Forbe's Tree Cricket - Oecanthus forbesi
Preface to the Genus Oecanthus
The following is taken from Fulton (1915, June 1926), Walker (1962), and Funk (1982). Species in this genus are divided into 4 natural groups based on their morphology, color and habits. These groups are niveus
, and varicornis
. Only two groups occur in Montana, with 4 species in the nigricornus
group and one species, Snowy Tree Cricket
), in the releyi
Generally, tree crickets are characterized by their long, slender shape, pale colors and arboreal habits. The tegmina (forewings) of males are broad and flat, and female wings are long and narrow and wrapped closely to the body. Their legs are very slender, armed with two rows of minute teeth interspersed with a number of delicate spines. The tarsi (feet) are three-segmented with the second segment being small and compressed. The antennae are longer than the body, filiform and often ornamented with distinctive black markings. The first two basal antennal segments are distinctively marked with spots, which are a convenient diagnostic character for species identification (see illustrations for each species).
The following is from Fulton (1915, June and October 1926), Hebard (1928), Walker (1963), Helfer (1971), Capinera and Sechrist (1982), Vickery and Kevan (1985), Bland (2003), Capinera et al. (2004), Himmelman (2009), Scott (2010), and Walker (2020 Singing Insects of North America
). Both O. forbesi
and Black-horned Tree Cricket
) are morphologically indistinguishable and separable only by their songs. The wings (tegmina) are yellow-green and translucent and the abdomen has blackish segments that can be seen through it. The head, pronotum, antennae and legs are black. However, the degree of blackness can be quite variable, with some specimens bearing only black stripes on the head, pronotum and abdomen. Specimens in the eastern portion of their geographical range tend to be darker than those occupying the western range, although the distal end of the hind femurs and legs are generally always black.Song production in Oecanthus
Song is produced only by males, which raise their forewings (tegmina) perpendicular to the body and vibrate them in a transverse direction, so that the overlapping inner portions rub against each other. The sound-producing mechanism is located near the base of the wings. It is a broad expanded distal area which serves as a resonator to increase sound volume. A short prominent transverse vein occurs beneath forming a rasp-like structure about 1-1.5 mm wide with 20-50+ short teeth, depending upon the species, inclined toward the opposite wing. The number of teeth is a diagnostic feature. The right wing, termed the file, bears a series of downward projecting teeth, overlaps the left, termed the scraper. When the tegmina are raised and alternately opened and closed, the song is produced only on the closing stroke. Due to this partial wing-motion cycle, cricket songs are constructed of sound pulses. If a cricket opens and closes its wings many times in succession, it produces a trill. If the wings are opened and closed a few times, pauses, and repeats the song again, it produces a chirp. Songs vary according to ambient temperatures and is distinctive by sound analysis between species.
The song of the Forbe's and Black-horned Tree Cricket
has been described as a rich, high continuous trill heard both day and night and also similar to that of the Four-spotted Tree Cricket
). Therefore, it is recommended that one refer to the sonograms and recordings in Elliott and Hershberger’s The Songs of Insects
(2007), Himmelman's Guide to Night-Singing Insects of the Northeast
(2009), and Walker’s SINA website (2020).
This species overwinters in the egg stage. Nymphs appear in late June to early July. Adults occur through most of August and September with some persisting into October or the first autumn frost (Vickery and Kevan 1985).
The following comes from Fulton (1915, June and October 1926), Hebard (1928), Walker (1963), Helfer (1971), Capinera and Sechrist (1982), Vickery and Kevan (1985), Bland (2003), Capinera et al. (2004), Himmelman (2009), and Scott (2010). The body length for males and females is 13-19 mm. Length of the stridulatory file is >1 mm, possessing 37-71 teeth with an average of ±44. The first basal antennal segment has two paired black spots that are sometimes connected and/or obscured by black speckling. The second segment has two vertical spots and likewise can be connected and/or obscured by speckling (see illustration).
species are similar in general form, appearance and behavior as noted above. The Forbe's and Black-horned Tree Crickets
have similar looking, thick markings on the 1st and 2nd antennal segments. Separation of the two species from the Prairie Tree Cricket
) is by song. Both the Forbe's and Black-horned Tree Crickets
song is faster.
Oecanthus forbesi has a similar, overlapping, distribution to that of Oecanthus nigricornis but only extends eastward to Michigan and the western half of Ohio. Its occurrence in Montana counties is uncertain due to the morphological similarity of the two species and lack of acoustical data (Vickery and Kevan 1985, Scott 2010, and Walker 2020).
