EPPO Global Database

Apriona cinerea(APRICI)

EPPO Datasheet: Apriona cinerea

Last updated: 2022-01-04

IDENTITY

Preferred name: Apriona cinerea
Authority: Chevrolat
Taxonomic position: Animalia: Arthropoda: Hexapoda: Insecta: Coleoptera: Cerambycidae
Other scientific names: Apriona newcombei Gilmour
Common names in English: apple stem borer, apple tree borer, poplar stem borer
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EPPO Categorization: A1 list
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EPPO Code: APRICI

HOSTS 2021-12-15

The major hosts of A. cinerea belong to the family Salicaceae (in particular Populus and Salix) and to Morus, Ficus, Prunus and Pyrus species.

Host list: Debregeasia saeneb, Ficus carica, Ficus, Maclura pomifera, Malus domestica, Moringa oleifera, Morus indica, Morus, Populus alba, Populus ciliata, Populus deltoides, Populus nigra, Populus x canadensis, Populus x generosa, Populus yunnanensis, Populus, Prunus persica, Prunus, Pyrus communis, Pyrus, Salix, Ziziphus mauritiana

GEOGRAPHICAL DISTRIBUTION 2021-12-15

A. cinerea is indigenous to the west Himalayan ranges and adjoining areas of India and Pakistan.

Asia: India (Haryana, Himachal Pradesh, Jammu & Kashmir, Punjab, Uttarakhand, Uttar Pradesh), Pakistan

BIOLOGY 2021-12-15

In India, adults emerge between June and September and feed on the bark of green living shoots (Singh & Prasad, 1985). Eggs are laid either on branches or on the main stem. Eggs are laid under the bark, in oviposition slits chewed out by the female. Eggs hatch after 5–7 days.

Larvae bore downward in the trunk but make tunnels to the periphery creating holes at regular intervals through which they periodically eject frass. In the early stages of larval growth these frass expulsion holes are close to each other, but later as the larva matures and grows in size larger frass expulsion holes are formed which are further apart. When the larva enters the bole of large mature trees, the consecutive frass expulsion holes are again closer together. In young plants, larvae may tunnel into the roots.

In the foothills of the Himalayas and the adjoining plains the larva continues feeding until October, but in hills in the Western Himalayas it feeds until November. It remains quiescent throughout winter. It resumes activity in March and continues feeding until winter sets in. In the winter of the second year, it excavates a pupal chamber with coarse wood fibres around it and diapauses as a mature larva. In the following spring the larva transforms into a pupa and by May-June the pupa becomes an immature beetle. In June-September the beetle chews it way out through an emergence hole in the main bole. In the case of young plants in which the pupation has taken place in the root the beetles come up to the ground level where they chew their emergence holes. The life cycle is completed in 2 years. The adult may live up to 35 days.

DETECTION AND IDENTIFICATION 2021-12-15

Symptoms

Adults feed on the bark of shoots which may be girdled and killed. The oviposition scar is conspicuous on an infested stem. Generally, one crescent shaped scar is present on each branch of bigger trees. In young plants resin bleeds from oviposition holes and larval tunnels in the bark may be seen. Larval activity may be recognized by the presence of galleries under the bark and, later, tunnels in the wood. Compared with other borers, larvae of A. cinerea are easier to detect because of the presence of regular frass expulsion holes down the trunk at regular distances of 10–15 mm through which frass is ejected. Each larva makes about 8 to 10 circular expulsion holes. Usually, these holes are on the same side of the trunk (or main stem) and the larva is located near the lower most expulsion hole, as it feeds downwards from top to bottom.

The accumulation of a large amount of ejected frass at the base of the infested trees is a clearly visible sign of the presence of Apriona infestation.

Morphology 

Eggs 

Elongate oval in shape, 7–8 mm long and 3–3.2 mm wide, creamy white, rounded at both ends, front end being broader than the rear end, with hexagonal sculpturing on the surface of the egg visible under the microscope.

Larva 

The larva is a creamy white legless grub, elongate and cylindrical in shape 60–70 mm long with maximum breadth at prothorax. i.e. 12 mm, cuticle is rather leathery especially on prothorax. Head of the larva is elongate, anterior margin of the head is chestnut brown, rather strongly depressed, widest at anterior third and converging posteriorly. There are three pairs of minute legs. Abdomen with dorsal ampullae non-tuberculate, but armed with small chestnut brown asperites (Gardner, 1927; Duffy, 1968; Singh & Prasad, 1985).

