Suchergebnisse

The potato cyst nematodes Globodera pallida and G. rostochiensis are listed in the EU Plant Health Directive 2000/29/EC and are also subject to the new EU Council Directive 2007/33/EC on the control of potato cyst nematodes, requiring unilateral suppression of these pests in Europe. At the same time there is also pressure to increase world trade in potatoes. Such pressure has to be balanced by the risks involved in the associated spread of these pests and subsequent problems in management. Populations of the potato cyst nematodes from outside Europe, in particular South America, which is considered the origin of G. pallida and G. rostochiensis, pose a risk to those European countries where limited genetic variability of these nematode species has been recorded. The development and usage of resistant cultivars under such conditions has formed a pivotal role in integrated management programmes in Europe. Molecular studies have shown that populations of G. pallida and G. rostochiensis from South America have a different genetic composition from those in Europe. The introduction of such populations would pose a threat to the use of resistant cultivars as a major tool in reducing the potential spread and damage caused by these species. At present, an inability to link precisely genetic variability to the virulence characteristics of a specific nematode population, and quickly identify the virulence status of intercepted populations for inspection purposes, strengthens the case for using plant health legislation to prevent their introduction.

Following a request from the European Commission, the EFSA Plant Health Panel performed a pest categorisation of Lopholeucaspis japonica (Hemiptera: Diaspididae), an armoured scale which preferentially feeds on smooth barked woody trees and shrubs. The pest occurs in Asia, North America and non-EU Europe (Caucasus region and Ukraine). The pest is regulated in Council Directive 2000/29/EC as Leucaspis japonica, a junior synonym. Its introduction into the EU is banned on plants of Citrus, Fortunella, Poncirus and their hybrids, other than fruit and seeds. Additional host plants comprise 60 species in 35 botanical families, including deciduous fruit trees, ornamental and forest plants. L. japonica could enter the EU via host plants for planting (excluding seeds) and cut branches. It has been intercepted on plants for planting from China, including artificially dwarfed plants. Spread is most likely via plants for planting, rather than via natural spread as most diaspidid life stages are sessile. Impacts could occur in citrus, other fruit crops, ornamentals and forest trees. Sourcing plants from pest-free areas, pest-free places of production or pest-free production sites would decrease the likelihood of introduction. Because suitable hosts occur across the EU in climatic areas matching those where the pest is known to occur, biotic and abiotic conditions are conducive to establishment. The main uncertainty concerns its current distribution in the EU. L. japonica was found in Greece in 1983, but there have been no other reports since then. L japonica satisfies the criteria assessed by EFSA that enable it to be considered a potential quarantine pest. L. japonica does not satisfy the criteria assessed by EFSA for it to be considered a potential regulated non-quarantine pest (RNQP).

The Panel on Plant Health performed a pest categorisation of nematodes belonging to the genus Hirschmanniella (Nematoda: Pratylenchidae). Twenty-nine species in this genus have been considered of which five species are present in the EU (Hirschmanniella behningi, Hirschmanniella gracilis, Hirschmanniella halophila, Hirschmanniella loofi and Hirschmanniella zostericola). The whole genus except H. gracilis is regulated by Council Directive 2000/29/EC (Annex IAI). Hirschmanniella species are root endoparasites uniquely adapted to aquatic environments. Most species are reported from tropical regions. Monocotyledons including aquatic plants are main hosts and some Hirschmanniella species are important pests of rice. Plants for planting are potential pathways for entry. Hirschmanniella species are frequently intercepted on imported aquarium plants. Measures are available to avoid entry. Environmental conditions in greenhouses and potentially in rice production areas of the EU are suitable for establishment. The nematode may be spread with irrigation, tools or plants for planting. Hirschmanniella species were categorised into four groups. The first group includes species reported as pests of crop plants; those satisfy all the criteria that are within the remit of EFSA to assess to be regarded as Union quarantine pests. The second group includes species that are not reported to cause economic damage to crop plants; those species do not satisfy all the criteria to be regarded as Union quarantine pests. Uncertainty exists whether species in this group can cause damage once introduced into the EU. The third group includes species that are known to be present in the EU and do not cause damage; they do not satisfy the criteria to be regarded as Union quarantine pests or regulated nonquarantine pests. The fourth group consists of H. gracilis only. This worldwide occurring species is present in the EU where it does not cause economic damage. It does not satisfy all the criteria to be regarded as a Union quarantine pest.

