Diprion similis

(Hartig, 1834)

Introduced Pine Sawfly, Imported Pine Sawfly, White Pine Sawfly

Diprion similis is a conifer-feeding to central and northern Europe and Asia that has become in North America following its accidental introduction around 1914. The is notable for its , where unfertilized develop into male offspring, facilitating rapid establishment. are gregarious defoliators of pine needles, with a strong preference for pine (Pinus strobus) in North America. The species exhibits two per year in many regions, with second-generation larvae as in . Its invasive success has been attributed to parthenogenetic capabilities, lack of in ranges, and specialized communication involving the (2S,3R,7R)-propionate isomer of 3,7-dimethylpentadecan-2-ol.

Diprion similis by (c) Ken-ichi Ueda, some rights reserved (CC BY). Used under a CC-BY license.Diprion similis by (c) Ken-ichi Ueda, some rights reserved (CC BY). Used under a CC-BY license.Diprion similis by (c) Ken-ichi Ueda, some rights reserved (CC BY). Used under a CC-BY license.

Pronunciation

How to pronounce Diprion similis: /dɪˈpraɪ.ɒn ˈsɪmɪ.lɪs/

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Identification

distinguished from other by structure ( in males, in females) and color pattern. The can be separated from the North Neodiprion pinetum (also called ' pine ') by chemistry: D. similis uses the (2S,3R,7R)-propionate isomer, while N. pinetum uses the (2S,3S,7S)-acetate isomer. identified by black capsule, gregarious feeding , and characteristic longitudinal striping in later ; the larval in Davis et al. (2023) provides field identification tools.

Images

Appearance

males measure 7–9 mm in length, entirely black with legs except for brownish-black and femoral bases; are black and (feather-like). Adult females are slightly larger at 7.5–10 mm, with black and and variable abdominal coloration ranging from yellow and black to entirely dark; antennae are black and (saw-like). possess black heads and -like bodies: early are yellowish-green, while later instars develop black longitudinal stripes with yellow and on a bluish-black background. Females have six larval instars, males have five.

Habitat

Coniferous forests and plantations, particularly those containing Pinus strobus ( pine). In North America, occurs in mature white pine plantations and forest edges. range includes and temperate pine forests of Europe and Asia.

Distribution

to central and northern Europe (including Fennoscandia), Russian Siberia (to Lake Baikal), and China. to North America: first detected in Connecticut in 1914, now established throughout eastern United States and Canada wherever Pinus strobus occurs.

Seasonality

Two per year in most of range. emerge in spring and remain active through summer; peak male in early June in Ontario. First-generation present in early summer, with formed in July and adult in August. Second-generation larvae appear in late summer, overwinter as in cocoons from autumn through spring, with some individuals entering extended lasting up to three years.

Diet

feed exclusively on pine needles (). In range: Pinus sylvestris, P. mugo, P. cembra, P. sibirica, and P. strobus and P. contorta. In North America: primarily Pinus strobus, also P. resinosa, P. banksiana, and P. sylvestris. Young larvae feed on needle edges, consuming partial tissue; older larvae consume entire needles.

Host Associations

  • Pinus strobus - primary Strong preference in North America; traps baited with placed in pine plantations
  • Pinus sylvestris - range and secondary host in North America
  • Pinus resinosa - North
  • Pinus banksiana - North
  • Pinus mugo - range
  • Pinus cembra - range
  • Pinus sibirica - range
  • Pinus contorta - in range

Life Cycle

with two annually. laid in slits cut into pine needles by female's saw-like , approximately 10 eggs per needle. through five (males) or six (females) , with early instars gregarious and later instars solitary. First-generation larvae pupate in silken on tree, emerging as in approximately one month. Second-generation larvae descend to ground, spin cocoons, and overwinter as ; occurs in spring. Some individuals remain in extended prepupal for up to three years. Adults are short-lived and do not feed.

Behavior

Newly hatched exhibit gregarious feeding, forming groups on foliage; later become solitary. Larvae are feeders. employ -mediated mate location: females release (propanoate ester of (2S,3R,7R)-3,7-dimethylpentadecan-2-ol) to attract males. Unmated females can produce viable male offspring through . Males are attracted to synthetic pheromone lures in field trapping; threo four-isomer blends are equally attractive as pure main component at matched release rates.

Ecological Role

function as and defoliators of pine . In range, are regulated by including and . In North range, populations have expanded with limited top-down control, leading to localized capable of reducing tree growth rates and causing mortality. Serves as for birds and supports parasitoid where established.

Human Relevance

Significant forest pest in North America, particularly in pine plantations and ornamental plantings. Economic impacts include reduced timber growth, tree mortality, and costs of and management. -based monitoring systems have been developed using the identified (2S,3R,7R)-propionate compound. Management options include manual removal of , high-pressure water sprays for small , and targeted for large ; is generally preferred.

Similar Taxa

  • Neodiprion pinetumAlso feeds on pine and shares 'white pine '; distinguished by chemistry (uses (2S,3S,7S)-acetate isomer), to North America, and different larval coloration patterns
  • Diprion piniEuropean with overlapping range; uses different component (propanoate of 3,7-dimethyltridecan-2-ol) that is not attractive to D. similis males
  • Dermacentor similisUnrelated described from western North America that shares the same specific epithet; no biological relationship but potential for nomenclatural confusion

Misconceptions

The ' pine ' is ambiguous and confusing because it is applied to both D. similis (, ) and Neodiprion pinetum ( North ). The two species are not closely related and differ in chemistry, distribution, and management needs.

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Sources and further reading