Balsam fir sawfly
Larvae eating fir needles
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Suborder: Symphyta
Family: Diprionidae
Genus: Neodiprion
Species:
N. abietis
Binomial name
Neodiprion abietis
(Harris, 1841)

Neodiprion abietis, commonly known as the balsam fir sawfly, is a species of insect in the family Diprionidae. It is found in North America from Canada to northern Mexico and is phytophagous, feeding on the needles of coniferous trees.[1][2]

Evolutionary relationship

N. abietis is considered to arise from a monophyletic group.[3]

Internal anatomy

The larva of N. abietis have salivary glands with a lumen that is lined by microvilli and it also has a single layer of epithelial cells present. Moreover, they have fat body cells against the anterior duct of the lumen. Balsam fir sawfly have a pair of diverticular pouches which are used to store terpenoids which they regurgitate as a form of defense. These pouches are lined with a layer of an impermeable cuticle. The amount of liquid regurgitated is a reflection of the food that they ingest. The rectum of the Neodiprion abietis larva has a rectum similar to other Diprionidae. The rectum consists of a thin cuticle, a single layer of epithelial cells, and contains muscles.[4]

Physical characteristics

The heads of instars differ in color, newly hatched first instars have a light brown head and prior to molting into second instars, their heads change to a dark brown color. Their heads then turn black in color during the second to fifth instars. A range of 0.48 mm to 0.60 mm is seen with the size of head capsules. The stripes on their body also differ in larval instars. The first and second instar lack longitudinal stripes. The third, fourth, and fifth instar has three pairs of longitudinal dark stripes. The stripes on the third instar are considerably shorter than the fourth and fifth instar, while the stripes of the fourth and fifth instar are very similar causing difficulty for differentiating. The body color and length also varies between instars. Initially, a translucent body is seen, then becomes light green during the first instars. The body length rages anywhere from 2.43 mm to 3.15 mm. The antennas, more specifically their segments, differ between male and female. Male antennas consist of 21-23 segments while female antennas consist of 18-20 segments.[5]

Life cycle

In Newfoundland, Canada, female sawflies lay their eggs in late September or early October using their saw-like ovipositor into foliage of the current year or foliage of the previous year. The different strains of N. abietis are known to differ in host plant oviposition preference.[1][6] Months later, around June or mid-July, the eggs hatch and the larvae feed immediately on needles of the balsam fir. The larvae prefer to eat 2 or 3-year-old balsam fir foliage and will rarely feed on foliage of the current year.[7] The development of male and female sawfly vary slightly. Females can have five or six instars whereas males only have five instars. Secondly, females take slightly longer than males to complete their development. A female's developmental period lasts 35 days whereas males complete their development within 30 days. Male and female sawflies spin a cocoon during their last-instar larva, they pupate inside, and adults emerge from the cocoon within 2–3 weeks. Account differs concerning whether N. abietis will spin its cocoon on the foliage or in the ground.[8][9]

Reproduction

Mated females can produce male and female offspring while unmated females can only produce male offspring, a form of parthenogenesis known as arrhenotoky.[4]

Feeding

The balsam fir sawfly feeds on Abies balsamea, a type of fir, Picea glauca, Picea mariana types of spruce, and Larix laricina, a larch.[10] The first instar feeds on the whole crown of one-year-old foliage following egg hatch and the larvae in a group feed together by moving from one shoot to another.[11] Females, however, have a greater sensitivity to foliage than males and it’s suspected that it is due to their longer developmental time. N. abietis larvae have optimal development when they are able to feed on different-aged foliage thus allowing for maximization of their resources.[7][12] Moreover, the balsam fir sawfly are considered to be wasteful feeders because only the outer portions of needles are consumed during the early-instar larvae. Late instars, however, consume more needle tissue type but it never consumes the needle in its entirety.