The Panel on Plant Health performed a pest categorisation of Xiphinema americanum sensu lato (Nematoda: Longidoridae) for the EU. Sixty-one species in this group are recognised. They are polyphagous pests found in soil associated with a number of plant species. As a migratory ectoparasitic species, it punctures cells of plant roots. Nematodes were classified in four categories based on their distribution and ability to transmit viruses. Category I contains the seven virus vector species present outside the EU: X. americanum sensu stricto, X. bricolense, X. californicum, X. inaequale, X. intermedium, X. rivesi (non-EU populations) and X. tarjanense. Category II contains the 28 species not present in the EU and not known to transmit any virus. Twenty-six species are present in the EU and are not known to be virus vectors (category III). Category IV contains the species present in the EU, which is a virus vector (EU populations of X. rivesi). All nematodes known to be virus vectors occurring outside the EU (category I) satisfy all the criteria that are within the remit of EFSA to assess to be regarded as Union quarantine pests. This is mainly due to their association with non-EU virus isolates. Categories II and III contain species that are not reported to transmit viruses or cause economic damage to crop plants. Although uncertainty concerning their ability to transmit viruses exists, those species do not satisfy all the criteria to be regarded as Union quarantine pests. Category IV contains the EU populations of X. rivesi. The species is a virus vector but current EU populations of X. rivesi have not been reported to be associated with any of the EU viruses or their non-EU isolates under field conditions. Xiphinema rivesi (EU populations) is widespread in some Member States and does not satisfy all the criteria to be regarded as a Union quarantine. None of the species can be regarded as a regulated non-quarantine pest.

The Panel on Plant Health performed a pest categorisation of the gall midge Aschistonyx eppoi Inouye (1964) (Diptera, Cecidomyiidae), for the EU. A. eppoi is a well-de fi ned and distinguishable species, native to Japan and Korea, and recognised as a pest of Juniperus chinensis , although our knowledge is solely based on one unique publication. A. eppoi is absent from the EU, and is listed in Annex IIAI of Directive 2000/29/EC. Its host plants, Juniperus spp. are also listed in Annex III of Directive 2000/29/EC. Plants for planting and branches are considered as pathways for this pest. A. eppoi has been intercepted twice (1974; 1975) in the EU and has been eradicated. The pest is likely to affect bonsai plants of J. chinensis if it were to establish in the EU territory. However, as it is unknown whether A. eppoi would attack the Juniperus spp. that occur in the EU, its potential impact on the wild vegetation is also unknown. As the pest originates from areas with warm climates, impact outdoors would affect the southern parts of the EU. Cultural control (destruction of infested material) and chemical control are the major control methods. All criteria assessed by EFSA for consideration as a potential quarantine pest are met, although there are high uncertainties regarding impact. The species is presently absent from the EU, and thus the criteria for consideration as a potential regulated non-quarantine pest are not met.

The Panel on Plant Health performed a pest categorisation of the citrus snow scale, Unaspis citri (Comstock) (Hemiptera: Diaspididae), for the European Union (EU). This is a well-de fi ned and distinguishable species, native to south-eastern Asia, which has spread to many tropical and subtropical regions. U. citri can be a pest of citrus and has been cited on over 28 different species in 16 plant families. In the EU, U. citri occurs in the Azores. There is uncertainty as to whether it occurs in continental Portugal. Reports of it occurring in Greece and Spain are likely to be invalid and based on interception records from these countries. An old Italian record is a misidenti fi cation. U. citri is listed in Annex IIAI of 2000/29/EC as a harmful organism. The international trade of hosts, as either plants for planting, fruit or cut fl owers, provide potential pathways into the EU. However, current EU legislation prohibits the import of citrus plants for planting from third countries. U. citri is mostly con fi ned to coastal humid tropical areas and does not occur in semi-arid areas that are irrigated. Nevertheless, given that it occurs in the Azores and that there are regional climatic similarities between places where U. citri occurs and climates within the EU, and taking EU host distribution into account, U. citri has the potential to establish in the EU, especially in citrus-growing regions around the Mediterranean where losses in quality and yield of citrus could occur. Phytosanitary measures are available to inhibit the likelihood of introduction of U. citri . Considering the criteria within the remit of EFSA to assess the status as a potential Union quarantine pest (QP), or as a potential regulated non-quarantine pest (RNQP), U. citri meets the criteria assessed by EFSA for consideration as a potential Union QP.

