EPPO Alert List – Neodiprion abietis (Hymenoptera: Diprionidae)
Balsam fir sawfly
In October 2016, the NPPO of the Netherlands intercepted Neodiprion abietis (Hymenoptera: Diprionidae – balsam fir sawfly) on cut branches of Gaultheria imported from the USA. As N. abietis does not occur in the EPPO region and is causing severe defoliation on conifers in parts of North America, the Dutch NPPO suggested that N. abietis should be added to the EPPO Alert List. This proposal was supported by the EPPO Panels on Phytosanitary Measures and on Quarantine Pests for Forestry.
Adult female (lateral view)
Courtesy: National Reference Centre, Wageningen (NL)
Courtesy: National Reference Centre, Wageningen (NL)
N. abietis is native to North America and occurs in Southern Canada and Northern United States.
EPPO region: Absent. A pupa of N. abietis was intercepted in 2016 by the Dutch NPPO on a consignment of cut branches of Gaultheria sp. (a non-host) imported from the USA.
North America: Canada (Alberta, British Columbia, Manitoba, New Brunswick, Newfoundland, Nova Scotia, Ontario, Québec, Saskatchewan), Saint-Pierre-et-Miquelon (FR), USA (California, Connecticut, Maine, Minnesota, Missouri, New Hampshire, Wisconsin).
On which plants
The main host is Abies balsamea (balsam fir) but other conifer species have been reported as host plants. In Canada, N. abietis mainly feeds on A. balsamea and occasionally on spruce (Picea glauca and P. mariana). In the literature, other conifer species are mentioned (e.g. Abies amabilis, A. concolor, A. grandis, A. magnifica, A. lasiocarpa, Picea engelmanii, P. sitchensis and Pseudotsuga menziesii) and it has been hypothetized that N. abietis is a species complex, as differences in life histories and host-plant selection for oviposition and feeding have been observed between different populations.
N. abietis is a tree defoliator whose larvae feed on 1 or 2-year old needles. It has been shown that N. abietis preference for, and performance on current-year foliage was very low, it peaked on 2 or 3-year-old foliage, and declined on older foliage. Larvae feed on the outside of the needles, leaving a central portion which then shrivels, turns yellow to brick red, and finally drops off. Feeding on needles of the previous years (and not on the new needles) causes a distinctive browning of the inner canopy. These feeding activities lead to sparse foliage and reduced tree vigour. Severe and repeated defoliation may lead to tree mortality (e.g. after 3 to 5 years of continuous defoliation).
N. abietis has one generation per year, and overwinters as the egg stage. Depending on climatic conditions, adults emerge from late July to early September, and resemble small wasps with four membranous wings. Females are brown (6-8 mm long), males are black (4-5 mm long). Females lay white, oval-shaped eggs in slits cut in the needles. Hatching takes place in May or June. Larvae are gregarious and have green bodies with dark stripes and black heads. Mature larvae (in July or August) are 20 mm long. After the last moult, larvae spin reddish-brown cocoons in the litter on the ground, and less frequently on the foliage.
More pictures can be viewed on the INTERNET:
Adult females of N. abietis can fly but no data is available on their flight capacity. Over long distances, trade of infested host plants can spread the pest. Interestingly, the plant on which N. abietis was intercepted, Gaultheria sp., has never been reported to be a host of N. abietis but can obviously transport it. The NPPO of the Netherlands noted that high numbers of cut branches of Gaultheria sp. are imported from the Northwestern part of North America to be used in flower bouquets. These cut branches are also commonly harvested from the forest understory in Canada.
Plants for planting, cut branches of host plants or non-host plants (such as Gaultheria) transporting live stages (e.g. pupae) from countries where N. abietis occurs.
In parts of Canada and the USA, N. abietis is considered to be a serious forest pest causing reduction of tree vigour, yield losses in the production of wood, and in some cases tree mortality. N. abietis is also considered to be a pest of conifers grown for ornamental purposes or for the production of Christmas trees. During the last decades, the intensity and duration of N. abietis outbreaks has increased in some areas of North America. In the past, periodic outbreaks of N. abietis were localised and of short duration (typically occurring every 5 to 15 years and lasting 4 to 5 years), but outbreaks observed more recently in Western Newfoundland and Nova Scotia encompass extensive areas. For example, from 1991 to 2008, a total area of approximately 560 000 ha was moderately to severely defoliated in Western Newfoundland. Studies conducted in the 2000s have shown that defoliation was favoured by some forest practices, (e.g. pre-commercial thinning). In order to reduce effects of defoliation, biological control programmes with nucleopolyhedrovirus have been developed in Canada. In the EPPO region, Abies spp. are important forest trees but European Abies species differ from the North American ones, and their susceptibility to N. abietis is currently not known. However, some North American species (e.g. A. grandis) have been introduced for wood production in the EPPO region, as well as for ornamental purpospes. It should also be noted that currently, EU member states prohibit the imports of live conifers (other than seeds) from North America, which closes the ‘plants for planting’ pathway. The fact that N. abietis can be transported on non-host plants adds to the risk of introducing this species into the EPPO region. The potential for establishment of N. abietis in the EPPO region remains to be further studied but seems likely, considering the similarities of N. abietis with the European pine sawfly, N. sertifer.
