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Potato Tuberworm Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae)

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EENY587
Potato Tuberworm Phthorimaea operculella (Zeller)
(Lepidoptera: Gelechiidae)1
Harsimran K. Gill, Gurminder Chahil, Gaurav Goyal, Arshdeep K. Gill, and Jennifer L.
Gillett-Kaufman2
1. This document is EENY587, one of a series of the Entomology and Nematology Department, UF/IFAS Extension. Original publication date February
2014. Visit the EDIS website at http://edis.ifas.u.edu.
2. Harsimran K. Gill, post doctoral research associate, Entomology and Nematology Department; Gurminder Chahil, Dalhousie University, NS, Canada;
Gaurav Goyal, post doctoral research associate, Department of Entomology, Punjab Agricultural University, India; Arshdeep Gill, Department of
Entomology, Punjab Agricultural University, India; and Jennifer L. Gillett-Kaufman, associate extension scientist, Entomology and Nematology
Department, UF/IFAS Extension, Gainesville, FL 32611.
The Institute of Food and Agricultural Sciences (IFAS) is an Equal Opportunity Institution authorized to provide research, educational information and other services
only to individuals and institutions that function with non-discrimination with respect to race, creed, color, religion, age, disability, sex, sexual orientation, marital status,
national origin, political opinions or aliations. For more information on obtaining other UF/IFAS Extension publications, contact your county’s UF/IFAS Extension oce.
U.S. Department of Agriculture, UF/IFAS Extension Service, University of Florida, IFAS, Florida A & M University Cooperative Extension Program, and Boards of County
Commissioners Cooperating. Nick T. Place, dean for UF/IFAS Extension.
Introduction
e potato tuberworm Phthorimaea operculella (Zeller),
also known as potato tuber moth or tobacco splitworm,
is an oligophagous pest (an insect feeding on a restricted
range of food plants) of crops belonging to the family
Solanaceae (mainly potatoes [Solanum tuberosum L.],
tomatoes [Solanum lycopersicum L.] and tobacco [Nicotiana
tabacum L.]). Phthorimaea operculella has been a minor
pest of tobacco for more than 100 years. However, in
North Carolina, this pest has emerged as a problem in
tobacco plantings over the last ve years. is pest has been
reported in tropical, subtropical and Mediterranean agro-
zones (Westedt et al. 1998, Flanders et al. 1999, Visser 2005,
Golizadeh and Esmaeili 2012).
e potato tuberworm aects production, reduces quality
of the produce and increases the risk of infection by plant
pathogens. e common name potato tuberworm is
given to its damaging larval stage. ere are two species
in dierent genera with similar names: Tecia solanivora
(Povolny) and Symmetrischema tangolias (Gyen). Tecia
solanivora (Povolny), the Guatemalan potato moth, is
found in Central America and northern South America and
attacks potatoes that are still in the eld as well as stored
potatoes. e Andean or South American potato tuber
moth, Symmetrischema tangolias (Gyen), is a pest of stored
potatoes in the Andes.
Distribution
Potato tuberworm is a cosmopolitan pest. In the United
States it has been reported in at least 25 states from the
Atlantic to the Pacic coast. is pest occurs in most areas
where potatoes or other solanaceous plants are grown.
It was rst recorded in California in 1856 (Alvarez et al.
2005). However, it was not a major concern for growers
Figure 1. Damage on a potato inicted by the potato tuberworm,
Phthorimaea operculella
(Zeller).
Credits: Silvia I. Rondon, Hermiston Agricultural Research and
Extension Center, Oregon State University.
2
Potato Tuberworm Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae)
in the Pacic Northwest until 2002, when severe potato
tuberworm damage was documented in a eld near Herm-
iston, Oregon (Rondon et al. 2007). It occurs widely in
Africa (Ethiopia, Egypt, Kenya), Asia (Iran, Syria), Europe,
Americas (Latin America, Andes of Peru and Bolivia) and
Oceania (Australia and New Zealand) (Saour 2004, Vargas
et al. 2004, Davidson et al. 2006, Golizadeh and Esmaeili
2012, Golizadeh and Zalucki 2012, Ahmed et al. 2013,
Kroschel et al. 2013). Potato tuberworm has been reported
in more than 90 countries (Anonymous 2013).
Host Range
Potato tuberworms are mainly associated with potatoes;
however, they have been observed feeding on other plants,
such as tomatoes, eggplants (Solanum melongena L.),
peppers (Capsicum spp.), tobacco and wild solanaceous
plants like Jimson weed or datura (Datura stramonium
L.) (Alvarez et al. 2005). In the Pacic northwest, potato
tuberworms have only been reported infesting potatoes
(Rondon et al. 2007).
Life History
Eggs, larvae and pupae of potato tuberworm can potentially
survive in volunteer potatoes, or in the soil aer harvest.
Potato tuberworm is known to survive in the soil as pupae.
Larval development is interrupted by temperatures below
50°F. Larvae can pupate in the soil, discarded piles of
potatoes, dead leaves, on storage walls, or on eyes of stored
tubers (Raman 1980). ey can also pupate in crevices in
walls, oors and crates.
All instars may occur together in overlapping generations.
ere are two to eight generations per year depending upon
climatic conditions. ere are usually two generations per
year in temperate climates of North America (Alvarez et al.