Pupa 

Length of the pupa is up to 50 mm and maximum width is up to 18 mm. Antennae extend to second abdominal segment where they are strongly curved downward, elytra and wings extending to abdominal segment 4.

Adult 

The beetle is elongate, 26–50 mm in length, rather narrow, greyish to greyish yellow, due to a dense pubescence; the under surface of the insect is black. There is a median longitudinal impressed line on vertex of head, the front is cleft between the eyes; antenna is slightly longer than the body.

Detection and inspection methods

Visual inspections can be carried out in the field to detect signs of the presence of A. cinerea (see above). For the moment, no efficient trapping systems are available for Apriona spp. (EPPO, 2013).

PATHWAYS FOR MOVEMENT 2021-12-15

There is not much data on the capacity for natural spread of A. cinerea. In India it was considered that new plantations more than 1 km from an infestation site are unlikely to be infested during the first 2 years (Singh & Prasad, 1985).

A. cinerea is not a dry wood borer. However, it survives in logs while wood retains moisture. Diapausing mature larvae may be transported while in their pupal chambers along with felled logs in winter. If these logs are kept under moist conditions and not sawn, then beetles from these logs may emerge in summer and colonize new areas. 

This insect can be transported with plants (including transport as eggs on cuttings) and wood products (including wood, wood packaging, wood chips, firewood) containing bark, moving in international trade.

PEST SIGNIFICANCE 2021-12-15

Economic impact 

The main damage associated with Apriona spp. is caused by the larvae, which bore into the wood soon after hatching, creating long tunnels. Several larvae may be found in a tree. This affects the growth of the trees and decreases the quantity and quality of the timber and longevity of the trees (Shui et al., 2009; Li, 1996). Trees may die and stems/trunks may break. The timber becomes unsuitable for commercial use (e.g. plywood) and entry of fungi and pathogens into the galleries cause discoloration of the wood. The affected trees are much less resistant to wind and may be damaged or fall in moderate winds. Both young and adult trees may become infested. A. cinerea can cause major damage in apple, mulberry and poplar plantations. The adults feed on the bark and cut the leaves and girdle young shoots thus killing them. (Singh & Prasad, 1985). Up to 60% tree mortality has been recorded in young plantations of P. deltoides in Jammu, India (Singh et al., 2004). During random surveys in August-September 2020, less than 0.5% incidence was recorded on P. deltoides clones G-48, WSL109 & WSL 110 under agroforestry in Haryana, Punjab and Uttar Pradesh states of India (A.P. Singh pers. comm., November 2021). This low incidence shows that when good management practices are applied (e.g. use of relatively tolerant clones, isolation from other potentially infested host plants, destroying borer infested trees and timber in the field by burning) the pest can be controlled in poplar plantations.

Control

Control measures include chemical control (including sprays or microcapsules targeting the adults or eggs and young larvae, and fumigation or injections targeting older larvae in trunks and branches), physical control (removal of host trees such as mulberry or paper mulberry on which maturation feeding could occur, or manually catching and killing adults), and biological control (injection of Beauveria bassiana into larval holes, use of parasitic nematodes such as Steinernema spp.). Cultural practices such as sanitation felling (i.e. destruction of damaged and infested plants, or pruning), or use of trap trees, as well as methods to maintain tree vigour help reduce damage.

A. cinerea is a serious pest of apple, mulberry and poplar plantations, hence care should be taken not to grow mulberry or poplar in the vicinity of apple orchards. New plantations should also not be established near infested stands. Potential hosts of the borer must be removed from areas up to 1 km from poplar plantations. In India, the Populus deltoides clone G-48 is relatively tolerant to this pest (Singh et al., 2004).

The natural enemies which have been identified are Steinernema nematodes (Chaudhry & Gul, 1986) and an elaterid beetle, Alaus sp. (Chaudhry & Gul, 1992); a hymenopteran parasitoid Aprostocetus fukutai and Beauveria bassiana (CABI, 2021) and a coleopteran parasitoid Dastarcus helophoroides (Wei et al., 2008). 

