| Legend |
|---|
| Justification for qualification based on EPPO PM 4 Standards |
| Justification for disqualification |
| Additional or non-conclusive information |
| Standard text |
NAME OF THE ORGANISM: Resseliella theobaldi (THOMTE)
GENERAL INFORMATION ON THE PEST
Name as submitted in the project specification (if different):
Pest category:
Insecta
1- Identity of the pest/Level of taxonomic listing:
Is the organism clearly a single taxonomic entity and can it be adequately distinguished from other entities of the same rank?
Yes
Is the pest defined at the species level or lower?:
Yes
Can listing of the pest at a taxonomic level higher than species be supported by scientific reasons or can species be identified within the taxonomic rank which are the (main) pests of concern?
- Not relevant: Fruits (including hops) sector
If necessary, please list the species:
-
Is it justified that the pest is listed at a taxonomic rank below species level?
Not relevant
Conclusion:
- Null: Fruits (including hops) sector
Justification (if necessary):
-
2 – Status in the EU:
Is this pest already a quarantine pest for the whole EU?
No
Presence in the EU:
Yes
List of countries (EPPO Global Database):
-
Conclusion:
Candidate
Justification (if necessary):
Resseliella theobaldi) is widespread in Europe on raspberries, both in field grown crops and under protected cultivation (Gordon et al., 2002; Vetek et al., 2006b).
HOST PLANT N°1: Rubus idaeus {Rubus} (RUBID) for the Fruits (including hops) sector.
Origin of the listing:
Commission Implementing Directive (EU) 2014/98/EU and Commission Implementing Regulation (EU) 2019/2072
Plants for planting:
Plants intended for planting
3 - Is the pest already listed in a PM4 standard on the concerned host plant?
Yes
Conclusion:
Evaluation continues
Justification (if necessary):
EPPO Standard PM 4-10 Certification scheme for Rubus recommends inspection for Resseliella theobaldi as appropriate to the Rubus sp. or hybrid concerned. However, in the responses to the questionnaire, ES and SI supported deregulation in the EU; considering that plants for planting was not the main pathway. Evaluation continues on this criteria.
The Fruit SEWG commented that the pest was monophagous and recommended that it is only considered for listing on Rubus idaeus, not on all Rubus species. See section pathway.
The Fruit SEWG commented that the pest was monophagous and recommended that it is only considered for listing on Rubus idaeus, not on all Rubus species. See section pathway.
4 - Are the listed plants for planting the main* pathway for the "pest/host/intended use" combination? (*: significant compared to others):
Yes
Conclusion:
Candidate
Justification:
Resseliella theobaldi (raspberry cane midge) is narrowly monophagous on Rubus idaeus (Ellis, 2001-2024). Nijveldt (1963) investigated a range of Rubus spp. to determine the host range of R. theobaldi. Although the midge oviposited on all the tested Rubus spp., the midge could develop into an adult midge only on Rubus caesius, R. idaeus, R. caesius x R. idaeus and R. nessensis. However, to enable the midge to oviposit on these Rubus plants, an artificial cut was made in the stems. Stem of other Rubus spp. hardly ever develop natural splits, only Rubus idaeus, therefore these Rubus spp. are not considered to be important in the population development (Nijveldt, 1963).
This is confirmed by McNicol et al. (1983) who showed that R. parviflorus, R. odoratus and F2 plants from the cross R. crataegifolius x R. idaeus are resistant to Resseliella theobaldi when exposed to the pest in an insectary or in the field and, in Rubus idaeus, the amount and extent of natural splits on the canes characteristic of different varieties seem to be the trait that determines their susceptibility to attack by this pest (Pitcher, 1952; Vetek et al., 2006).
However, according to Gratwick (1992), Resseliella theobaldi occasionally attacks loganberry (Rubus x loganobaccus). Pitcher (1952) also reported that larvae develop on this second host.
The midges overwinter as larvae in soil cocoons in the upper 1-4 cm of the soil. They pupate in spring and emerge as adults from April until June (with considerable geographic variability), depending on the soil temperature and local climate (APS, 2017). Depending on geographic region the midge has 3 or more generations per year. Adults of the second generation emerge in late June to August, usually at a time berry cultivars have developed extensive splits in the bark. Numerous eggs are laid in these splits at the base of the canes. The larvae feed on the newly exposed cane cork (periderm). Once fully grown, they drop to the soil and spin cocoons. In northern areas, these larvae go into diapause, but in warmer regions in central and southern Europe, they may produce a fourth or fifth generation. Adult midges are weak flyers and will only travel short distances. Spread between distant plantations is most likely by the transport of cocoons attached to the roots of new planting material (Gordon & Birch, 2017). Raspberry cane midge larvae can quickly overrun newly established plantations if introduced together with infested planting material or soil (Vetek et al., 2006b). In several countries the insect has been introduced mainly with infested planting materials and somewhere with infested soil (Mohamedova, 2017).
[In the responses to the questionnaire, SI commented that the pest was 'widespread'.]
Considering that the pest was narrowly monophagous, and that adults were flying only short distances, the Fruit SEWG concluded that plants for planting should be considered as significant pathway (with some uncertainty).
This is confirmed by McNicol et al. (1983) who showed that R. parviflorus, R. odoratus and F2 plants from the cross R. crataegifolius x R. idaeus are resistant to Resseliella theobaldi when exposed to the pest in an insectary or in the field and, in Rubus idaeus, the amount and extent of natural splits on the canes characteristic of different varieties seem to be the trait that determines their susceptibility to attack by this pest (Pitcher, 1952; Vetek et al., 2006).
