Frontiers, Oviposition Preference of Pea Weevil, Bruchus pisorum L
Frontiers in Plant Science
- 1 Frontiers in Plant Science
- 2 Plant Breeding
- 3 Original Research ARTICLE
- 4 Oviposition Preference of Pea Weevil, Bruchus pisorum L. Among Host and Non-host Plants and its Implication for Pest Management
- 5 Introduction
- 6 Materials and Methods
- 7 Results
- 8 What Are Pea Weevils: Information For Control Of Pea Weevil Pests
- 9 What are Pea Weevils?
- 10 Control of Pea Weevil
- 11 Bruchus pisorum (pea weevil)
Maria Carlota Vaz Patto
Institute of Chemical and Biological Technology, New University of Lisbon, Portugal
Norwegian Institute for Agricultural and Environmental Research, Norway
Isabel R. Teixeira
IFSULDEMINAS — campus Poços de Caldas
The editor and reviewers’ affiliations are the latest provided on their Loop research profiles and may not reflect their situation at the time of review.
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Original Research ARTICLE
Oviposition Preference of Pea Weevil, Bruchus pisorum L. Among Host and Non-host Plants and its Implication for Pest Management
- 1 Department of Plant Protection Biology, Swedish University of Agricultural Sciences, Alnarp, Sweden
- 2 International Institute of Tropical Agriculture, Ibadan, Nigeria
The pea weevil, Bruchus pisorum L. is a major insect pest of field pea, Pisum sativum L. worldwide and current control practices mainly depend on the use of chemical insecticides that can cause adverse effects on environment and human health. Insecticides are also unaffordable by many small-scale farmers in developing countries, which highlights the need for investigating plant resistance traits and to develop alternative pest management strategies. The aim of this study was to determine oviposition preference of pea weevil among P. sativum genotypes with different level of resistance (Adet, 32410-1 and 235899-1) and the non-host leguminous plants wild pea (Pisum fulvum Sibth. et Sm.) and grass pea (Lathyrus sativus L.), in no-choice and dual-choice tests. Pod thickness and micromorphological traits of the pods were also examined. In the no-choice tests significantly more eggs were laid on the susceptible genotype Adet than on the other genotypes. Very few eggs were laid on P. fulvum and L. sativus. In the dual-choice experiments Adet was preferred by the females for oviposition. Furthermore, combinations of Adet with either 235899-1 or non-host plants significantly reduced the total number of eggs laid by the weevil in the dual-choice tests. Female pea weevils were also found to discriminate between host and non-host plants during oviposition. The neoplasm (Np) formation on 235899-1 pods was negatively correlated with oviposition by pea weevil. Pod wall thickness and trichomes might have influenced oviposition preference of the weevils. These results on oviposition behavior of the weevils can be used in developing alternative pest management strategies such as trap cropping using highly attractive genotype and intercropping with the non-host plants.
Field pea, Pisum sativum L. is a cool season legume crop grown in tropical highlands and in many countries in temperate regions (Messiaen et al., 2006). It is an important crop both for human consumption and for animal feed mainly due to its high protein content, and thus nutritional value. Furthermore, it provides ecosystem services by improving soil fertility through symbiotic nitrogen fixation (French, 2004; Khan and Croser, 2004; Messiaen et al., 2006). Insect pests are one of the major constraints of field pea production (Clement et al., 2000), among which the pea weevil, Bruchus pisorum L. is an economically important pest of field pea worldwide. In Ethiopia, seed damage and weight loss up to 85 and 59%, respectively, has been reported after attack by the pea weevil (Teka, 2002; Seyoum et al., 2012). As a consequence, the damaged seeds have low marketable value, are less valuable for human consumption and animal feed and show poor germination rate (Brindley et al., 1956; Clement et al., 2000, 2002; Seyoum et al., 2012).
