Ophiogomphus howei

Ge­o­graphic Range

Ophio­gom­phus howei, com­monly known as the pygmy snake­tail drag­on­fly, is a na­tive species to North Amer­ica. Pygmy snake­tail drag­on­flies are found on the east­ern half of North Amer­ica in two dis­tinct lo­ca­tions; one pop­u­la­tion which fol­lows along the Ap­palachian re­gion ex­tend­ing from Ten­nessee to New Brunswick, On­tario, and the west­ern pop­u­la­tions in Michi­gan, Min­nesota, and Wis­con­sin. The pygmy snake­tail drag­on­fly can be found in ten known U.S. states: Ken­tucky, Maine, Mass­a­chu­setts, Michi­gan, Min­nesota, New York, North Car­olina, Penn­syl­va­nia, Ten­nessee, and Wis­con­sin. Ophio­gom­phus howei can be found in the Cana­dian ter­ri­to­ries of On­tario and Que­bec in var­i­ous lo­ca­tions. Much of north­west­ern On­tario and the west­ern United States are with­out suit­able habi­tat due to the lim­i­ta­tions as­so­ci­ated with this species which in­cludes large, clear, fast-mov­ing rivers with fine gravel sub­strate. (Ab­bott and Don­nelly, 2013; Brunelle, 2008; Hamill, 2013)

Habi­tat

Lar­vae of the pygmy snake­tail drag­on­fly are found in large rivers with clear, fast-flow­ing, and un­pol­luted run­ning wa­ters and sub­strates of fine sand or pea sized gravel. The medium to large sized rivers range from 10 me­ters to 200 me­ters wide with fine sub­strate stream beds. Lar­vae do not occur in areas below dams, since the species is un­able to breed at such deep depths. They are typ­i­cally found at depths of 1 to 4 m.

The ma­jor­ity of adult life for Ophio­gom­phus howei species is spent hid­den in forests along large rivers, which makes this species par­tic­u­larly dif­fi­cult to study. The for­est sur­round­ing the river is needed, par­tic­u­larly for fe­males, to pro­vide habi­tat for for­ag­ing and mat­ing. The spe­cific type of for­est re­quired has not been de­scribed in pub­li­ca­tions, but is most likely a mix­ture of de­cid­u­ous and conif­er­ous for­est. (Ab­bott and Don­nelly, 2013; Brunelle, 2008; Hamill, 2013)

  • Aquatic Biomes
  • lakes and ponds
  • rivers and streams
  • Range depth
    1 to 4 m
    3.28 to 13.12 ft

Phys­i­cal De­scrip­tion

Sim­i­lar to other drag­on­fly species, lar­vae of pygmy snake­tail drag­on­fly are flat, brown, and have di­ver­gent wing cases. Lar­vae can eas­ily be iden­ti­fied from other mem­bers of the genus Ophio­gom­phus by their small size (19 to 22 mm in length), by their lack of dor­sal ab­dom­i­nal spines, and ab­sence of lat­eral hooks on the ab­dom­i­nal seg­ment 7. The ab­dom­i­nal re­gion also shows long cerci, which are a pair of upper ap­pendages at the tip of seg­ment 10 at the end of the ab­domen.

The ma­ture nymph of Ophio­gom­phus howei is green­ish brown in color with a body cov­ered with coarse gran­ules to help it blend into the river bot­tom. Ear­lier in­stars have more of a yel­low­ish-brown body. The body length is on av­er­age 20.5 mm, ab­dom­i­nal width 5.6 mm, and head width 4.7 mm.

The adults of Ophio­gom­phus howei are the small­est (31 to 37 mm long) mem­bers of the Ophio­gom­phus genus as the com­mon name of "pygmy snake­tail drag­on­fly" im­plies, and is one of the smaller drag­on­flies in North Amer­ica with a hind-wing length of 19 to 21 mm and ab­domen length of 22 to 24 mm. The adults have dis­tinc­tive mark­ings and col­oration show­ing a bright green tho­rax, vivid yel­low mark­ings on the dor­sal ab­domen, and each wing is marked basally with a large, trans­par­ent yel­low-or­ange patch. In the ten­eral stage, the tho­racic mark­ings are yel­low for up to seven days.

Com­pared to other drag­on­flies of this genus the pygmy snake­tail drag­on­fly has a greater flared ab­domen. The fe­male re­sem­bles the male ex­cept for its thicker ab­domen, re­duced flare, lack of sec­ondary gen­i­talia, pres­ence of an ovipos­i­tor, and dif­fer­ent num­ber and shape of the ab­dom­i­nal ap­pendages. The inner or basal por­tions of the hind-wings are yel­low (basal half of the hind-wings in males, basal two-thirds of the hind-wings in fe­males). The ab­domen is de­scribed as hav­ing a "club­tail" since it is slightly widened at the end.