The Panel on Plant Health performed a pest categorisation of the weevil Anthonomus quadrigibbus Say, (Coleoptera: Curculionidae), for the EU. A. quadrigibbus is a well-de fi ned and distinguishable species, recognised as an occasional pest of apples, pears and sour cherries in North America where it also feeds on a range of wild rosaceous plants such as Crataegus and Amelanchier . Adults feed on leaves, fl owers and fruit. Feeding damage to fruit reduces quality. Females oviposit into young fruit, causing surface blemishes and resulting in distortion as the fruit develops. Marketability is subsequently reduced. Larvae and pupae develop within host fruit. Most infested fruit fall prematurely, reducing yield. A. quadrigibbus was regarded as a more serious pest in the early 20th century. A. quadrigibbus is not known to occur in the EU and is listed in Annex IIAI of Council Directive 2000/29/EC under the synonym Tachypterellus quadrigibbus . Host plants for planting and infested fruit could potentially provide a pathway into the EU. Considering the climatic similarities between North America and Europe, and that wild and commercial hosts occur widely within the EU, A. quadrigibbus has the potential to establish within the EU. There would be one generation per year, as in North America. Impacts could be expected in apple, pear and perhaps sour cherry orchards. The level of impacts would be uncertain. There is also uncertainty regarding whether A. quadrigibbus would extend its host range to include other Rosaceae within the EU. Phytosanitary measures are available to reduce the likelihood of introduction of A. quadrigibbus . All criteria assessed by EFSA for consideration as a potential Union quarantine pest are met. As A. quadrigibbus is not known to occur in the EU, this criterion assessed by EFSA to consider it as a Union regulated non-quarantine pest is not met.

The EFSA Panel on Plant Health performed a pest categorisation of Cadang-Cadang viroid for the European Union (EU) territory. Coconut cadang-cadang viroid (CCCVd) is a well-known viroid for which efficient molecular detection assays are available. It is transmitted by vegetative multiplication of infected hosts, by seed and pollen and, possibly, by the action of unknown vector(s). CCCVd is reported from a few countries in Asia and is not known to occur in the EU. It therefore does not meet one of the criteria for being a Union regulated non-quarantine pest. The host range of CCCVd is restricted to Arecaceae species (palms), in particular coconut and it is listed on all known hosts in Annex IIAI of Directive 2000/29/EC. CCCVd is expected to be able to enter in the EU and to be able to establish in the open in the southernmost regions of the EU and elsewhere under protected cultivation. It has the potential to subsequently spread via plants for planting and possibly other mechanisms. CCCVd is able to cause severe symptoms in some Arecaceae species while others seem less affected. The potential impact of CCCVd if introduced in the EU is very difficult to assess. Given that the spread potential is, as for other viroids, likely to be limited, the potential impact is estimated to be limited in extent but this judgement is affected by large uncertainties. Overall, CCCVd meets all the criteria evaluated by EFSA to qualify as Union quarantine pest. The main knowledge gaps concern (1) the relationships between CCCVd-related RNAs and CCCVd, (2) the origin and volume of the trade in palm seeds and plants for planting imported in the EU (3) the efficiency of natural spread under EU conditions and (4) host status and susceptibility of many palm species grown in the EU.

The EFSA Panel on Plant Health performed a pest categorisation of non-EU isolates of the Little cherry pathogen (LCP) for the European Union (EU) territory. LCP is now known to be in fact two distinct, well characterised viruses, Little cherry virus 1 (LChV1) and Little cherry virus 2 (LChV2) collectively referred to here as LChV. Efficient molecular detection assays are available for both viruses but not to discriminate EU and non-EU isolates. LChV are transmitted by vegetative multiplication of infected hosts and, for LChV2, by mealybug vectors. LChV are reported from a range of countries, both outside and within the EU. Non-EU isolates are not known to occur in the EU and therefore do not meet one of the criteria for being a Union regulated non-quarantine pest. The host ranges of LChV are restricted to Prunus species, in particular cultivated and ornamental cherries. LChV non-EU isolates are listed for some, but not all hosts, in Annex IIAI of Directive 2000/29/EC. LChV isolates are expected to be able to enter and establish in the EU. They have the potential to subsequently spread through plants for planting and, for LChV2, through the action of the Phenacoccus aceris vector, which is present in many EU MS. LChV are able to cause severe symptoms in some cherry varieties while others are less affected. Overall, non-EU LChV isolates meet all the criteria evaluated by EFSA to qualify as Union quarantine pests. However, given the currently limited impact of EU LChV isolates, the impact of non-EU isolates, if introduced, could be similarly limited. The main knowledge gaps and uncertainties concern (1) whether EU and non-EU isolates of LChV might differ in their biology, epidemiology or symptomatology, (2) efficiency of natural spread by vectors under EU conditions and (3) extent of symptoms caused on many EU-grown varieties.