The pea weevil has one generation per year and it reproduces only on field pea. Upon emergence from hibernation sites adult weevils fly into the pea fields and start to search for mate and oviposition sites. Egg laying starts about 2–2.5 weeks after the arrival of the weevils. The female weevil lays its eggs on pods of peas and upon hatching the first instar larva bore directly to the seed. Larvae develop inside the seed by consuming the content of the seed, which results in damage to the crop (Brindley et al., 1956). This cryptic larval feeding habit within the seeds makes it difficult both to monitor the infestation and to control the pea weevil with chemical insecticides. Thus, the most suitable time to control the pest would be before females commence oviposition (Horne and Bailey, 1991; Baker, 1998; Clement et al., 2000). Due to the long infestation period of adult weevils it has been reported that repeated chemical spraying is required to be effective (Baker, 1998). Furthermore, fumigation of harvested peas in the store can prevent further damage by pea weevil (Baker, 1998; Clement et al., 2000). However, insecticides are often unaffordable for small-scale farmers in developing countries such as in Ethiopia. Furthermore, insecticides can have adverse effects on human health and the environment. For example, recent studies showed improper use of insecticides among field pea growers in Ethiopia can expose the farmers to pesticide risks (Mendesil et al., 2016). Thus, development of alternative pest management strategies is needed.
Understanding of oviposition preference behavior in relation to host and non-host plants may provide useful information for developing alternative pest management strategies such as intercropping and trap cropping strategy for insect pest management (Shelton and Badenes-Perez, 2006; Cook et al., 2007; Finch and Collier, 2012). Intercropping is a traditional agronomic practice in Africa which has been shown to reduce pest damage (Abate et al., 2000; Smith and McSorley, 2000) and increase productivity of farm land (Vandermeer, 1989). A study conducted in Ethiopia showed that intercropping of maize, Zea mays L. with Ethiopian mustard, Brassica carinata A. Braun and potato, Solanum tuberosum L. reduced infestation by the stem borers, Busseola fusca Füller and Chilo partellus (Swinhoe) (Wale et al., 2007). A plant species or variety which is attractive to insect pest can also be planted as a trap crop to protect the main crop (Shelton and Nault, 2004; Shelton and Badenes-Perez, 2006). Trap cropping has been developed for control of various insect pests (a review of Shelton and Badenes-Perez, 2006) and there is an increasing interest in the use of trap crops for pest management.
In many herbivorous insects, understanding female choice of oviposition site is important for evaluating plant resistance and interaction between plants. Among a variety of plants, insect herbivores often show higher preference for particular host plant species, crop varieties and/or crop stages for feeding and oviposition (Bernays and Chapman, 1994). Thus, there can be large differences in plant attractiveness and resistance between different host plants and varieties of the same crop (Smith, 2005). Furthermore, various studies have shown that non-host plants can influence insect herbivore behavior in different ways such as disturbing host finding, masking of host plants and as an oviposition repellent (Vandermeer, 1989; Finch and Collier, 2012; Ratnadass et al., 2012). Most insect herbivores rely on morphological and chemical cues in location of oviposition sites and both morphological traits and secondary chemical metabolites play a crucial role in plant resistance against insect pest attack (Bernays and Chapman, 1994). Plant traits such as different types of glandular structures, wax layers and tissue thickness have been shown to influence oviposition behavior of insect herbivores (Bernays and Chapman, 1994).
In previous field experiments, we found variation in the susceptibility to pea weevil attack between different field pea genotypes, of which Adet genotype is highly susceptible to the weevil, and 235899-1 and 32410-1 are moderately resistant based on mean percent seed damage (Teshome et al., 2015). There are also studies showing that non-host plants also can affect host plant choice behaviors of the pea weevil (Annis and O’Keeffe, 1984b). Furthermore, a specific morphological trait reported in peas is the growth of neoplasm on the pod surface, a ‘postular-like outgrowth’ that is controlled by a single dominant gene, Np (Nuttall and Lyall, 1964). Oviposition of pea weevil on peas with Np gene has been found to result in development of neoplasm (Berdnikov et al., 1992; Doss et al., 2000). Interestingly, neoplasms are also formed when peas with Np gene are grown in the greenhouse under reduced UV wavelengths (Nuttall and Lyall, 1964; Snoad and Matthews, 1969). However, there is little information about how oviposition behavior in the pea weevil reflects resistance among genotypes and how it is affected by non-host plants. There is also no information if it is possible to take advantage of neoplasm as a resistant trait against pea weevil.
