESEARCH ARTICLE Volatile DMNT directly protects plants against Plutella xylostella by disrupting the peritrophic matrix barrier in insect midgut Chen Chen1†, Hongyi Chen1†, Shijie Huang1†, Taoshan Jiang1, Chuanhong Wang1, Zhen Tao1, Chen He1, Qingfeng Tang2, Peijin Li1* 1The National Key Engineering Lab of Crop Stress Resistance Breeding, the School of Life Sciences, Anhui Agricultural University, Hefei, China; 2Key Laboratory of Biology and Sustainable Management of Plant Diseases and Pests of Anhui Higher Education Institutes, the School of Plant Protection, Anhui Agricultural University, Hefei, China Abstract Insect pests negatively affect crop quality and yield; identifying new methods to protect crops against insects therefore has important agricultural applications. Our analysis of transgenic Arabidopsis thaliana plants showed that overexpression of pentacyclic triterpene synthase 1, encoding the key biosynthetic enzyme for the natural plant product (3E)-4,8-dimethyl- 1,3,7-nonatriene (DMNT), led to a significant resistance against a major insect pest, Plutella xylostella. DMNT treatment severely damaged the peritrophic matrix (PM), a physical barrier isolating food and pathogens from the midgut wall cells. DMNT repressed the expression of PxMucin in midgut cells, and knocking down PxMucin resulted in PM rupture and P. xylostella death. A 16S RNA survey revealed that DMNT significantly disrupted midgut microbiota *For correspondence: populations and that midgut microbes were essential for DMNT-induced killing. Therefore, we [email protected] propose that the midgut microbiota assists DMNT in killing P. xylostella. These findings may †These authors contributed provide a novel approach for plant protection against P. xylostella. equally to this work Competing interests: The authors declare that no Introduction competing interests exist.
    [Show full text]
  • Gelechiidae Biosecurity Occurrence Background Subfamilies Short
    Ardozyga stratifera (Gelechiinae) Gelechiidae Twirler Moths or Gelechiid Moths Biosecurity BIOSECURITY ALERT This Family is of Biosecurity Concern Occurrence This family occurs in Australia. Background The micromoth family Gelechiidae is the namesake family for the enormous superfamily Gelechioidea and is one of the most diverse families of the Lepidoptera. Gelechiids are very small moths with narrow wings. The family has a worldwide distribution and is diverse with over 4,700 known species in 500 genera, but that number would be at least doubled with undescribed and new species. The family is particularly prevalent in North America because of the close association of species with Douglas fir (Pseudotsuga). The caterpillars have very diverse feeding habits on many plant parts and species. Many species are external feeders but are protected by a shelter of some kind, often in tied or rolled leaves (Fig. 1). Many others feed internally, boring into flower heads, stems (Fig. 2) or roots. They are leaf-miners (Fig. 11), gall-inducers or stem-borers, or feed within flowers or fruits (Fig. 13). They also can be concealed in silken tunnels in earth or in portable cases. Not surprisingly, therefore, there are many gelechiids that are agricultural pests, such as: the pink bollworm, Pectinophora gossypiella (Fig. 13), one of the most destructive pests of cotton in the world; Sitotroga cerealella (Angoumois grain moth); Phthorimaea operculella (potato tuber moth); and, Tuta absoluta (tomato leaf miner). Contrastingly, several species have been used as biocontrol agents against weeds. One Australian species feeds on dead leaf litter. Fig. 1. Mature caterpillar of the widespread Australian gelechiid Ardozyga stratifera (Gelechiinae).
    [Show full text]
  • Transgenic Cotton and Sterile Insect Releases Synergize Eradication of Pink Bollworm a Century After It Invaded the United States
    Transgenic cotton and sterile insect releases synergize eradication of pink bollworm a century after it invaded the United States Bruce E. Tabashnika,1, Leighton R. Liesnerb, Peter C. Ellsworthc, Gopalan C. Unnithana, Jeffrey A. Fabrickd, Steven E. Naranjod, Xianchun Lia, Timothy J. Dennehya,2, Larry Antillab, Robert T. Statene, and Yves Carrièrea aDepartment of Entomology, University of Arizona, Tucson, AZ 85721; bArizona Cotton Research and Protection Council, Phoenix, AZ 85040; cDepartment of Entomology, University of Arizona, Maricopa, AZ 85138; dUS Arid Land Agricultural Research Center, Agricultural Research Service, US Department of Agriculture, Maricopa, AZ 85138; and eAnimal and Plant Health Inspection Service, US Department of Agriculture, Phoenix, AZ 85040 Edited by David Denlinger, The Ohio State University, Columbus, OH, and approved November 20, 2020 (received for review September 10, 2020) Invasive organisms pose a global threat and are exceptionally Transgenic Bt cotton helped to reduce the total annual cost of pink difficult to eradicate after they become abundant in their new bollworm damage and insecticide treatments to $32 million in the habitats. We report a successful multitactic strategy for combating United States (18). Although Bt cotton kills essentially 100% of the pink bollworm (Pectinophora gossypiella), one of the world’s susceptible pink bollworm larvae (19–21), this pest rapidly evolved most invasive pests. A coordinated program in the southwestern resistance to Bt proteins in laboratory selection experiments in United States and northern Mexico included releases of billions of ArizonaandinBtcottonfieldsinIndia(20–24). To delay the sterile pink bollworm moths from airplanes and planting of cotton evolution of resistance to Bt cotton, farmers in Arizona planted engineered to produce insecticidal proteins from the bacterium “refuges” of non-Bt cotton that yielded abundant susceptible moths Bacillus thuringiensis (Bt).