The ab­domen is black in color with small, yel­low spots on top that are tri­an­gu­lar in shape and of var­i­ous sizes. All ab­dom­i­nal seg­ments have a yel­low, tri­an­gu­lar spot on top ex­cept for the last seg­ment at the pos­te­rior end of the ab­domen (seg­ment 10). The eyes of this drag­on­fly are sim­i­lar to other drag­on­fly species, col­ored green and do not meet at the top of the head. Fe­males can be dis­tin­guished from males be­cause they have a short, sharp horn on each side of the rear of the head. (Brunelle, 2008; Hamill, 2013; Kennedy and White III, 1979; Lee, 2009; "Ophio­gom­phus howei - Brom­ley, 1924", 2013; Ten­nessen, 1993)

  • Sexual Dimorphism
  • sexes colored or patterned differently
  • sexes shaped differently
  • Range length
    31 to 37 mm
    1.22 to 1.46 in
  • Range wingspan
    19 to 21 mm
    0.75 to 0.83 in

De­vel­op­ment

Ophio­gom­phus howei ex­hibits hemimetabolous meta­mor­pho­sis, mean­ing a grad­ual de­vel­op­ment with three dis­tinct stages that some­what re­sem­ble one an­other and lacks a pupal stage. Stages for the life cycle in­cludes an aquatic egg, aquatic larva, and a ter­res­trial/aer­ial adult. As with most drag­on­flies, the pygmy snake­tail spends most of its life as an aquatic larva. After the eggs hatch, the lar­vae bur­row into gravel or sand sub­strates where they grow and de­velop. As the lar­vae grow, they shed or molt their skin nu­mer­ous times. Most drag­on­fly species trans­form into adults in one to three years. A few stud­ies have in­di­cated the pygmy snake­tail drag­on­fly may have a two-year life cycle.

At the end of their lar­val de­vel­op­ment, the lar­vae climb out of the water and at­tach them­selves to veg­e­ta­tion, rocks, tree roots, woody de­bris, bare ground, or other struc­tures or sur­faces lo­cated along the stream banks or float­ing in the water as they trans­form into the adult stage. The lar­vae un­dergo a final molt and emerge as winged adults. Newly emerged adults, or ten­er­als, typ­i­cally re­main perched for one or two hours to dry their wings be­fore they can fly. Adult drag­on­flies be­come sex­u­ally ma­ture within a week or up to a month after emer­gence. (Bradeen and Boland, 2004; Lee, 2009; "The Uni­ver­sity of Ari­zona Cen­ter for In­sect Sci­ence Ed­u­ca­tion Out­reach", 1997)

Re­pro­duc­tion

Adult pygmy snake­tail drag­on­flies be­come sex­u­ally ma­ture usu­ally within a week or up to a month after emer­gence. Males will ini­ti­ate mat­ing by grasp­ing fe­males with their legs and ter­mi­nal ap­pendages, then the con­nected pairs fly in tan­dem to nearby veg­e­ta­tion or tree canopies to mate. Breed­ing oc­curs sea­son­ally usu­ally dur­ing spring or early sum­mer. Most likely pygmy snake­tail drag­on­flies are polyg­y­nan­drous, with both males and fe­males hav­ing mul­ti­ple mates. (Lee, 2009; "Ophio­gom­phus howei - Brom­ley, 1924", 2013)

After mat­ing, fe­males lay their eggs in rif­fles or rapids in streams and rivers by dip­ping their ab­domen in the mov­ing water. The eggs are car­ried by the water and are de­posited in spaces in the rock, gravel, and/or sand sub­strate of the stream or river. Adult pygmy snake­tail drag­on­flies are ob­served oc­ca­sion­ally at breed­ing sites, but gen­er­ally are not seen as fre­quently or in large num­bers after the adult emer­gence pe­riod com­pared to other drag­on­fly species. This issue leads to a lack of cur­rent in­for­ma­tion on the num­ber of off­spring pro­duced per breed­ing sea­son and other re­pro­duc­tive in­for­ma­tion. Stud­ies like the one by Gibbs et. al. (2004) in­di­cates that the pygmy snake­tail drag­on­fly likely re­quires two or more years to com­plete a gen­er­a­tion. It also likely has over­lap­ping gen­er­a­tions and pro­duces more than one brood or gen­er­a­tion per year. (Bradeen and Boland, 2004; Lee, 2009)

  • Breeding interval
    Ophiogompus howei mates multiple times during its breeding season.
  • Breeding season
    Breeding takes place in the spring or early summer.
  • Average time to independence
    0 minutes
  • Range age at sexual or reproductive maturity (female)
    1 to 3 weeks
  • Range age at sexual or reproductive maturity (male)
    1 to 3 weeks

Fe­male pygmy snake­tail drag­on­flies lay their eggs in suit­able aquatic habi­tats for the lar­vae to sur­vive in upon hatch­ing. They also pro­vide pro­vi­sion­ing in the eggs. After lay­ing her eggs, the fe­male drag­on­fly then leaves the area and the eggs are car­ried away by the water. Males are only used in fer­til­iza­tion and have no role in parental in­vest­ment. (Lee, 2009; "Ophio­gom­phus howei - Brom­ley, 1924", 2013)