Observations in Montana Natural Heritage Program Database
Number of Observations:
(Click on the following maps and charts to see full sized version)
Map Help and Descriptions
(Observations spanning multiple months or years are excluded from time charts)
The Black-horned Tree Cricket
, (O. nigrocornis
), and Forbe's Tree Cricket, (O. forbesi
), prefer similar habitats with larger plants and more dense growth than that preferred by the similarly associated Four-spotted Tree Cricket
). Both inhabit tall, rank growth of weeds, woody brush, vines and small trees such as willows (Salix
sp.), sumac (Rhus
sp.), and are commonly associated with goldenrod (Solidago
sp.) and blackberry (Rubus
sp.), usually in fencerows, as well as wetlands and river bottoms. They are not commonly found in dry, sparsely vegetated fields nor in the crowns of tall trees, and generally stay about one meter above the ground, with the Forbe's Tree Cricket occupying niches less than a meter closer to the ground (Fulton 1915, Vickery and Kevan 1985, and Walker 1963).
The food habits of all the Oecanthus species consists of a great variety of both plant and animal origin, but the food items must be soft enough to be masticated by their weak jaws. One of their dietary mainstays is aphids. They also consume plant material by chewing holes in leaves, outer tissue of stems, the anthers of some plant flowers, chew holes in ripe fruit (apples, peaches, plums, etc.) to feed on the inner pulp, and eat fruiting bodies of fungi (Fulton June 1926, Vickery and Kevan 1985, and Himmelman 2009).
Reproduction in Oecanthus
The following is taken from Fulton (1915, June 1926), Walker (1962), and Funk (1982). The mating and reproduction habits of all Oecanthus
species are generally similar in behavior and complexity. When a female is attracted to a singing male, she approaches him from the rear because that is direction most of the sound travels and amplified by his wings. When the male senses the female’s approach, he stops singing, turns around and touches her with his antennae. It is thought that this “tasting” of her confirms she is the same species and an appropriate mate. The next step in the courtship ritual, (can vary slightly among species) the male again sings and rocks from side to side or pounds his abdomen on the substrate. If the female is receptive to his “romantic overtures,” she climbs onto his back, the male raises his tegmina at a 45° angle, and she begins feeding on a substance secreted from a glandular cavity, called the metanotal, metathoracic or Hancock’s gland (which he called the “alluring gland”) located between the wing bases. The secretions empty into a pit at the base of the male’s hind wings where they are accessible to the female once she is in the copulatory position. After she begins to feed, she allows the male to mate with her. During copulation, the male reaches his abdomen back, the female bends her abdomen downward connecting their genitalia, and the male passes a sperm-containing spermatophore to the female. The spermatophore is ovoid and possesses a thin, threadlike tube which enters the female, leaving the spermatophore to dangle outside her genital opening and, when internally attached, sperm begins to move through the tube. After copulation, the female always eats the spermatophore because it is thought to contain nutrients which may enhance egg production. The female remains astride the male for 5-20 minutes or more, continuing to feed from the metanotal gland. When she stops feeding, she dismounts, but the male may attempt to resume active courtship by repeatedly backing under the female until she either remounts or moves away. If remounting occurs, the renewed courtship may require another 20 minutes or more. Such resumed courtship and mating is thought to ensure that large numbers of sperm pass from his spermatophore into the female’s sperm-storage organ called the spermatheca. When the female is ready to lay eggs, sperm are released from the spermatheca and fertilize the eggs as they pass down the oviduct. The female selects a suitable egg-laying site on a woody or herbaceous plant to oviposit and chews a small hole in the stem, then moves forward slightly, arches her back, bringing her ovipositor perpendicular to the hole moving it up and down drilling the hole with thrusts and turning it around by twisting her abdomen. The drilling time may require 5-25 minutes, depending upon the plant’s wood or fiber density. Once the hole is drilled to the proper size and depth, the female moves an egg down her ovipositor, fills the hole with a mucilaginous substance, removes the ovipositor, and neatly caps the hole with chewed plant material. The entire process from chewing the bark to sealing the hole may take a quarter hour to nearly a full hour.