Craighead FC (ed) (1950) Insect enemies of Eastern forests. USDA Miscellaneous Publication no. 657, 679 pp.
Cunningham JC (1984) Neodiprion abietis (Harris), balsam fir sawfly (Hymenoptera: Diprionidae). In: Kelleher JS & Hulme MA (eds) Biological control programmes against insects and weeds in Canada 1969-1980. CABI, Wallingford (GB), 403 pp.
Duffy SP, Young AM, Morin B, Lucarotti CJ, Koop BF, Levin DB (2006) Sequence analysis and organization of the Neodiprion abietis nucleopolyhedrovirus genome. Journal of Virology 80(14), 6952-6963.
Graves R, Lucarotti CJ, Quiring DT (2012) Spread of a Gammabaculovirus within larval populations of its natural balsam fir sawfly (Neodiprion abietis) host following its aerial application. Insects 3, 912-929. doi:10.3390/insects3040912
Huber JT, Moreau G (2003) New synonymy and new sawfly host records for Cirrospilus vittatus (Hymenoptera: Eulophidae) in North America. Canadian Entomologist 135(5), 669-676 (abst.).
Iqbal J, Maclean DA, Kershaw JA Jr (2011) Balsam fir sawfly defoliation effects on survival and growth quantified from permanent plots and dendrochronology. Forestry (Oxford) 84(4), 349-362.
- Government of Canada. Natural Resources Canada. Balsam fir sawfly. https://tidcf.nrcan.gc.ca/en/insects/factsheet/6564
- Préfet de Saint-Pierre-et-Miquelon. Bilan comptage Pestes forestières 2015. http://www.saint-pierre-et-miquelon.developpement-durable.gouv.fr/IMG/pdf/2015_Bilan-comptage-pestes-forestieres_DTAM.pdf
Knerer G, Atwood CE (1972) Evolutionary trends in the subsocial sawflies belonging to the Neodiprion abietis complex (Hymenoptera: Tenthredinoidea). American Zoologist 12(3), 407-418.
Li SY (2011) Major insect pests of Christmas trees in Canada. Proceedings of the 10th International Christmas Tree Research and Extension Conference (IUFRO) (Eichgraben, AT, 2011-07-21/27), 104-109.
Lucarotti CJ, Whittome-Waygood BH, Levin DB (2011) Histology of the larval Neodiprion abietis (Hymenoptera: Diprionidae) digestive tract. Psyche Article ID 910286. doi:10.1155/2011/910286
Moreau G (2006) Past and present outbreaks of the balsam fir sawfly in western Newfoundland: an analytical review. Forest Ecology and Management 221(1/3), 215-219.
Moreau G, Lucarotti CJ, Kettela EG, Thurston GS, Holmes S, Weaver C, Levin DB, Morin B (2005) Aerial application of nucleopolyhedrovirus induces decline in increasing and peaking populations of Neodiprion abietis. Biological Control 33(1), 65-73.
Moreau G, Quiring DT (2011) Stand structure interacts with previous defoliation to influence herbivore fitness. Forest Ecology and Management 262(8), 1567-1575 (abst.).
Moreau G, Quiring DT, Eveleigh ES, Bauce É (2003) Advantages of a mixed diet: feeding on several foliar age classes increases the performance of a specialist insect herbivore. Oecologia 135(3), 391-399 (abst).
NPPO of the Netherlands (2017-03-17) Quick Scan (QS. Ent.2017.001) on Neodiprion abietis, 6 pp. https://www.nvwa.nl/binaries/nvwa/documenten/risicobeoordeling/plantenziekten/archief/2017/quickscan-neodiprion-abietis/Quickscan+Neodiprion+Abietis.pdf
Ostaff DP, Piene H, Quiring DT, Moreau G, Farrell JCG, Scarr T (2006) Influence of pre-commercial thinning of balsam fir on defoliation by the balsam fir sawfly. Forest Ecology and Management 223, 342-348.
EPPO RS 2017/095
Entry date 2017-05