Although intercropping and trap cropping pest management methods have been used for major insect pests in various cropping systems elsewhere, e.g., control of B. fusca and C. partellus in maize and sorghum, Sorghum bicolor (L.) Moench in Africa (Khan et al., 2014), there is no available information on such management methods for pea weevil. Identifying host plants that are preferred to female pea weevil and those that are less or non-preferred, may pave the way to develop intercropping and trap cropping as pest management strategies for the pea weevil. Therefore, the aim of this study was to determine oviposition preference of pea weevil to field pea genotypes with different level of pea weevil resistance and to non-host plants. We also wanted to determine the influence of pod morphological traits and neoplasm formation on oviposition preference by pea weevil.
Materials and Methods
Three field pea, P. sativum L., genotypes were selected based on results obtained from field experiments conducted in northern and north-western Ethiopia during 2011–2012: Ebinat (12°10′ N 38° 05′ E), Liben (11° 50′N 37°10′ E), and Sekota (13° 00′ N 38° 50′E) (Teshome et al., 2015). The genotypes were: Adet, an improved variety which is highly susceptible to pea weevil, released by Adet Agricultural Research Center in Ethiopia in 1997, and 235899-1 and 32410-1 that both are gene bank accessions that were found moderately resistant (Teshome et al., 2015) obtained from the Ethiopian Institute of Biodiversity in Addis Ababa, Ethiopia. Furthermore, 235899-1 is a Np genotype with neoplasm formation in pods. Two non-host plants to pea weevil, wild pea, Pisum fulvum Sibth. et Sm. (NGB 102148) and grass pea, Lathyrus sativus L., were also included in the experiment. P. fulvum was obtained from the Nordic Genetic Resource Center (NordGen), Alnarp, Sweden whereas L. sativus was collected from Adet area, Ethiopia. Plants were grown to produce flowering branches and pods for the insect studies. All plants were grown in 2-L plastic pots with humus rich gardening soil (Weibulls, Sweden) in a biotron chamber (22°C, 75% RH, 12:12 h light/dark cycle) in 2014 at SLU, Alnarp.
Field pea seeds infested with B. pisorum were obtained from harvest of field experiments conducted in Liben, north-western Ethiopia during 2011–2012 and from farmers’ seed stores in this area. Infested seeds were kept in a transparent plastic insect rearing cage (31 cm × 22.5 cm × 12 cm) at room temperature (20–24°C). Newly emerged adult pea weevils were used for the bioassays. The sex of the weevils was determined based on the presence of a small spine on the tibia of the middle leg of only male insects (Bousquet, 1990). Newly emerged weevils can be kept alive up to 1 year.
A no-choice oviposition assay was conducted following the methods of Hardie and Clement (2001) and Clement et al. (2002) with some modification. A pair of male and female B. pisorum was introduced into a plastic insect rearing cage (31 cm × 22.5 cm × 12 cm) that was placed in a climate chamber (24°C, 60% RH, 12:12 h light/dark cycle). The weevils were provided a branch of a field pea plant with four to six fresh flowers every 2 days for 10 days before each experiment. In addition, weevils were provided distilled water and sugar solution on a cotton swab, which was changed every week. At the start of the experiment two flat pea pods, which is the preferred stages for oviposition by pea weevil (Hardie and Clement, 2001), were provided for oviposition. Each pod was placed hanging from the top of the cage using paper clip without damaging the pod, then a staples magnet (10 mm, Staples, Inc. Amsterdam, The Netherlands) was placed on the outer surface of the cage in order to fix/attach the pod. Only pods of one genotype per cage (Adet, 235899-1, 32410-1, P. fulvum and L. sativus) were provided to each weevil. Pods were changed daily and the number of eggs laid on each pod was counted under stereo microscope. For each experimental setup ten replications were made in a completely randomized design. The weevils were allowed to oviposit for 10 days.
A similar experimental procedure as described above was followed in the dual-choice experiments, except that one pod of the control (Adet) and one pod from four test genotypes (235899-1, 32410-1, P. fulvum and L. sativus) were placed in each cage.
Degree of Neoplasm Formation on Pods of 235899-1
In order to determine the association of degree of neoplasm formation and number of eggs laid by the weevil, pods of 235899-1, which were selected for no-choice oviposition bioassay were first assessed for degree of neoplasm before oviposition assays. The degree of neoplasm formation was determined into four classes (1–4; Figure 3A), where 1 = 75% of the pod surface is covered with neoplasm. Then the level of neoplasm formation was correlated with (related to) the number of eggs laid per pod. Twenty pods were sampled for each class and in total eighty pods were sampled for this study.