2005). In the Northern Hemisphere, peak populations of
adults occur from May through June in Israel, from June
through August in Yemen, and from April to October in the
United States. Generation time can vary from two weeks
during summer to seven or eight months if the cycle is
interrupted by winter. Winter populations can be active in
storage facilities where optimum temperature for survival is
maintained. Potato tuber moths can move up to 0.15 miles
between crops to infest plants or tubers. Long distance
movement of potato tuberworms occurs when infested
tubers are accidentally transported (Alvarez et al. 2005).
Eggs
When foliage is not available, potato tuberworm moths can
crawl short distances through cracks in loose soil to nd
a tuber they will use as an oviposition site. In four days,
the adult female can deposit 60 to 200 eggs singly or in
small clusters directly on host plant parts such as the stem,
underside of leaves, or in the eye cracks and indentations
on tubers. Eggs are smooth, oval, and can be pearly white to
yellowish (before hatching) in color. e eggs usually hatch
aer ve days.
Larvae
Larvae are 0.5 to 0.6 inch long, white or yellow with a
brown head andprothorax (midsection of the insect body)
(Raman 1980, Alvarez et al. 2005). e thorax has small
black points and bristles on each segment. e color of
larvae changes from white or yellow to pink or green as
they mature. e larvae feed on their host plants for up to
two weeks before pupation.
Figure 2. Larva of the potato tuberworm,
Phthorimaea operculella
(Zeller).
Credits: Oregon State University Extension.
Figure 3. Leaf mines caused by the potato tuberworm,
Phthorimaea
operculella
(Zeller).
Credits: Silvia I. Rondon, Hermiston Agricultural Research and
Extension Center, Oregon State University.
3
Potato Tuberworm Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae)
Pupa
Pupae are white, narrow and 0.5 inch long. Depending
upon climatic conditions, pupae take 10 to 30 days to fully
develop (Raman 1980, Alvarez et al. 2005). e silken
cocoon spun around pupae can become covered with soil
and debris.
Adults
e moths are narrow bodied, silver grey in color, 0.4 inch
long with a wing span of 0.5 inch. Wings are grayish-brown,
fringed and elongate with small brown or black markings.
Both pairs of wings have fringed edges. At rest, the wings
are held close to the body, giving the moth a slender
appearance. e forewings are yellowish grey with dark
spots (2-3 dots on males and characteristic “X” pattern on
females); the hind wings are grey (Raman 1980, Alvarez et
al. 2005).
e adults are fast iers and like most other moths require
an insect-collecting net for capturing. ese moths live
for one to two weeks, are crepuscular (active at dawn and
dusk), and feed on nectar. Females are slightly larger than
males. Mating begins 24 hours aer emergence.
Damage
Larvae feed on potato leaves, stems, petioles, and, more
importantly, potato tubers in the eld and in storage. e
newly hatched larvae create mines on leaves by feeding on
leaf tissue while leaving the upper and lower epidermis
of the leaf intact. ey prefer feeding on young foliage
(Trivedi and Rajagopal 1992). Typical damage results from
larvae boring tunnels in tubers. Larvae depositing their
excreta make tubers unt for consumption. Potato tuber
eyes become pink due to deposition of silk and excrement
by potato tuberworm infestation. Severe infestations result
in yield and quality losses during storage where previously
infested tubers are stored with healthy potato tubers
(Malakar and Tingey 2006, Rondon 2010). is generally
destroys the entire crop of stored potatoes.
Most economic damage occurs to potato tubers in storage
conditions in developing countries and is caused by larval
feeding. Presence of even one larva is sucient to spoil and
destroy a tuber. Rapidly moving caterpillars penetrate the
tubers, form galleries coated with silken threads and eject
frass outside the tuber. On leaves, caterpillars form galleries
and then penetrate other plant parts. Aer two to three
weeks, caterpillars leave the plant (caterpillars can move
through cracks in soil) and pupate on walls of potato bags
Figure 4. Late larval instars and pupae of the potato tuberworm,
Phthorimaea operculella
(Zeller) on a damaged potato.
Credits: Silvia I. Rondon, Hermiston Agricultural Research and
Extension Center, Oregon State University.
Figure 5. The potato tuberworm,
Phthorimaea operculella (Zeller)
adults. The forewings have 2-3 dark spots on males (right), and a
characteristic “X” pattern on females (left).
Credits: Silvia I. Rondon, Hermiston Agricultural Research and
Extension Center, Oregon State University.
Figure 6. Damage on potato tuber caused by
Phthorimaea operculella
(Zeller).
Credits: Silvia I. Rondon, Hermiston Agricultural Research and
Extension Center, Oregon State University.
4
Potato Tuberworm Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae)
lying in potato elds. Fungi, bacteria and mites can develop
inside the tunnels made by the larvae, which causes the
tubers to rot and emit an unpleasant smell.
Stored crop losses in potatoes ranging from 50% in Yemen
and Peru; 86% in Tunisia, Algeria and Turkey; 90% in
Kenya; and 100% in India and the Philippines have been
reported (Alvarez et al. 2005). In Egypt, potato tuber moth
has caused up to 100% losses to potato plants in elds as
well as in storage (Ahmed et al. 2013). Potato tuber moth
is also a pest of tomatoes where larvae damage the leaves,
stems and unripe fruits.