Ecological importance

In eastern Canada, local outbreaks of N. abietis can last anywhere from 3 years to 5 years and have been shown to have a periodicity of about 10 years.[13] Ecological factors involved in N. abietis outbreaks are increased immigration, female-biased sex ratios, and reduced mortality due to diseases, parasitoids and host-plant effects.[14][15][16][17]

The outbreaks of the balsam fir sawfly cause a reduction in tree growth which in turn can cause tree mortality.[18][19] The balsam fir sawfly, more specifically third to fifth instar larvae are responsible for defoliation and foliage weight loss in trees. Balsam fir sawfly defoliation does not stimulate the release of buds or shoots, which contributes to a slow recovery and severe impact on the balsam fir.[10] N. abietis outbreaks have been documented to increase in intensity in thinned forests of Atlantic Canada.[15][16][13][18][19][20][21]

Balsam fir outbreaks can be shortened by the application of a baculovirus known as nucelopolyhedrovirus (NeabNPV),[22][23] which has been shown to be involved in the natural decline of balsam fir sawfly outbreaks.[14][15] NeabNPV works by infecting the epithelial cells of the larvae midgut, this infection can be carried within the midgut through to adulthood.[24] Neemix, an insect growth regulator has also been used to slow down larval and pupal development by decreasing pupal weight, and can reduce the ability of the adults to emerge from their cocoon.[25]