The Panel on Plant Health performed a pest categorisation of the South African citrus thrips, Scirtothrips aurantii Faure (Thysanoptera: Thripidae), for the European Union (EU). This is a well-de fi ned and distinguishable species, recognised as a pest of citrus and mangoes in South Africa, which has been cited on more than 70 different plants, including woody and herbaceous species. It feeds exclusively on young actively growing foliage and fruit. S. aurantii is not known to occur in the EU and is listed in Annex IIAI of 2000/29/EC as a harmful organism presenting a risk to EU plant health. The international trade of hosts as either plants for planting or cut fl owers provide potential pathways into the EU. However, current EU legislation prohibits the import of citrus plants. Furthermore, measures aimed at the import of plants for planting in a dormant stage (no young foliage or fruits present) with no soil/growing medium attached, decreases the likelihood of the pest entry with such plants. Interceptions have occurred on Eustoma grandi fl orum cut fl owers. Considering climatic similarities between some of the countries where S. aurantii occurs (South Africa, Australia) and the EU, its thermal biology and host distribution in the EU, S. aurantii has the potential to establish, especially in citrus-growing regions of the EU. S. aurantii would most probably breed all year long around the Mediterranean and could cause crop losses in citrus, especially oranges. Phytosanitary measures are available to inhibit the introduction of S. aurantii . Considering the criteria within the remit of EFSA to assess its status as a potential Union quarantine pest (QP) or as a potential regulated non-quarantine pest (RNQP), S. aurantii meets with no uncertainties the criteria assessed by EFSA for consideration as a potential Union QP

The Panel on Plant Health performed a pest categorisation of the citrus thrips, Scirtothrips citri (Moulton) (Thysanoptera: Thripidae), for the European Union (EU). This is a well-de fi ned and distinguishable species, occurring in North America and Asia. Its precise distribution in Asia is uncertain. S. citri is a pest of citrus and blueberries and has been cited on over 50 different host species in 33 plant families. Whether all plants reported as hosts are true hosts, allowing population development of S. citri , is uncertain. S. citri feeds exclusively on young actively growing foliage and fruit. It is not known to occur in the EU and is listed in Annex IIAI of 2000/29/EC as a harmful organism. The international trade of hosts, as either plants for planting or cut fl owers, provide potential pathways into the EU. However, current EU legislation prohibits the import of citrus plants for planting. Furthermore, measures aimed at the import of plants for planting in a dormant stage (no young foliage or fruits present) with no soil/growing medium attached, decreases the likelihood of the pest ' s entry via other hosts. Considering that there are regional climatic similarities where S. citri occurs in the USA with climates in the EU, and taking EU host distribution into account, S. citri has the potential to establish in the EU, especially in citrus and blueberry growing regions around the Mediterranean where quality losses in citrus and yield losses in blueberry could occur. Phytosanitary measures are available to inhibit the likelihood of introduction of S. citri from infested countries. Considering the criteria within the remit of EFSA to assess its status as a potential Union quarantine pest (QP) or as a potential regulated non-quarantine pest (RNQP), S. citri meets with no uncertainties the criteria assessed by EFSA for consideration as a potential Union QP.