Monitoring
Monitoring of potato tuber moth is a critical part of its
management. Pheromone traps that attract males have been
eective for monitoring potato tuber moth populations.
Monitoring is one of the most important components of an
integrated pest management (IPM) plan for potato tuber
moth. Monitoring gives an indication of insect presence,
population and distribution and allows for timing of
pesticide applications for its management. Pan-water traps
baited with the pheromone can be used for attracting and
monitoring adult male populations. ese traps are easy to
use and clean between readings. Four traps per quadrant of
a circle, about 50  from the periphery of the circle are sug-
gested for monitoring in eld. No economic threshold level
(ETL) has been determined for crop damage or yield loss
in elds. However, checking traps twice a week is suggested
and pesticide application is recommended in case of high
population (e.g., 15 to 20 moths/trap/night) (Anonymous
2013).
Management
e most common method of control of Phthorimaea
operculella is pesticides (Dillard et al. 1993). e develop-
ment of pesticide resistance, resurgence of pest populations
and potential detrimental eects of synthetic pesticides on
non-target organisms has led to the adoption of integrated
pest management (IPM) strategies. It is important to know
the biology and distribution of a pest for an IPM program
to be successful.
Field Management
CULTURAL CONTROL
Weeds and volunteer plants can act as alternate hosts for
potato tuberworms, and should be eliminated from elds
and surrounding areas. Deep planting and good coverage
of potato seeds with soil more than 2 inches during hilling
helps protect damage by adults and larvae. Discard infested
tuber seeds; only use healthy seed tubers for planting. Vines
should not be used for covering tubers as they wilt aer
some time and larvae and moths can penetrate the cover to
reach underlying tubers.
Harvest soon aer crop maturity. Moth populations are
maintained in plant and tuber debris in the eld in the
absence of main crop. erefore, timely eld cleanliness
is an important preventive measure. Cull piles should be
destroyed to reduce overwintering stages of potato tuber-
worm. Avoid leaving harvested tubers overnight in the eld
as these potatoes could act as egg laying sites for potato
tuber moth (Raman 1980, Alvarez et al. 2005, Rondon et al.
2007, Anonymous 2013).
Figure 7. Exposed tubers are predisposed to tuberworm damage.
Credits: Silvia I. Rondon, Hermiston Agricultural Research and
Extension Center, Oregon State University.
Figure 8. Monitoring male adults of the potato tuberworm,
Phthorimaea operculella
(Zeller) on a pheromone-baited trap.
Credits: Silvia I. Rondon, Hermiston Agricultural Research and
Extension Center, Oregon State University.
5
Potato Tuberworm Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae)
SOIL MANAGEMENT AND IRRIGATION
Irrigation is the most eective preventative method under
dry conditions (Raman 1980). Enough irrigation should be
provided to not allow cracks to develop deeper than two
inches in the soil. It is recommended that elds should be
irrigated aer vine desiccation to avoid cracks in the soil
and that harvest of tubers occurs as soon as the skin sets
(Anonymous 2013).
RESISTANT VARIETIES
Host plant resistance enables plants to avoid, tolerate, or
recover from pest infestations (Tingey 1986, Panda and
Khush 1995). e ecacy of other control methods can be
increased using resistant potato cultivars, thus reducing use
of insecticides (Arnone et al. 1998, Golizadeh and Esmaeili
2012). Rondon et al. (2013) studied potato lines at Oregon,
some of which hold promising results for controlling mines
and number of larvae in potato tubers. An earlier study was
conducted at Oregon by Rondon et al. (2009), and it was
conrmed that tubers of the transgenic clone Spunta G2
were resistant to potato tuberworm damage. e resistance
germplasm to potato tuberworm is an important part of an
IPM program for potato tuberworm.
BIOLOGICAL CONTROL
Natural enemies of potato tuber moth can be used as a part
of an IPM program. e parasitoids, Copidosoma koehleri
and Bracon gelechiae Ashmead (Hymenoptera: Braconidae)
have been used with some success in South America and
Australia, respectively (Symington 2003, Alvarez et al.
2005).
BIO-PESTICIDES AND NATURAL CHEMICALS
Bacillus thuringiensis (Bt) formulations have proved eec-
tive for potato tuber moth control in various parts of world
(Alvarez et al. 2005).
In several South American countries, PhopGV-based
biopesticides (Phthorimaea operculella granulovirus (Phop-
GV), genus: Betabaculovirus of the arthropod-infecting
Baculoviridae) are used to control either Phthorimaea
operculella or Tecia solanivora (Zeddam et al. 2013).
CHEMICAL CONTROL
Chemical control might be necessary when adults or larvae
are present. For chemical recommendations for commercial
growers or home gardens, consult your local county Exten-
sion service and be sure to follow all local laws regarding
pesticide use.
Storage Management
Potato tuberworm is a year-long problem under storage
conditions due to continuous breeding of this pest. e
length of life cycle of potato tuberworm is highly dependent
on temperature. So, storage temperature should always be
kept below 52°F. Monitoring in storage situations relies
on the use of pheromone traps. Under storage conditions,
cultural control options involve elimination of damaged
tubers. Screens should be installed at entry points to
exclude moths.