Morphological Traits of Test Genotypes
Thickness of pod wall was measured using an Absolute Digimatic Caliper (500-182-30, Mitutoyo, Japan). A measurement was done in the middle of both on the upper and bottom part of the pod. In total forty pods were measured per each test genotype (Adet, 235899-1, 32410-1, P. fulvum and L. sativus), where four fresh pods of flat stage were sampled from ten different plants.
Scanning Electron Microscopy
Scanning electron microscopy (SEM) was performed at SLU, Alnarp to examine if there were any differences on the pod anatomy of test genotypes. Fresh pods of flat stage were sampled from Adet, 32410-1, 235899-1, P. fulvum and L. sativus. Small pieces of the pods were fixed overnight at 4°C in a solution of 2.5% glutaraldehyde and 2% paraformaldehyde in 0,1 M Na-phosphate buffer, pH 7.2, dehydrated in a graded series of ethanol and critical-point dried (CPD 020, Balzers, Lichtenstein). Sample pieces were attached on stubs with double-sided tape external, internal or cros section surface of the pod upwards, and coated with a mixture of gold and palladium 3:2 in a sputter (JFC-1100, JOEL, Tokyo, Japan). Coated samples were examined with SEM (435VP, LEO Electron Microscopy Ltd., Cambridge, UK) with 10 kV.
No-choice oviposition and genotype combination data, and pod wall thickness was analyzed using one-way analysis of variance (ANOVA) using a generalized linear model. Mean oviposition were logarithmic transformed before analysis. For dual-choice test a Student’s t-test was used to analyze differences in oviposition on control vs. test genotypes. Spearman’s correlation analysis was used to determine the associations of number of eggs laid and level of neoplastic formation. All statistical analysis was done using MINITAB 16 statistical software.
Oviposition Preference Test
There were clear differences in the number of eggs laid on the different genotypes (F = 121.53; df = 4; P ∗∗ P 51% neoplasm formation (Figures 3A,B). We found a negative correlation between the degree of neoplasm formation and number of eggs laid per pod (rs = -1.0; P Keywords : Bruchidae, host selection, insect behavior, legume, neoplasm, Pisum sativum, pea weevil
Citation: Mendesil E, Rämert B, Marttila S, Hillbur Y and Anderson P (2016) Oviposition Preference of Pea Weevil, Bruchus pisorum L. Among Host and Non-host Plants and its Implication for Pest Management. Front. Plant Sci. 6:1186. doi: 10.3389/fpls.2015.01186
Received: 12 August 2015; Accepted: 10 December 2015;
Published: 06 January 2016.
Maria Carlota Vaz Patto, Instituto de Tecnologia Quimica e Biologica/Universidade Nova de Lisboa, Portugal
Anne-Kristin Løes, Bioforsk Norwegian Institute of Agricultural and Environmental Research, Norway
Isabel Ribeiro Do Valle Teixeira, IFSULDEMINAS – Campus Poços de Caldas, Brazil
Copyright © 2016 Mendesil, Rämert, Marttila, Hillbur and Anderson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
What Are Pea Weevils: Information For Control Of Pea Weevil Pests
Does something seem amiss with your pea crop? Perhaps you have noticed insects feeding on the blossoms or tiny eggs on the pea pods. If so, the culprits are very likely pea weevil pests. Pea weevil damage is a major menace to pea production, specifically to garden and canning peas. What are pea weevils, anyway? Keep reading to find out.
What are Pea Weevils?
Pea weevil pests are small, black to brownish insects with a white zigzag running across the back. Bruchus pisorum overwinter in plant debris in the soil and then lay their eggs on the pea pods. Pea weevil larvae hatch and burrow into the pods and feed on the developing peas while adults munch on the blossoms.
The resulting pea weevil damage on the pea crop renders it unfit for sale in the commercial sector and unappetizing for the home gardener. Not only does this pea weevil infestation affect the germination potential of developing peas, but in the commercial arena, costs many dollars separating and discarding infested pea pods.
Control of Pea Weevil
The control of pea weevil pest is of paramount importance in relation to the commercial pea crop industry and it may be of a high importance to the home gardener as well.