Phytosanitary risk

In areas where A. cinerea could establish, the pest would be expected to attack poplars, apples, willows, mulberries and other host plants in the natural environment, commercial orchards, gardens, plantations and urban areas. It is expected that the potential damage would be high in the southern part of the EPPO region where the pest is more likely to establish outdoors, especially if it established in the wild on hosts that occurred extensively with or without management (e.g. poplar). The environmental impact could be major if the pest reaches forests and other environments where poplar or willow are present. However, there is uncertainty as to the extent to which species belonging to host genera that are present in the EPPO region, but not in the area of origin, might be attacked (EPPO, 2013).

PHYTOSANITARY MEASURES 2021-12-15

Experience with other cerambycid beetles in the EPPO region showed that their eradication once introduced is very difficult. Therefore, priority should be given to prevent their entry.

Suggested phytosanitary measures for commodities of host plants include origin from a pest-free area, or a pest-free site under physical protection or treatment (heat or irradiation for wood and chipped to a size smaller than 3 cm for wood chips). Further guidance can be found in the EPPO Standards on commodity-specific phytosanitary measures for Populus and Salix (EPPO, 2017a,b). Wood packaging material should be treated according to ISPM 15.

REFERENCES 2021-12-15

CABI (2021) Apriona cinerea. CABI Crop Protection Compendium. https://www.cabi.org/cpc/datasheet/6508 [last accessed November 2021]. 

Chaudhry MI & Gul H (1986) Some observations on entomophagous Neoaplectana on poplar stem borer, Apriona cinerea Chev. in NWFP. Pakistan Journal of Forestry 42, 214–222. 

Chaudhry MI & Gul H (1992) Some observations on natural enemies of poplar borers in Pakistan. Pakistan Journal of Forestry 36, 119–123. 

Duffy EAJ (1968) A monograph of the immature stages of Oriental timber beetles (Cerambycidae). British Museum Natural History, London (GB), 434 pp. 

EPPO (2013) Pest risk analysis for Apriona germari, A. japonica, A. cinerea. EPPO, Paris (FR). Revised in 2021. https://pra.eppo.int/pra/d27ccfab-df80-4d8f-afcf-0ce8512a89d7 [last accessed November 2021]. 

EPPO (2017a) PM 8/7 Commodity-specific phytosanitary measures. Populus. EPPO Bulletin 47(3), 470-478.

EPPO (2017b) PM 8/7 Commodity-specific phytosanitary measures. Salix. EPPO Bulletin 47(3), 479-486.

Li K (1996) Poplar stem-boring pests and their control. Journal of Northeast Forestry University 7(1), p. 51. 

Shui SY, Wen JB, Chen M, Hu XL, Liu F & Li J (2009) Chemical control of Apriona germari (Hope) larvae with zinc phosphide sticks. Forestry Studies in China 11, 9–13. 

Singh AP, Bhandari RS & Verma TD (2004) Important insect pests of poplars in agroforestry and strategies for their management in northwestern India. Agroforestry Systems 63, 15–26.

Singh P & Prasad G (1985) Poplar stem borer Apriona cinerea Chevrolat (Coleoptera: Cerambycidae) its biology, ecology and control. The Indian Forester 111, 517–524. 

Wei JR, Yang ZQ, Hao HL & Du JW (2008) (R)-(+)-limonen, kairomone for Dastarcus helophoroides, a natural enemy of longhorned beetles. Agricultural and Forest Entomology 10, 323–330.

ACKNOWLEDGEMENTS 2021-12-15

This datasheet was originally drafted by Arun P. Singh, Forest Research Institute, Dehradun, India. It was further elaborated based on the results of the Pest Risk Analysis conducted by an EPPO expert working group in December 2011 (EPPO, 2013). This datasheet was revised in 2021 by Arun P. Singh, Forest Research Institute, Dehradun, India. His valuable contribution is gratefully acknowledged.

How to cite this datasheet?

EPPO (2022) Apriona cinerea. EPPO datasheets on pests recommended for regulation. Available online. https://gd.eppo.int

Datasheet history 2021-12-15

This datasheet was first published in the EPPO Bulletin in 2014 and is now maintained in an electronic format in the EPPO Global Database. The sections on 'Identity', ‘Hosts’, and 'Geographical distribution' are automatically updated from the database. For other sections, the date of last revision is indicated on the right.

EPPO (2014) Apriona cinerea. Datasheets on pests recommended for regulation. EPPO Bulletin 44(2), 151-154. https://doi.org/10.1111/epp.12126