Sanitation of storage facility walls, oors and ceiling is very
important. Treat facility with an approved pesticide, if this
pest was detected the previous year. Use new or thoroughly
sanitized potato sacks, crates, or other containers. Bt spray
can be used on tubers which are mainly used for human
consumption, and pyrethroids on tubers used for seed
purpose (Anonymous 2013).
Selected References
Ahmed AAI, Hashemb MY, Mohamedc SM, Shimaa
Khalila SH. 2013. Protection of potato crop against Ph-
thorimaea operculella (Zeller) infestation using frass extract
of two noctuid insect pests under laboratory and storage
simulation conditions. Archives of Phytopathology and
Plant Protection. DOI:10.1080/03235408.2013.795356.
Alvarez JM, Dotseth E, Nolte P. 2005. Potato tuberworm a
threat for Idaho potatoes. University of Idaho Extension,
Idaho Agricultural Experiment Station, Moscow, ID. (31
Jan 2014)
Anonymous 2013. Potato tuber moth- Tuberworm. Crop-
Watch: Potato Education Guide, UNL Extension. University
of Nebraska-Lincoln, Lincoln, NE. (31 Jan 2014)
Arnone S, Musmeci S, Bacchetta L, Cordischi N, Pucci E,
Cristofaro M, Sonnino A. 1998. Research in Solanum spp.
of sources of resistance to the potato tuber moth, Phthori-
maea operculella (Zeller). Potato Research 41:39-49.
Clough GH, Rondon SI, DeBano SJ, David N, Hamm PB.
2010. Reducing tuber damage by potato tuberworm (Lepi-
doptera: Gelechiidae) with cultural practices and insecti-
cides. Journal of Economic Entomology 103:1306-1311.
Davidson MM, Butler RC, Wratten SD, Conner AJ. 2006.
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maea operculella (Zeller) (Lepidoptera: Gelechiidae). Crop
Protection 25:216-224.
6
Potato Tuberworm Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae)
Dillard HR, Wicks TJ, Philip B. 1993. A grower survey of
diseases, invertebrate pests, and pesticide use on potatoes
grown in South Australia. Australian Journal of Experimen-
tal Agriculture 33:653-661.
Flanders K, Arnone S, Radclie E. 1999. e potato: genetic
resources and insect resistance, pp. 207-239. In: Clement
SL, Quisenberry SS (eds.), Global plant genetic resource for
insect resistant crops. CRC, Boca Raton, FL.
Golizadeh A, Esmaeili N. 2012. Comparative life history
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Golizadeh A, Zalucki MP. 2012. Estimating temperature-
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Malakar R, Tingey WM. 2006. Aspects of tuber resistance
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Panda N, Khush GS. 1995. Host plant resistance to insects.
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mation bulletin 3. International potato center Lima, Peru.
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Schreiber A, Alvarez JM, ornton M, Barbour J, Do-
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of Idaho, Washington State University. (31 Jan 2014)
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tuberworm (Lepidoptera: Gelechiidae). Journal of Eco-
nomic Entomology 102:1649-1653.
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of its biology, ecology, and control. American Journal of
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Author content
... This information is important to understand as we attempt to understand P. operculella migration patterns. Adults can live for 1-2 weeks (Gill et al. 2014), and copulation can take place 16-20 h after adult emergence (Gubbaiah and Thontadarya 1977;Chauhan and Verma 1985;Makee and Saour 2001). Oviposition occurs at night (Attia and Mattar 1939;Broodryk 1970Broodryk , 1971Traynier 1975Traynier , 1983) directed in the foliage or if foliage is not available (Varela and Bernays 1988), directly in tubers (Cannon 1948;Al-Ali et al. 1975;Traynier 1975). ...
... Oviposition occurs at night (Attia and Mattar 1939;Broodryk 1970Broodryk , 1971Traynier 1975Traynier , 1983) directed in the foliage or if foliage is not available (Varela and Bernays 1988), directly in tubers (Cannon 1948;Al-Ali et al. 1975;Traynier 1975). Larvae were described by Moregan and Crumb (1914), Graft (1917), Trivedi and Rajagopal (1992), , Gill et al. (2014), and Rondon and Gao (2018). Sporadically, P. operculella pupae can be found on the surface of tubers; but most of the time they are found in the top 4 cm of the soil (Rondon et al. 2007). ...
... PTM is a widespread and important oligophagous pest of a range of solanaceous species including potato and tomato. It occurs widely in Africa, for example in Ethiopia, Kenya, Egypt gill et al. 2014). The larva feed mainly on potato tubers in both the field and in storage with the most important economic damage in developing countries occurring in storage. ...
... This information is important to understand as we attempt to understand P. operculella migration patterns. Adults can live for 1-2 weeks (Gill et al. 2014), and copulation can take place 16-20 h after adult emergence (Gubbaiah and Thontadarya 1977;Chauhan and Verma 1985;Makee and Saour 2001). Oviposition occurs at night (Attia and Mattar 1939;Broodryk 1970Broodryk , 1971Traynier 1975Traynier , 1983) directed in the foliage or if foliage is not available (Varela and Bernays 1988), directly in tubers (Cannon 1948;Al-Ali et al. 1975;Traynier 1975). ...