    [Show full text]
  • Biological Parameters of Pink Bollworm Pectinophora Gossypiella (Saunders) (Lepidoptera:Gelechiidae): a Looming Threat for Cotton and Its Eradication Opportunity
    International Journal of Research in Agriculture and Forestry Volume 4, Issue 7, 2017, PP 25-36 ISSN 2394-5907 (Print) & ISSN 2394-5915 (Online) Biological Parameters of Pink Bollworm pectinophora gossypiella (Saunders) (Lepidoptera:Gelechiidae): A looming Threat for Cotton and its Eradication Opportunity Muhammad Sarwar Nuclear Institute for Agriculture & Biology (NIAB), Faisalabad-38950, Punjab, Pakistan *Corresponding Author: Muhammad Sarwar, Nuclear Institute for Agriculture & Biology (NIAB), Faisalabad-38950, Punjab, Pakistan Received Date: 11-08-2017 Accepted Date: 04-09-2017 Published Date: 05-09-2017 ABSTRACT Pink bollworm Pectinophora gossypiella (Saunders) (Lepidoptera: Gelechiidae), is a worldwide key pest of cotton and its larvae burrow into cotton bolls to feed on the seeds. Early in the season, eggs are laid in any of the sheltered places of the plant axis of petioles or peduncles, the underside of young leaves and on buds or flowers. Once the bolls are 15 days old, these become favored sites for adult’s oviposition. First two larval instars are white, while from third instar pink color develops and lint of pink bollworm attacked bolls is of inferior quality. The feeding damage allows other insects and fungi to enter the boll and cause additional damage. When the larva exits from the cotton boll, it leaves a perfectly round and clean cut exit hole which is diagnostic of pink bollworm damage. Cultural control plays a key role in keeping down the number of pink bollworm carry-over between cotton crops. Maintenance of host free period during off- season is an essential option to ensure a pink bollworm free next cotton season.
    [Show full text]
  • SIT Glossary
    GLOSSARY Definitions of selected words and phrases in the subject index of Sterile Insect Technique Principles and Practice in Area-Wide Integrated Pest Management Published by Springer in 2005 Term Definition A aberration Any body, form (shape) or structure that deviates from the normal or typical condition (Gordh and Headrick 2001). A form that departs in some striking way from the normal type, occurring either singly, or rarely, at irregular intervals (Torre-Bueno 1978). See ‗chromosomal aberration‘. absolute density Density of a population expressed as an absolute number per ground-surface area or per unit of volume (Pedigo 2002). Density of a population expressed as every individual of a population within a volume of habitat [paraphrased] (Daly et al. 1998). Contrasts with the relative density of a population expressed as a relative number based on the kind of sampling technique used, e.g. number caught in a trap (Pedigo 2002). See ‗apparent density‘, ‗Lincoln Index‘. absorbed dose Quantity of radiating energy (in gray) absorbed per unit of mass of a specified target (FAO 2006). Quantity of ionizing radiation energy imparted per unit mass of a specified material. The SI [International System of Units] unit of absorbed dose is the gray (Gy), where 1 gray is equivalent to the absorption of 1 joule per kilogram of the specified material (1 Gy = 1 J / kg). The mathematical relationship is the quotient (D) of d by dm, where d is the mean incremental energy imparted by ionizing radiation to matter of incremental mass dm. The discontinued unit for absorbed dose is the rad (1 rad = 100 erg / g = 0.01 Gy).