Controlling pea weevils in the pea farm may be attained with the use of a dust mixture containing ¾ of 1 percent of rotenone. One to three dustings may be necessary to gain the upper hand on the pea weevil infestation at just the correct life cycle of the pea. The primary dusting should occur when the peas first begin to bloom, but before pods have set.
Successive application should occur depending upon weevil migrations that may afflict the field after the first rotenone application. This same dusting procedure will work in the home garden with a hand duster and should be repeated at weekly intervals throughout the growing season.
For the home gardener, however, the first order of business when controlling pea weevil infestations is to clean and dispose of any debris in the garden where the pests can potentially overwinter. Spent vines should be pulled and destroyed immediately post-harvest. The pulling of the vines before the peas are dry is the wisest course of action, although piling and burning will work just as well.
Any that are left in the garden should be plowed underground 6-8 inches. This practice will prevent any eggs deposited from hatching or developing and infesting the pea crop the following year.
Bruchus pisorum (pea weevil)
- Last modified
- 21 November 2019
- Datasheet Type(s)
- Preferred Scientific Name
- Bruchus pisorum
- Preferred Common Name
- pea weevil
- Taxonomic Tree
- Domain: Eukaryota
- Kingdom: Metazoa
- Phylum: Arthropoda
- Subphylum: Uniramia
- Class: Insecta
- Summary of Invasiveness
- The pea weevil is a small insect (up to 5 mm long) with good flight possibilities. The adults may fly up to 5 km in search of pea flowers. The larvae develop within a single pea seed; the pupae and newly emerged adults also remain there, so the pest.
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Picture Title Caption Copyright Title Ova Caption Bruchus pisorum (pea weevil); eggs (arrowed) are yellow, cigar-shaped and measure 1.5 x 0.6mm. They are laid singly or in pairs, and attached to green pods. Copyright ©Radoslav Andreev & I. Manolov/Agricultural University, Plovdiv, Bulgaria Ova Bruchus pisorum (pea weevil); eggs (arrowed) are yellow, cigar-shaped and measure 1.5 x 0.6mm. They are laid singly or in pairs, and attached to green pods. ©Radoslav Andreev & I. Manolov/Agricultural University, Plovdiv, Bulgaria Title Adult female Caption Bruchus pisorum (pea weevil); the females lay eggs on developing (immature) pea pods. Oviposition starts 5-52 hours after mating. Copyright ©Radoslav Andreev & I. Manolov/Agricultural University, Plovdiv, Bulgaria Adult female Bruchus pisorum (pea weevil); the females lay eggs on developing (immature) pea pods. Oviposition starts 5-52 hours after mating. ©Radoslav Andreev & I. Manolov/Agricultural University, Plovdiv, Bulgaria Title Adult Caption Bruchus pisorum (pea weevil); adults are ovoid, chunky beetles, ca.5.0mm in length. They are brownish, flecked with white, black and grey patches, and covered with short hairs or scales. The tip of the abdomen is exposed behind the wing covers and is white marked with two black oval spots. There is a visible white ‘cross’ mark. Copyright ©Radoslav Andreev & I. Manolov/Agricultural University, Plovdiv, Bulgaria Adult Bruchus pisorum (pea weevil); adults are ovoid, chunky beetles, ca.5.0mm in length. They are brownish, flecked with white, black and grey patches, and covered with short hairs or scales. The tip of the abdomen is exposed behind the wing covers and is white marked with two black oval spots. There is a visible white ‘cross’ mark. ©Radoslav Andreev & I. Manolov/Agricultural University, Plovdiv, Bulgaria Title Damage symptoms Caption Bruchus pisorum (pea weevil); damaged dry pea seeds. An opaque circular ‘window’ is visible (arrowed) on the pea. The fully-grown larva prepares an exit hole and pupates behind this ‘window’. Due to cannibalism, only one larva completes its development. The new generation of adult beetles pushes the window open and leaves the seed, creating a 5mm exit hole. Copyright ©Radoslav Andreev & I. Manolov/Agricultural University, Plovdiv, Bulgaria Damage symptoms Bruchus pisorum (pea weevil); damaged dry pea seeds. An opaque circular ‘window’ is visible (arrowed) on the pea. The fully-grown larva prepares an exit hole and pupates behind this ‘window’. Due to cannibalism, only one larva completes its development. The new generation of adult beetles pushes the window open and leaves the seed, creating a 5mm exit hole. ©Radoslav Andreev & I. Manolov/Agricultural University, Plovdiv, Bulgaria
Preferred Scientific Name
- Bruchus pisorum Linnaeus, 1758
Preferred Common Name
Other Scientific Names
- Bruchus cruciger Geoff.