... Oviposition occurs at night (Attia and Mattar 1939;Broodryk 1970Broodryk , 1971Traynier 1975Traynier , 1983) directed in the foliage or if foliage is not available (Varela and Bernays 1988), directly in tubers (Cannon 1948;Al-Ali et al. 1975;Traynier 1975). Larvae were described by Moregan and Crumb (1914), Graft (1917), Trivedi and Rajagopal (1992), Rondon (2010), Gill et al. (2014), and Rondon and Gao (2018). Sporadically, P. operculella pupae can be found on the surface of tubers; but most of the time they are found in the top 4 cm of the soil (Rondon et al. 2007). ...
Article
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Arthropods and pathogens constantly challenge potato Solanum tuberosum L. production. Scenarios of climate variation have increased the possibility of changes in pests' biological and ecological patterns by increasing or reducing overwintering length, changes in population growth rates, number of generations, crop-pest relationship, and therefore affecting their expansion. Phthorimaea operculella Zeller (Lepidoptera: Gelechiidae) is one of the main pests affecting potatoes worldwide. Adults oviposit single or multiple eggs in leaves, stems, and tubers, while the larvae in immature stage mine leaves or burrows into tubers turning them unmarketable. Traditional control methods are effective in controlling P. operculella, but many factors determine the success of the control chosen. This review provides key highlights of current information available that could be used as a resource to fight this pest.
... In developing countries, damage to potatoes in storage conditions is the most important economic issue with this pest. 13 In fact, damage during storage can reach 100%, 14 and up to 42% tuber damage was reported in potato storage in Ethiopia. 15 Under field conditions, potato plants can be completely defoliated, resulting in substantial yield losses. ...
... 15 In Egypt, PTM caused up to 100% loss in the field. 13 Furthermore, field infestation is a source of inoculum for damage during storage. 12 Mulatu et al. 17 reported the presence of PTM on tomato in Ethiopia, which caused economic damage to fruits. ...
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BACKGROUND The potato tuber moth (PTM) (Phthorimaea operculella) is a pest of solanaceous species that causes serious damage to potato tubers and tomato fruits. Control is mainly dependent on the use of synthetic chemicals, which pose a risk to the environment and health of farmers, especially in developing countries where application safety rules are often neglected. In this study we aimed at investigating the effects of a plant resistance inducer (PRI) potassium phosphite on PTM larval population density and PTM parasitoid levels, which can be used as biocontrol agents. We also tested whether intercropping with tomato, which is less attractive to PTM, provided a spatial border to further reduce PTM numbers. RESULTS In two different locations over two seasons, we showed that foliar application of phosphite more than halved the PTM larval populations on potato, and that PTM parasitoid numbers were unaffected. No consistent reduction in PTM was achieved by intercropping potato with tomato. CONCLUSIONS Phosphite reduced PTM numbers in the field without interfering with autochthonous parasitoids, indicating its suitability as part of an Integrated Pest Management strategy. Ex situ choice tests showed that phosphite‐treated potato deterred PTM, which could be a reason for the control of PTM in the field. © 2018 Society of Chemical Industry
... The potato tuberworm Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae), also nown as potato tuber moth (PTM), is a major pest of Solanaceae crops globally, and causes widespread economic damage to potatoes, Solanum tuberosum L. (Gill et al., 2014). Potato tuber moth larva feed on leaves and stems, causing serious damage when the insects tunnel into the tubers in the field and during storage (Rondon 2010). ...
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The potato tuber moth (PTM) Phthorimaea operculella (Zeller, 1873) is a major pest of Solanaceae crops globally. PTM is mainly controlled using chemical pesticides. The objectives of this study were to compare the efficacy of two species of entomopathogenic nematode (EPNs), Heterorhabditis bacteriophora Poinar, 1976 and Steinernema feltiae (Filipjev, 1934) Wouts, Mracek, Gerdin & Bedding, 1982, against PTM pre-pupa and pupa, while also assessing their interaction in combination with abamectin in a series of laboratory and greenhouse assays. The results showed that S. feltiae was considerably more virulent than H. bacteriophora against both PTM life stages tested. PTM pupae were less susceptible to EPN than pre-pupae: LC50 values for pupae were 721 and 570 IJs/insect for H. bacteriophora and S. feltiae, respectively; corresponding values for pre-pupae were 98 and 6 IJs/insect, respectively. While both species of EPN were negatively affected by abamectin, the effect on H. bacteriophora was less pronounced. This present study shows that the extent to which the nematodes interact with chemical pesticides is dependent on a number of factors, including nematode species, concentration of combined agents, developmental stage of the targeted pest, exposure method and the complexity of the environment in which the interaction takes place. In the glasshouse study, for S. feltiae, synergistic effects were observed only in the combinations which included lower rates of abamectin and higher S. feltiae concentrations. In the case of H. bacteriophora, other than at the lower concentrations of both the insecticide and the nematode (where the interaction was additive), all other combinations were synergistic. That there were more synergistic interactions in the H. bacteriophora + insecticide combinations is most likely attributable to the lower susceptibility of H. bacteriophora to abamectin compared to S. feltiae. This study demonstrates that combined applications of chemical insecticides and entomopathogenic nematodes allow for a reduction of both inputs. For end users, reducing nematode and abamectin inputs make their combined use an extremely attractive proposition, in both economic terms and as a resistance management strategy.