    [Show full text]
  • A Brief History of Helicoverpa and Pectinophora
    A Brief History of Helicoverpa and Pectinophora Derek Russell Faculty of Veterinary and Agricultural Sciences University of Melbourne Where did Pink bollworm come from? Early recorded distrib. closely related to perennial G. arboreum Family: Gelechidae c. 3,000 sps Other Pectinophora species in Australia e.g. pink spotted bollworm P. scutigera (pests of cotton but primary hosts Hibiscus tiliaceus and Thespesia polulnea Possible origin ex Australia via Azana (=Thespesia) lampas G.hirsutum through Philippines to and populnea India where Thepesia lampas was a major wild host Pink bollworm dispersal in cotton seed Pest (in India) only after 1840 -intro. of American Upland cottons in 1790 Ist description 1843 from India as Platyedra by Saunders 5 - other sps in Europe, Turkestan, Iran, 4 3 Morocco as cotton pests 2 1 Pectinophora – Busck in 1917 4 (The pink bollworm J.Ag. Res 9: 343-370) 1. Australia to India via Phillipines (on G. arboreum) Date??? 2. India to W.Africa1. Australia1904 (on to India G.arboreum via Philippines) date? 3. India to Ceylon, Burma and Egypt 1906 and Hawaii 1911. Hawaii – W. Indies 1911 4. Egypt to Mexico and Brazil 1913-16 5. Mexico to USA c.1916 India (???) to China 1918 P. gossypiella – current distribution Hosts: Malvacae Wild Gossypium and Althaea sps. (Hollyhocks ) Cultivated Abelmoschus esculentus (Okra) Countries: Abutilion sps, Hibiscus sps. and Asia -29 cotton sps. Africa - 35 North America – 2 Fabeacae Central America - 20 Cultivated South America - 9 Midicago sativa (Lucerne) Europe - 11 Data: CABI PlantWise Oceanea - 8 Destruction of cotton production by Pink bollworm Sometimes with other sps – esp.
    [Show full text]
  • Pectinophora Gossypiella
    Pectinophora gossypiella Scientific Name Pectinophora gossypiella Saunders Synonyms: Depressaria gossypiella Saunders Ephestia gossypiella Saunders Gelechia gossypiella Saunders Gelechiella gossypiella Saunders Platyedra gossypiella Saunders Common Name(s) Pink bollworm Figure 1. P. gossypiella larvae. Image Type of Pest courtesy of Peggy Greb, USDA Agricultural Moth Research Service, www.bugwood.org. Taxonomic Position Class: Insecta, Order: Lepidoptera, Family: Gelechiidae Reason for Inclusion In Manual PPQ Program Pest Pest Description Eggs: Elongate oval, flattened; about 1 mm long and 0.5 mm broad (0.04 by 0.02 in.); the shell is pearly white, with a finely wrinkled surface. When newly laid, the egg has a slightly greenish tint. At maturity it turns reddish (Busck, 1917). Larvae: The larvae (Fig. 1) are initially white with a dark head. The full grown larvae are Figure 2. P. gossypiella adult. Image 10 to 12 mm (0.39 to 0.47 in.) long and are courtesy of Mississippi State University white with a double red band on the upper Archive, Mississippi State University, portion of each segment (Mukuka et al., www.bugwood.org. 2002). Pupae: The pupa is 8 to 10 mm (0.31 to 0.39 in.) long, rather plump, reddish brown; posterior end pointed and terminating in a short, stout, upwardly turned hooklike cremaster; entire surface finely pubescent; no long setae, spines or hooks, except on last joint. When mature, the pupa becomes much darker; the imago's eyes can be seen prominently under the gena of the pupal skin, and the segmentation of the adult antennae and legs becomes discernible (Busck, 1917). 1 Adults: Moths (Fig.
    [Show full text]
  • Novel RNA Viruses from the Transcriptome of Pheromone Glands in the Pink Bollworm Moth, Pectinophora Gossypiella
    insects Article Novel RNA Viruses from the Transcriptome of Pheromone Glands in the Pink Bollworm Moth, Pectinophora gossypiella Xiaoyi Dou 1, Sijun Liu 1,*, Victoria Soroker 2, Ally Harari 2 and Russell Jurenka 1 1 Department of Entomology, Iowa State University, Ames, IA 50011, USA; [email protected] (X.D.); [email protected] (R.J.) 2 The Volcani Center, Institute of Plant Protection, ARO, Bet-Dagan 50250, Israel; [email protected] (V.S.); [email protected] (A.H.) * Correspondence: [email protected] Simple Summary: The pink bollworm, Pectinophora gossypiella (Lepidoptera: Gelechiidae), is a major pest of cotton. In this study, we analyzed the mRNA from pheromone glands of two populations in Israel. We found several virus sequences that were the same in these populations. We identified these viruses based on high-throughput sequencing data and analysis of the assembled transcripts. Through analysis of the sequences, we identified several unique viral sequences representing possible novel viral species. Two of the viral sequences were found in relatively high abundance in pheromone glands. One of the virus sequences was also found through analysis of previous transcriptome sequencing data from the midgut of pink bollworm larvae. This is the first report of these unique viral sequences found in the pink bollworm, and these viruses could be developed to help control this pest around the world, but more research is needed to determine their utility as biological control agents. Citation: Dou, X.; Liu, S.; Soroker, V.; Harari, A.; Jurenka, R. Novel RNA Abstract: In this study, we analyzed the transcriptome obtained from the pheromone gland iso- Viruses from the Transcriptome of lated from two Israeli populations of the pink bollworm Pectinophora gossypiella to identify viral Pheromone Glands in the Pink sequences.
    [Show full text]