- Bruchus pisi Linnaeus
- Bruchus salicis Skop.
- Callosobruchus pisorum Linnaeus
- Dermestes pisorum Linnaeus, 1758
- Laria pisorum Linnaeus
- Mylabris pisorum Linnaeus
International Common Names
- English: beetle, pea; pea beetle; pea seed beetle; weevil, pea
- Spanish: brucho del poroto; bruco de la arveja; bruquido de las arvejas; brúquido de las arvejas; gorgojo de la arveja; gorgojo de la arveja y garbanzos; gorgojo de los chicharos; gorgojo del frijol y arveja; picudo del guisante
- French: bruche du pois; bruchide des poix
- Portuguese: caruncho da ervilha; gorgulho da ervilla
Local Common Names
- Austria: Erbsenkafer
- Belgium: erwtekever
- Bulgaria: grahov zarnoyad
- Croatia: graskov zizak
- Czech Republic: zrnokaz hrachov; zrnokaz hrachový; zrnokaza hrachového
- Denmark: Ærtefrøbille
- Ethiopia: yeater nekez
- Finland: hernepiilokas
- Germany: Gemeiner Erbsen Kaefer; Grosser Erbsen Kaefer; Kaefer, Gemeiner Erbsen-; Kaefer, Grosser Erbsen-
- Hungary: borsózsizsik
- Israel: zaryit haafuna
- Italy: bruco del pisello; pappice; tonchio del pisello
- Japan: endo-zomusi
- Latvia: zirnu seklgrauzis
- Netherlands: erwte kever
- Norway: ertefrobille
- Poland: strakowca grochowego
- Romania: gargaritei
- Slovenia: ggraharja
- Sweden: ärtsmyg
- Turkey: bezelye böcegi; bezelye tohumböcegi
- Ukraine: zernivka gorohova
- Yugoslavia (Serbia and Montenegro): graskovog zizka
- BRCHPI (Bruchus pisorum)
Summary of Invasiveness
The distribution in this summary table is based on all the information available. When several references are cited, they may give conflicting information on the status. Further details may be available for individual references in the Distribution Table Details section which can be selected by going to Generate Report.
Last updated: 10 Jan 2020
Continent/Country/Region Distribution Last Reported Origin First Reported Invasive Reference Notes
Ethiopia Present, Widespread CABI (Undated) Original citation: Assefa and et al. (2003) Nigeria Present CABI (Undated) Original citation: Olaifa (2000) Bangladesh Present, Widespread APPPC (1987); CABI (Undated) China Present APPPC (1987) Hong Kong Present CABI (Undated) Original citation: Hong Kong Government Information Centre, 2003 India Present, Widespread CABI (Undated) Original citation: Raina (1971) -Jammu and Kashmir Present, Widespread CABI (Undated) Original citation: Bhat (1988) -Manipur Present, Widespread CABI (Undated) Original citation: Barwal and Devi (1993) -Punjab Present, Widespread CABI (Undated) Original citation: Pajni and Sood (1975) Iran Present CABI (Undated) Original citation: Abivardi (1976) Iraq Present, Widespread CABI (Undated) Original citation: Al-Rawy and Kaddou (1971) Japan Present, Few occurrences Lincoln Plant Protection Centre (1985); Lund University (2003) Kazakhstan Present, Widespread CABI (Undated) Original citation: Aleksandrova (1977) Nepal Present, Widespread CABI (Undated) Original citation: Pandey et al. (2000) South Korea Present KSAE (1989); CABI (Undated) Syria Present, Widespread CABI (Undated) Original citation: Weigand and et al. (1994) Tajikistan Present CABI (Undated) Original citation: Kadamshoev (1985) Turkey Present CABI (Undated) Original citation: Kalkan (1972)