... The potato tuber moth (PTM), Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae), is a pest of solanaceous crops such as potatoes (Solanum tuberosum L.), tomatoes (Solanum lycopersicum L.) and tobacco (Nicotiana tabacum L.) (Das and Raman, 1994;Gill et al., 2017). It is one of the most important pests causing damage to potato productivity affecting yield and quality of potato crops. ...
Article
The potato tuber moth (PTM)is an oligophagous herbivore and a severe pest of solanaceous crops in many countries of the world. Previously, we reported host expansion and damage potential of PTM on tomato, a congeneric crop of potato. Here we tested adult olfactory behaviour of PTM to leaves of five different cultivated tomato varieties including Moneymaker, Campari, Ailsa craig, LA3475 and E6203, and one wild species, Solanum pimpinellifolium. Tomato leaf hydro-distilled oils of Moneymaker, Campari, Ailsa craig, S. pimpinellifolium and E6203 showed strong attractiveness and LA3475 exhibited repulsiveness for adult PTM of both sexes in two-armed bioassays. Volatiles of Moneymaker, Campari, Ailsa Craig, S. pimpinellifolium and E6203 showed attractiveness for mated adult PTM of both sexes (> 70%). The extracted oil of all tomato leaves contains monoterpenes, sesquiterpenes, diterpenes and C 6 alcohols as well as other components. Phytol is one of the common and major compounds in all tomato varieties. Phytol showed weak attractiveness: 60.8–63.6% and 57.6–60.6% for male and female PTM, respectively when tested at concentrations of 0.1–10 mg/mL. Therefore, the attractiveness of tomato leaf volatiles might be due to synergistic effects of plant volatile mixtures. Identification PTM attractant volatile in tomato leaf is important in its control in environmentally friendly manner.
... Besides field experiments, it is recommended to monitor to the population buildup of PTM in tomato fields. (Das and Raman, 1994;Gill et al., 2017). PTM is considered to be one of the most important constraints to potato productivity affecting yield and quality of the products especially in storage, and increasing the risk of secondary infection of diseases. ...
Thesis
Understanding the host expansion of herbivore insect to other economic crop is vital for agricultural crop protection. Recent climate change and distribution shift of potato tuber moth (PTM), an invaded pest of potato in Korea poses potential threat to congeneric crop of tomato. For this, we approached the risk analysis of the host expansion of PTM into tomato. Risk identification involved entangling the population genetics and dynamics in the field as well as the physisological potential to adapt cold winter. Risk assessment involved evaluating potential threat to tomato from PTM, evaluating development study on tomato leaves and fruits of 6 varieties and also identified possible chemical cue for these interaction. For risk managent, we evaluated convetional insecticide as well as botanical one. We monitored PTM with delta sticky trap and lure impregnated at potato field in Andong area where the highest peak in 2016 was reached on August 11 with average number 19.82 PTM/trap/week whereas at Imha highest peak was on 24th of November and average number of catch was 0.8 PTM/trap/week. The number of PTM catches was lower at potato field but at Imha the PTM catch was increased during 2017 than 2016. Land scape analysis showed that was significant positive correlation between habitat potato field itself and green house with the number of moth catch during the monitoring period. The Super cooling point (SCP) ranges from lowest of ̶ 23.81°C of the egg to highest of ̶ 16.8°C of the fourth instar of larvae (L4). After short period of low temperature acclimation on L3 (Third instar larva), L4 and prepupae, only prepupal stage showed significant lowered SCP from ̶ 20.78 to ̶ 22.37°C. 100% mortality was observed when the larvae or adults were exposed under ̶ 15.1°C environment even in a short period of 2 hr. Results suggest that PTM pupae would be the main overwintering stage in Korea where winter temperature drops down below ̶ 15°C. Since PTM also can inflict damage on other solanaceous crop like tobacco and tomato, we tested the possible host expansion and damage potential on the varieties of tomato. A day old larvae were inoculated to three commercial varieties of tomatoes and a potato. The results showed that PTM could survive and reproduce on tomato leaves or fruits with differential performance on the varieties when compared to potato in choice condition. We tested adult olfactory behavior and larval development on 5 cultivated tomato varieties including Money maker, Campari, Ailsa craig, LA 3475 (M82) and E-6203, and one wild species, S. pimpinellifolium result showed strong attractiveness for mated adult PTM of both sexes (> 70%) in two-armed bioassay. LA 3475 (M82) oil showed repulsive response (83.7% for males and 87.3% for females). GC-MS analysis of the hydro-distilled oils of all tomato leaves contain the fatty acid n-hexadecanoic acid as a major compound with relative percentage as S. pimpinellifollium (32.1%) > E-6203 (26.5%) > money maker (26.1%) > LA-3475 (16.3%) > Campari (15.0%) > Ailsa craig (10.4%). LA 3475 consists of (1-hexyltetraecyl) cyclohexane (10.5%) as the second major compound which was absent in all other tomato varieties. In no choice test, PTM larvae showed highest developmental performances such as number of mines, head capsule size, pupal weight and survival in Ailsa craig, and lowest in LA 3475. The compound contained in S. pimpinellifolium has low level of larval performance. Since from previous chapter we confirmed the there is risk involved that the PTM can be threat to tomato as we observed the PTM in the monitoring in the tomato field and aslo cold hardy and have threat to range and host expansion. So for the risk management we tested the insecticide where, Cartap hydrochloride significantly inhibited the egg hatchability of one (95.75%), two (94%), three (94.24%) and four (89.75%) days old egg. Among the tested insecticide shortest median lethal duration for the field recommended dose was observed for fenthion (LT50, 0.37 hours). LC50 after the 24 hours were found lowest in abamectin (LC50, 0.0052 ppm) followed by emamectin benzoate (LC50, 0.0084 ppm). When tested with Acorus calamus dust in potato tubers similar trend was found in Korean and Nepal origin of sweet flag where mortality significantly changed over times and there was also significant interaction between treatment and times inoculation of neonates) Key word: Phthorimaea operculella, Solanum lycopersicon, Climate change, Pheromones, essential oils, Population structure
... The potato tuber moth (PTM), is a cosmopolitan pest restricted largely to solanaceous crops including potatoes (Solanum tuberosum L.), tomatoes (Solanum lycopersicum L.) and tobacco (Nicotiana tabacum L.) (Das & Raman 1994;Gill et al. 2017). The PTM is considered to be one of the most important constraints to potato productivity affecting yield and quality of the products especially in storage, and increasing the risk of secondary infections and diseases (Foot 1979;Sileshi & Teriessa 2001). ...