References

  1. 1 2 G. Knerer, C.E. Atwood (1973). Diprionid sawflies: polymorphism and speciation. Changes in diapause and choice of food plants led to new evolutionary units. Science, USA, 179(4078), 1090-1099.
  2. González-Gaona, Ernesto; Gómez-Nísino, Alejandro; De Lira-Ramos, Karla Vanessa; Rodríguez-Cruz, Yahaira Elizabeth; Olivo-Martínez, Juan Antonio; Rascón-Mendoza, Ana Adeliz; Sánchez Martínez, Guillermo (2021-02-28). "Primer registro documentado de Neodiprion abietis (Harris, 1841) (Hymenoptera: Diprionidae) para México". Revista Mexicana de Ciencias Forestales. 12 (64). doi:10.29298/rmcf.v12i64.837. ISSN 2448-6671.
  3. C.R. Linnen and B.D. Farrell (2008). Phylogenetic Analysis of Nuclear and Mitochondrial Genes Reveals Evolutionary Relationships and Mitochondrial Introgression in the Sertifer Species Group of the Genus Neodiprion (Hymenoptera: Diprionidae) Molecular Phylogenetics and Evolution. 48(1): 240-257.
  4. 1 2 C.J. Lucarotti, H.W.W. Beatrixe, and D.B. Levin (2011). Histology of the Larval Neodiprion abietis (Hymenoptera: Diprionidae) Digestive Tract. Journal of Entomology. 2012: 1-10.
  5. S. Li (2003). Notes on larval instars and adult antennae of Neodiprion abietis (Hymenoptera : Diprionidae). Canadian Entomologist. 135(5): 745-748.
  6. R.C. Johns, J. Fidgen, and D.P. Ostaff (2013). Host–tree oviposition preference of balsam fir sawfly, Neodiprion abietis (Hymenoptera: Diprionidae), in New Brunswick, Canada. Canadian Entomologist. 145(4): 430-434.
  7. 1 2 G. Moreau, D.T. Quiring, E.S. Eveleigh, E. Bauce (2003). Advantages of a Mixed Diet: Feeding on Several Foliar Age Classes Increases the Performance of a Specialist Insect Herbivore. Oecologia. 135: 391–399.
  8. W. J. Carroll (1962). Some aspects of the Neodiprion abietis (Harr.) complex in Newfoundland. PhD dissertation, Syracuse University, Syracuse, New York, USA.
  9. D.R. Wallace and C.R. Sullivan (1973). Photoperiodism in the Early Balsam Strain of the Neodiprion abietis Complex (Hymenoptera: Diprionidae). Canadian Journal of Zoology. 52: 507-513.
  10. 1 2 P.D. Simon, M.Y Aaron, B. Morin, C.J. Lucarotti, B.F. Koop, and D.B. Levin (2006). Sequence Analysis and Organization of the Neodiprion abietis Nucleopolyphedrovirus Genome. Journal of Virology. 80(14): 6952-6960.
  11. L.J. Anstey, D.T. Quiring, D.P. Ostaff (2002). Seasonal Changes in Intra-tree Distribution of Immature Balsam Fir Sawfly (Hymenoptera: Diprionidae). Canadian Entomologist. 134: 529-538.
  12. G. Rogers, D.T. Quiring, and C.J. Lucarotti (2012). Transmission of a Gammabaculovirus within Cohorts of Balsam Fir Sawfly (Neodiprion abietis) Larvae. Journal of Insects. 3(4): 989-1000.
  13. 1 2 G. Moreau (2006). Past and present outbreaks of the balsam fir sawfly in western Newfoundland: An analytical review. Forest Ecology and Management 221: 215-219.
  14. 1 2 G. Moreau, D.P. Ostaff, É. Bauce, E.S. Eveleigh, C.J. Lucarotti, B. Morin, and D.T. Quiring (2018) Interlacing roles of bottom-up, top-down, endogenous and anthropogenic factors in population oscillations. Ecosphere 9: e02421.
  15. 1 2 3 G. Moreau (2004). The influence of forest management on defoliator populations: a case study with Neodiprion abietis in precommercially thinned and natural forest stands. PhD dissertation, University of New Brunswick, Fredericton, New Brunswick, Canada.
  16. 1 2 G. Moreau, E.S. Eveleigh, C.J. Lucarotti, and D.T. Quiring (2006). Ecosystem Alteration Modifies the Relative Strengths of Bottom-up and Top-down Forces in a Herbivore Population. Journal of Animal Ecology. 75: 853–861.
  17. G. Moreau, E.S. Eveleigh, C.J. Lucarotti, B. Morin, D.T. Quiring (2017) Opposing effects of mortality factors on progeny operational sex ratio may thwart adaptive manipulation of primary sex ratio. Ecology and Evolution 7(13): 4973–4981.
  18. 1 2 H.D. Piene, D. Ostaff, E.S. Eveleigh (2001). Growth loss and recovery following defoliation by the balsam fir sawfly in young, spaced balsam fir stands. The Canadian Entomologist 133:675–686.
  19. 1 2 D.P. Ostaff, H. Piene, D.T. Quiring, G. Moreau, J.C.G. Farrell, T. Scarr (2006). Influence of pre-commercial thinning of balsam fir on defoliation by the balsam fir sawfly. Forest Ecology and Management 223:342–348.
  20. G. Moreau, E.S. Eveleigh, C.J. Lucarotti, D.T. Quiring (2006). Stage-specific responses to ecosystem alteration in an eruptive herbivorous insect. Journal of Applied Ecology 43: 28-34.
  21. G. Moreau, D.T. Quiring (2011). Stand structure interacts with previous defoliation to influence herbivore fitness. Forest Ecology and Management 262: 1567-1575.
  22. G. Moreau, C.J. Lucarotti, E.G. Kettela, G.S. Thurston, S. Holmes, C. Weaver, D.B. Levin, B. Morin (2005). Aerial application of nucleopolyhedrovirus induces decline in increasing and peaking populations of Neodiprion abietis. Biological control 33: 65-73.
  23. G. Moreau, C.J. Lucarotti (2007). A brief review of the past use of baculoviruses for the management of eruptive forest defoliators and recent developments on a sawfly virus in Canada. The Forestry Chronicle 83: 105-112.
  24. C.J. Lucarotti, H.W.W Beatrixe, R. Lapointe, B. Morin, D.B. Levin (2012). Pathology of a Gammabaculovirus in Its Natural Balsam Fir Sawfly (Neodiprion abietis) Host. Journal of Entomology. 2012: 1-13.
  25. S.Y. Li, A.C. Skinner, T. Rideout, M.D. Stone, H. Crummey, and G. Holloway (2003). Lethal and Sublethal Effects of a Neem-based Insecticide on Balsam Fir Sawfly (Hymenoptera: Diprionidae). Journal of Economic Entomology. 96(1): 35-42.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.