Albania Present BBA (2003) Austria Present CABI (Undated) Original citation: Weinhappel and et al. (1996) Belgium Present CABI (Undated) Original citation: Rombaut (2003) Bulgaria Present, Widespread CABI (Undated) Original citation: Lazarov (1931) Cyprus Present Lund University (2003) Czechia Present AGRITEC (2003) Denmark Present CABI (Undated) Original citation: Hansen and et al. (1991) Estonia Present CABI (Undated) Original citation: Remm (1967) France Present, Widespread CABI (Undated) Original citation: Eschenbrenner and Taupin (1983) Germany Present CABI (Undated) Original citation: El Titi (1980) Greece Present Lund University (2003) Hungary Present CABI (Undated) Original citation: Jermy and Szentesi (1978) Italy Present, Widespread CABI (Undated) Original citation: Parisi and Govoni (1998) Latvia Present CABI (Undated) Original citation: Telnov and et al. (2003) Moldova Present, Widespread CABI (Undated) Original citation: Sokolov, 1977 Poland Present, Widespread CABI (Undated) Original citation: Wnuk and Wiech (1987) Portugal Present Mateus et al. (2003) Romania Present, Widespread CABI (Undated) Original citation: Boguleanu and et al. (1969) Russia Present CABI (Undated a) Present based on regional distribution. -Central Russia Present, Widespread Volkov et al. (1955) -Northern Russia Present Volkov et al. (1955) -Southern Russia Present, Widespread Volkov et al. (1955) -Western Siberia Present CABI (Undated) Original citation: Legalov (2003) Serbia Present, Widespread CABI (Undated) Original citation: Almasi (1990) Slovakia Present CABI (Undated) Original citation: Cejka (2003) Slovenia Present Agroruse (2003) Spain Present, Widespread CABI (Undated) Original citation: Marzo and et al. (1997) Sweden Present Lund University (2003) Ukraine Present, Widespread CABI (Undated) Original citation: Sanin and et al. (1975) United Kingdom Present MapMate (2003)
Canada Present CFIA (2003) United States Present CABI (Undated a) Present based on regional distribution. -Idaho Present, Widespread CABI (Undated) Original citation: Pesho and et al. (1977) -Kansas Present Introduced Kansas Pest Code List (2003) -Montana Present CABI (Undated) Original citation: Montana and Department of Agriculture (2003) -Oregon Present Introduced Invasive CABI (Undated) Original citation: Systma and et al. (2003) -Washington Present, Widespread CABI (Undated) Original citation: Pesho and et al. (1977) -Wisconsin Present CABI (Undated) Original citation: University of Wisconsin Madison, 2003
Australia Present CABI (Undated a) Present based on regional distribution. -New South Wales Present, Widespread Introduced CABI (Undated) Original citation: Goodyer (1987) -South Australia Present, Widespread Introduced CABI (Undated) Original citation: Nourse (1973) -Victoria Present, Widespread Introduced CABI (Undated) Original citation: Comery and (1984) -Western Australia Present, Widespread Introduced CSIRO/AFFA (2003) New Zealand Present Lincoln Plant Protection Centre (1985)
Argentina Present, Widespread CABI (Undated) Original citation: Via rural (2003) Chile Present, Widespread CABI (Undated) Original citation: Cafati and Jimenez (1974) Peru Present, Widespread ALNICOLSA (2003)
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Category Sub-Category Habitat Presence Status Terrestrial
List of Symptoms/Signs
Sign Life Stages Type Seeds / internal feeding
Natural enemy Type Life stages Specificity References Biological control in Biological control on Dinarmus basalis Parasite Larvae Paecilomyces fumosoroseus Pathogen Larvae Strongygaster triangulifera Parasite Adults Triaspis thoracicus Parasite Larvae Australia; Canada peas Trichomalopsis leguminis Parasite Larvae Uscana chiliensis Parasite Eggs Uscana senex Parasite Eggs Republic of Georgian; Ukraine peas
Plant parts liable to carry the pest in trade/transport Pest stages Borne internally Borne externally Visibility of pest or symptoms True seeds (inc. grain) adults; larvae; pupae Yes Pest or symptoms usually invisible Plant parts not known to carry the pest in trade/transport Bark Bulbs/Tubers/Corms/Rhizomes Flowers/Inflorescences/Cones/Calyx Fruits (inc. pods) Growing medium accompanying plants Leaves Roots Seedlings/Micropropagated plants Stems (above ground)/Shoots/Trunks/Branches Wood
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