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The potato tuber moth (PTM) is an important pest of the potato plant and its tuber. With the expansion of its geographic range, the PTM could be potential threat to the tomato (Solanum lycopersicum L.), a congeneric species of the potato. To assess that risk, we tested larval feeding and development of PTM on leaves of five cultivated tomato varieties namely Moneymaker, Campari, Ailsa Craig, LA3475, E6203 and one wild tomato variety S. pimpinellifolium. PTM larvae accepted all tested plant leaves and developed into adults. Larval development was fastest on the Ailsa Craig variety. Pupae developed fastest on the Moneymaker variety and slowest on LA3475. Host acceptance and survival were highest on Ailsa Craig and lowest on LA3475. The significantly highest male proportion occurred on LA3475 variety. The study showed that PTM could be a potential threat to tomato cultivation which is rapidly increasing in temperate regions owing to climate change.
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Lantana camara, Eucalyptus globulus, Tagetus minuta, Pyrethrum flowers and Azaddiractha indica, were evaluated against potato tuber moth damage with two checks (Diazinon 60% EC and untreated check) at Bako Agricultural Research Center in 2007/2008 and 2008/2009 cropping seasons. A total of 21 huts (cottages) were constructed from locally available materials. Inside each cottage (hut), 1m 2 bed was constructed 65 cm above the ground. Six hundred fifty (650) potato tubers were stored on the bed of each hut in two layers one over the other. The treatments were arranged in a Randomized Complete Block Design (RCBD) with three replications. Plants powder and Diazinon 60% EC were applied respectively, at the rate of 50 gm / bed and 3.5ml / bed at two months’ interval. The treatments that showed promising effects were further advanced on a large bed (2m x3m). Three thousand nine hundred (3900) potato tubers were stored on large beds and 150gm powders were used for each bed. Evaluations were made at the interval of 15 days for 7 consecutive months. Analysis of variance showed that number of potatoes infested and damaged by potato tuber moth was significantly (P0.05) lower in the Lantana camara, Eucalyptus globulus and Pyrethrum flowers than the other treatments, which are similar to standard check. From the study it can be concluded that Lantana camara, E. globulus andPyrethrum flowers can be used to protect seed potatoes from potato tuber moth damage in storage.
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The oviposition deterrent effect of water extract of Spodoptera littoralis and Agrotis ipsilon larval frass on Phthorimaea operculella adult females was studied using two types of larval food “Natural host and Semi-artificial diet” under laboratory and storage simulation (semi-field) conditions. Extracted frass of fed larvae on semi-artificial diet showed complete oviposition deterrent effect at treatments with 4th, 5th and 6th instars of S. littoralis, also at treatments with 1st–3rd and 6th instars of A. ipsilon, while the same effect was observed when the larvae fed on castor oil leaves as a natural host only at treatment with frass extract of A. ipsilon 6th instar larvae. Presence of low amounts of phenols and flavonoids in water extract of A. ipsilon larval frass resulted in relatively more effect as oviposition deterrent to fertile adult females on treated oviposition sites, while the opposite effect was obtained in S. littoralis larval frass experiments. At semi-field experiments, the percentage reduction of laid eggs reached 100% after two days at treatments with frass extracts of 4th and 5th S. littoralis larval instars and A. ipsilon 6th instar larvae fed on semi-artificial diet and/or castor oil leaves. Percentage reduction of laid eggs for untreated sacks reached 93.24 and 48.95% after 2 and 30 days, respectively, when placed between treated sacks, in comparison with the mean number of laid eggs for isolated control.