The Panel on Plant Health performed a pest categorisation of the Siberian moth, Dendrolimus sibiricus Tschetverikov (Lepidoptera: Lasiocampidae). D. sibiricus is a well-defined and distinguishable species, native to Asian Russia and northern regions of Kazakhstan, Mongolia, China and North Korea, and recognised as a severe pest of Pinaceae conifers, mainly larch (Larix spp.), fir (Abies spp.), spruce (Picea spp.), five-needle pines (Pinus spp.). It has also a potential to develop on non-native Pinaceae: Cedrus, Pseudotsuga, Tsuga. It defoliates healthy trees and kills thousands of hectares of forests. It is absent from the EU and is listed as a quarantine pest in Annex IAI of Directive 2000/29/EC. Plants for planting, branches of conifers and non-squared wood from its distribution range are considered as pathways for the pest, which can also disperse by flight over tens of kilometres. The females produce sex pheromones. Adults do not feed and can survive for about 2 weeks. One female lays up to 400 eggs, attaching them to needles. One generation usually develops in 2–3 years, with larvae passing winter diapause and some undergoing facultative summer diapause. Exceptionally, 1-year generations may occur if the number of degree-days above 10°C is higher than 2,200. Larvae feed on needles through 5–6 instars and pupate in a cocoon on tree branches. Mature larvae have urticating setae on thoracic segments that protect them from enemies and may cause allergic reactions in humans and animals. The contradictory studies regarding the climatic requirements of D. sibiricus make the issue of its establishment in most of the EU territory uncertain, although its host trees are widely present. All criteria for considering D. sibiricus as a potential quarantine pest are met. The species is presently absent from the EU, and thus, the criteria for consideration as a potential regulated non-quarantine pest are not met.

Following a request from the European Commission, the EFSA Panel on Plant Health performed a pest categorisation of Guignardia laricina , a well-de fi ned and distinguishable fungal species of the family Phyllostictaceae. The pathogen is regulated in Council Directive 2000/29/EC (Annex IAI) as a harmful organism whose introduction into the EU is banned. G. laricina is native to East Asia and causes a shoot blight disease of Larix spp. Major hosts of G. laricina are European larch ( Larix decidua ) and two North American larch species ( Larix laricina (tamarack) and Larix occidentalis (Western larch)). Larix kaempferi (Japanese larch) is reported as susceptible. The only other host in nature is Douglas fi r ( Pseudotsuga menziesii) , which is reported as an incidental host, but various other conifers have been reported as susceptible following arti fi cial inoculation, including Picea abies . The fungus is not known to occur in the EU but could enter via plants for planting (including arti fi cially dwarfed plants) and cut branches of Larix spp. It could establish in the EU, as hosts are present and climatic conditions are favourable. The pathogen would be able to spread following establishment by natural dissemination of ascospores and pycnospores and by human movement of infected plants for planting. Should the pathogen be introduced in the EU, impacts can be expected in larch forests, plantations and nurseries, leading to reduced tree growth and ecosystem service provision. The key uncertainties concern the current distribution and level of impacts in the native range of the pathogen. The criteria assessed by the Panel for consideration as a potential quarantine pest are met. As the pest is not present in the EU, not all criteria for consideration as a regulated non-quarantine pest are met.

The Panel on Plant Health performed a pest categorisation of the fungus Synchytrium endobioticum, the causal agent of potato wart disease, for the European Union (EU). The identity of the pest is well established and reliable methods exist for its detection and identification. S. endobioticum is present in most continents. The pest is listed in Annex IAII of Directive 2000/29/EC and is present with a restricted and fragmentary distribution in the EU. The major host is Solanum tuberosum (potato), but in Mexico, the pest also affects wild Solanum spp. S. endobioticum could potentially enter the EU through multiple pathways associated with soil as substrate for non-host plants, contaminant or commodity. The presence of the pest in 16 EU Member States characterised by different climatic conditions suggests that it could establish in the rest of the EU. The disease induces the formation of warts on potato tubers, stolons and stem bases reducing plant growth and yield and making tubers unmarketable. Additional losses may occur during storage. The only available strategy to control the disease and prevent it from spreading is the application of strict phytosanitary measures and the cultivation of potato varieties resistant to the pathotype(s) present in the infested field(s). Specific phytosanitary measures exist (Council Directive 69/464/EEC) for the control of potato wart disease in the EU. The main uncertainties refer to the distribution and host range of the pest, and the importance of some pathways of entry. S. endobioticum meets all the criteria assessed by EFSA for consideration as potential Union quarantine pest. The criteria for considering S. endobioticum as a potential Union regulated non-quarantine pest are not met since, in addition to potato seed tubers, soil (as commodity, substrate or contaminant) and ware potato tubers are major means of spread.