However, according to Gratwick (1992), Resseliella theobaldi occasionally attacks loganberry (Rubus x loganobaccus). Pitcher (1952) also reported that larvae develop on this second host.
The midges overwinter as larvae in soil cocoons in the upper 1-4 cm of the soil. They pupate in spring and emerge as adults from April until June (with considerable geographic variability), depending on the soil temperature and local climate (APS, 2017). Depending on geographic region the midge has 3 or more generations per year. Adults of the second generation emerge in late June to August, usually at a time berry cultivars have developed extensive splits in the bark. Numerous eggs are laid in these splits at the base of the canes. The larvae feed on the newly exposed cane cork (periderm). Once fully grown, they drop to the soil and spin cocoons. In northern areas, these larvae go into diapause, but in warmer regions in central and southern Europe, they may produce a fourth or fifth generation. Adult midges are weak flyers and will only travel short distances. Spread between distant plantations is most likely by the transport of cocoons attached to the roots of new planting material (Gordon & Birch, 2017). Raspberry cane midge larvae can quickly overrun newly established plantations if introduced together with infested planting material or soil (Vetek et al., 2006b). In several countries the insect has been introduced mainly with infested planting materials and somewhere with infested soil (Mohamedova, 2017).
[In the responses to the questionnaire, SI commented that the pest was 'widespread'.]
Considering that the pest was narrowly monophagous, and that adults were flying only short distances, the Fruit SEWG concluded that plants for planting should be considered as significant pathway (with some uncertainty).
5 - Economic impact:
Are there documented reports of any economic impact on the host?
Yes
Justification:
Resseliella theobaldi is one of the most important pests of cultivated red raspberry Rubus idaeus throughout Europe, especially on cultivars fruiting on two-year-old canes (Vetek et al., 2006a; Labanowska and Cross, 2008; Mohamedova, 2017). The direct damage by the midge larval feeding is superficial, but the feeding sites become infected by a range of fungi, resulting in a disease called midge blight. Midge blight is restricted to red raspberry cultivars (Gordon & Birch, 2017).
The infection leads to two types of damage.
- First-generation feeding sites develop deeply penetrating lesions, which give rise to conspicuous cankers. Cankered canes may survive and fruit the following year, but they are physically weakened an may be broken by the passage of machinery, fruit pickers or winds during later in the season.
- The damage arising from the second- and third-generation midges is more serious, because larger numbers of larvae are involved and the fungi that colonize the larval feeding sites penetrate and damage the cork layer, which cannot be repaired at this state of maturity. The production of these splits in relation to the emergens of successive generations of adult midges is the predominant factor in this disease. Cane losses of 50-90% have been recorded in areas where the onset of splitting coincides precisely with the midge emergence (Gordon & Williamson, 2017; Gordon & Birch, 2017).
Yield losses frequently exceed 50%, often making the crop unprofitable to harvest (Gordon et al., 2002).
The infection leads to two types of damage.
- First-generation feeding sites develop deeply penetrating lesions, which give rise to conspicuous cankers. Cankered canes may survive and fruit the following year, but they are physically weakened an may be broken by the passage of machinery, fruit pickers or winds during later in the season.
- The damage arising from the second- and third-generation midges is more serious, because larger numbers of larvae are involved and the fungi that colonize the larval feeding sites penetrate and damage the cork layer, which cannot be repaired at this state of maturity. The production of these splits in relation to the emergens of successive generations of adult midges is the predominant factor in this disease. Cane losses of 50-90% have been recorded in areas where the onset of splitting coincides precisely with the midge emergence (Gordon & Williamson, 2017; Gordon & Birch, 2017).
Yield losses frequently exceed 50%, often making the crop unprofitable to harvest (Gordon et al., 2002).
What is the likely economic impact of the pest irrespective of its infestation source in the absence of phytosanitary measures? (= official measures)
Major
Is the economic impact due to the presence of the pest on the named host plant for planting, acceptable to the propagation and end user sectors concerned?
No
Is there unacceptable economic impact caused to other hosts (or the same host with a different intended use) produced at the same place of production due to the transfer of the pest from the named host plant for planting?
Conclusion:
Candidate
Justification:
Evidence of its economic impact is available in the literature.
6 - Are there feasible and effective measures available to prevent the presence of the pest on the plants for planting at an incidence above a certain threshold (including zero) to avoid an unacceptable economic impact as regards the relevant host plants?
Yes
Conclusion:
Candidate
Justification:
Effective control relies on predicting the accurate date of emergence of the female adult midges and targeting of the insecticide spraying to the base of the primocanes in spring in order to suppress the first generation (Labanowska and Cross, 2008; Tanaskovic and Milenkovic, 2011). Pheromone traps are very useful in monitoring the flight of this insect (Labanowska and Cross, 2008).
Dalman and Malkki (1986) found that the removal of young canes (15-20 cm) reduced the number of larvae and the number of fungal lesions.
Dalman and Malkki (1986) found that the removal of young canes (15-20 cm) reduced the number of larvae and the number of fungal lesions.
7- Is the quality of the data sufficient to recommend the pest to be listed as a RNQP?
Yes
Conclusion:
Candidate
Justification:
CONCLUSION ON THE STATUS:
Recommended for listing as an RNQP, based on data.
8 - Tolerance level:
Is there a need to change the Tolerance level:
No
Proposed Tolerance levels:
9 - Risk management measures:
Is there a need to change the Risk management measure:
No
Proposed Risk management measure:
REFERENCES:
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