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The olfactory reaction of larvae and moths was investigated towards 18 oils (6 natural oils and 12 commercial chemical oils). Some of these oils such as peppermint and camphor (natural oils) and eugenol and camphene (commercial oils) were repellent to both larvae and moths. Other oils such as strawberry and d-limonene were attractive to both larvae and moths. Some of the repellent oils were, therefore, tested for their effect on certain biological aspects of the insects. Eugenol and peppermint oils, each at the 0.01% conc., caused a significant depression in the fecundity of moth and decreased the percentage of egg hatchability. Eugenol oil was much more effective than peppermint oil at 1%. Dried (leaves, fruits or seeds) powder of 14 different plants species were tested in different concentrations with talcum powder (carrier material) against egg deposition. The results indicated that dried powders of Allium cepa, Curcuma longa, Colocasia antiqurum, Ocimum basilicum. Dodonaea viscose and Thuja orientalis played a highly significant role in reducing egg deposition. The most impressive effect was displayed by powders of D. viscose and A. cepa, which caused the highest depression in egg deposition as well as in the emerging offsprings. Ethanolic extracts of 11 plants indicated that extracts of Pithuranthos tortosus and Iphiona scabra caused the maximum inhibition of egg hatchability, followed by C. longa, Citrullus colocynthia and T. orientalis. Ethanolic extracts of Schinus terebenthiflius (leaves) and I. scabra caused the highest depression in the deposited eggs, as they played a remarkable role as ovipositor deterrents. The majority of the plant extracts at 1% conc. could protect potato tubers at different intervals according to the calculated tuber damage index as follows: Iphiopna > Pithuranthos > Curcuma > Schinus (fruits) Thuja > Schinus (leaves) > Dodonaea > Citrullus.
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Chapter
The development and deployment of crop varieties defended or tolerant against insect attack is a major tactic in pest management. In agricultural terms, plant resistance to insects is a property that enables a plant to avoid, tolerate, or recover from the injurious effects of insect feeding and oviposition. Plants vary considerably in their mechanisms for defense against insects. Defensive strategies range from disruption of insect behavior and development to repair or replacement of organs and tissues damaged through insect attack. The purpose of this chapter is to present research methods and considerations appropriate for: (1) evaluation and development of insect-resistant cultivars, and (2) analysis of plant traits conferring resistance. Additional information of this type is provided by Chesnokov (1962), Dahms (1972), Smith (1978), Tingey and Pillemer (1977), and Maxwell and Jennings (1980).
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The potato tuberworm, Phthorimaea operculella (Zeller) (PTW), is one of the most important limitations to potato, Solanum tuberosum L., productivity worldwide. Leaves, stems, petioles and more importantly, potato tubers, in the field and storage can be seriously affected. Due to the relatively recent arrival of the PTW in the United States Pacific Northwest, the local and regional lines have never been screened for tuber resistance to PTW. Thus, the objective of this study was to screen regional potato lines for potential PTW resistance by tubers under field and laboratory conditions. Experiments were conducted at the Hermiston Agricultural Research and Extension Center in Hermiston Oregon in 2006 and 2007. Accessions that had few number of mines per tuber were AC97521-1R/Y, Q174-2, Rubi, Yuguima, Paciencia, TM-3, KWPTM24 and CIP 780660; lines than had few larvae per tuber were A97287-6, PA00N10-5, AC97521-1R/Y, Q174-2, PA04LNC2-1, PA04LNC4-1, TM-3 and CIP 780660. Incorporating host plant resistance to tuber penetration by PTW larvae together with appropriate cultural practices including limitation of exposure time of tubers in the field and judicious use of chemicals may provide the best sustainable management option.
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Among the major insect pests of potato, the potato tuber moth Phthorimaea operculella (Zeller) is important in both field and storage. The biology of the pest, studies of spatial distribution, sampling technique, effect of density dependent and Independent factors, losses caused and economic threshold levels are reviewed. Various management strategies such as agronomic practices, biological and chemical control are discussed. Attempts to identify the potential components of management of potato tuber moth are made.
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In 1991, a survey was distributed to 251 potato growers in South Australia to determine major diseases, insect and other invertebrate pests, and chemicals used to control them. The overall response rate was 48%, but of these, 24 individuals were no longer growing potatoes. The results were summarised for the State and by district (Adelaide Hills, Adelaide Plains, Murray Lands, South East). The most prevalent diseases encountered by respondents in all districts were target spot caused by Alternaria solani, and rhizoctonia canker caused by Rhizoctonia solani. Other diseases of concern to growers included late blight caused by Phytophthora infestans, seed piece decay caused by various pathogenic and saprophytic microorganisms, common scab caused by Streptomyces scabies, and leaf roll caused by potato leaf roll virus. The most commonly used fungicides for disease control were chlorothalonil (33-42% of respondents), mancozeb (30%), and cupric hydroxide (11-13%). The most commonly used seed treatments for control of seed piece decay were mancozeb (51 % of respondents), tolclofos methyl (24%), and lime (20%). Green peach aphid (Myzus persicae), potato aphid (Macrosiphum euphorbiae), potato moth (Phthorimaea operculella), and jassids and leafhoppers (Jassidae, Cicadellidae) were the pests of greatest concern to the growers. Others included Rutherglen bug (Nysius vinitor), redlegged earth mite (Halotydeus destructor), and thrips (Thripidae). The most commonly used insecticides were ethamidophos (40% of respondents), monocrotophos (22-28%), and dimethoate (7-13%).