Preferred plant species for oviposition are wide, including Raspberry/Blackberry (Rhus
sp.), Fleabanes/Asters (Erigeron
sp.), Goldenrods (Solidago
sp.), box elder
), sumac (Rhus
sp.), grape (Vitis
sp.), willow (Salix
sp.), elm (Ulmus
sp.) and also orchard trees like peach, apple and cherry. Both the Forbe's and the Black-horned Tree Cricket
select larger stems for egg-laying, measuring 5 mm up to about 1 centimeter in diameter. Oviposition begins in late August through September. Upon hatching, the two species pass through 5 instars before reaching the adult stage (Fulton 1915, and Vickery and Kevan 1985).
- Literature Cited AboveLegend: View Online Publication
- Bland, R.G. 2003. The Orthoptera of Michigan—Biology, Keys, and Descriptions of Grasshoppers, Katydids, and Crickets. East Lansing, MI: Michigan State University Extension, Bulletin E-2815. 221 p.
- Capinera, J.L. and T.S. Sechrist. 1982. Grasshoppers of Colorado: Identification, Biology, and Management. Fort Collins, CO: Colorado State University Experiment Station, Bulletin 584S. 161 p.
- Capinera, J.L., R.D. Scott, and T.J. Walker. 2004. Field Guide to Grasshoppers, Katydids, and Crickets of the United States. Ithaca, NY. Cornell University Press.
- Elliott, L. and W. Hershberger. 2007. The songs of insects. New York, NY: Houghton Mifflin Harcourt. 227 p.
- Fulton, B.B. 1915. The tree crickets of New York: life history and bionomics. New York Agricultural Experiment Station Technical Bulletin 42.
- Fulton, B.B. June 1926. The tree crickets of Oregon. Oregon Agricultural College Experiment Station, Station Bulletin 223. 20 p.
- Fulton, B.B. October 1926. Geographical variation in the Nigrocornis group of Oecanthus (Orthoptera). Iowa State College Journal of Science 1(1):42-46.
- Funk, D.H. 1982. The mating of tree crickets. Scientific American 261(2):50-59.
- Hebard, M. 1928. The Orthoptera of Montana. Proceedings of the Academy of Natural Sciences of Philadelphia, Vol. 80:211-306.
- Helfer, J.R. 1971. How to Know the Grasshoppers, Crickets, Cockroaches, and Their Allies. Revised edition (out of print), Mineola, NY: Dover Publications.
- Himmelman, J. 2009. Guide to Night-Singing Insects of the Northeast. Mechanicsburg, PA: Stackpole Books. 160 p.
- Scott, R.D. 2010. Montana Grasshoppers, Katydids, and Crickets A Pictorial Field Guide to the Orthoptera. MagpieMTGraphics, Billings, MT.
- Vickery, V. R. and D. K. M. Kevan. 1985. The grasshopper, crickets, and related insects of Canada and adjacent regions. Biosystematics Research Institute, Ottawa, Ontario. Publication Number 1777. 918 pp.
- Walker T.J.(ed.). 2020. Singing insects of North America. Accessed 10 February 2021. https://orthsoc.org/sina/
- Additional ReferencesLegend: View Online Publication
Do you know of a citation we're missing?
- Alexander, R.D. and D. Otte. 1967. The evolution of genitalia and mating behavior in crickets (Gryllidae) and other Orthoptera. Ann Arbor, MI: University of Michigan. Misc. publications, Museum of Zoology, No. 133. 69 p.
- Brown, W.D. 1997. Courtship feeding in tree crickets increases insemination and reproductive life span. Animal Behavior 54:1369-1382.
- Dethier, V.G. 1992. Crickets and Katydids, Concerts and Solos. Cambridge, MA: Harvard University Press. 140 p.
- Gangwere, S.K., M.C. Muralirangan, and M. Muralirangan (eds). 1997. The bionomics of grasshoppers, katydids and their kin. New York, NY: CAB International. 528 p.
- Himmelman, J. 2011. Cricket radio: tuning in the night-singing insects. Cambridge, MA: The Belknap Press of Harvard University Press. 272 p.
- Walker, T.J. 1963. The taxonomy and calling songs of United States tree crickets (Orthopters:Gryllidae:Oecanthus). The nigricornis group of the genus Oecanthus. Annals of the Entomological Society of America 56(6):772-789.
- Walker, T.J. 1967. The metanotal gland as a taxonomic character in Oecanthus of the United States. Proceedings of the Entomological Society of Washington 69(2):151-167.
- Walker, T.J. 1969. Acoustic synchrony: two mechanisms in the snowy tree cricket. Science 166:891-894.
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