  • Parental Investment
  • pre-hatching/birth
    • provisioning
      • female

Lifes­pan/Longevity

As with most drag­on­flies, the Ophio­gom­phus howei spends most of its life as an aquatic larva. The over­all lifes­pan for O. howei is de­pen­dent on lar­val and nymph stages which is highly vari­able due to vul­ner­a­bil­ity to birds, frogs, lizards, fish, and other large drag­on­flies, weather, and pol­lu­tion. The time re­quired for pygmy snake­tail lar­vae to de­velop into adults is cur­rently not known. Most drag­on­fly species trans­form into adults in one to three years. In gen­eral, adult drag­on­flies typ­i­cally live for ap­prox­i­mately one month, and up to nine months to a year in a few species. (Lee, 2009)

  • Average lifespan
    Status: wild
    2 years

Be­hav­ior

Adult drag­on­flies need sunny warm weather to fly, with a tem­per­a­ture over 65°C ideal. Dur­ing in­clement weather such as cold and rainy days, O. howei tends to hide or lay in veg­e­ta­tion. Adult male drag­on­flies often es­tab­lish ter­ri­to­ries along the edges of ponds or streams and only de­fend the ter­ri­tory against other males of their species. The lar­val and nymph stages of Ophio­gom­phus howei are mainly soli­tary within a river or stream, but they may travel within the river or stream over the span of the species life. (Ham­mond, 2014)

Home Range

Since the pygmy snake­tail drag­on­fly spends most of its ex­pected life within a river, the home range of typ­i­cal species could ex­tend from about 1300 km or (ap­prox 800 miles) over the span of a river. Most of the adult life of the drag­on­fly is spent in close veg­e­ta­tion or trees about (7 to 10 me­ters) off the ground di­rectly next to the river, and may mi­grate along the length of the river or stream. (Kennedy and White III, 1979; Ten­nessen, 1993)

Com­mu­ni­ca­tion and Per­cep­tion

Adult pygmy snake­tail drag­on­flies are sim­i­lar to other drag­on­fly species who com­mu­ni­cate vi­su­ally. Mat­ing pairs prob­a­bly com­mu­ni­cate by touch, shown when an adult male grasps fe­males with their legs and ter­mi­nal ap­pendages and its pos­si­ble that chem­i­cal com­mu­ni­ca­tion may play a role in re­pro­duc­tion as well. Adult males also fight aer­ial duels for ter­ri­to­ries, dis­play­ing their size and speed to each other in order to com­mu­ni­cate and ward off other drag­on­fly species. (Ham­mond, 2014; Har­ris, et al., 2011; Lee, 2009)

Food Habits

Both adult and lar­val pygmy snake­tail drag­on­flies are known as in­tensely fe­ro­cious car­ni­vores and preda­tors of most in­sect species. Pygmy snake­tails have great speed in both the air and water, which al­lows them to sneak and cap­ture prey. Lar­vae have been re­ported to feed on water mites, mayfly nymphs, and chi­rono­mids or midges as they hide be­hind rocks, gravel, sticks, and other de­bris from which they at­tack un­sus­pect­ingly. Adult drag­on­flies typ­i­cally for­age for fly­ing in­sects, such as but­ter­flies, moths, dam­selflies, mos­qui­toes, and flies, in sunny areas in­clud­ing open grassy fields, for­est open­ings, and over streams and rivers. (Kennedy and White III, 1979; Lee, 2009)

  • Animal Foods
  • insects
  • terrestrial non-insect arthropods
  • aquatic or marine worms

Pre­da­tion

Preda­tors of adult drag­on­flies in­clude birds, frogs, lizards, fish, and other large drag­on­flies. When the drag­on­fly has use of its wings, it is quick and agile in flight, and hides in veg­e­ta­tion when it is too cold to fly. The O. howei species has adapted bright mark­ings and a "club­tail" which most likely serves to warn off preda­tors. Adult pygmy snake­tail drag­on­flies also have high mor­tal­ity rates due to human dis­tur­bance or en­vi­ron­men­tal fac­tors such as wind/rain after the ini­tial hatch­ing time when the wings of the drag­on­fly are wet for one or two hours. The col­oration of lar­vae likely serves as cam­ou­flage in its aquatic habi­tat. (Ham­mond, 2014; Lee, 2009)

  • Anti-predator Adaptations
  • cryptic

Ecosys­tem Roles

Pygmy snake­tail drag­on­flies are an im­por­tant species in their habi­tats. The preda­tors of pygmy snake­tail drag­on­flies such as birds, frogs, lizards, fish, and other large drag­on­flies all con­sume this species and pygmy snake­tails con­sume water mites, mayfly nymphs, chi­rono­mids or midges, but­ter­flies, moths, dam­selflies, mos­qui­toes, and flies. With­out the pygmy snake­tail many species within the food web would be af­fected. An­other im­por­tant role Ophio­gom­phus howei pro­vides is soil aer­a­tion. The lar­vae hide in be­tween rocks and gravel and tends to move small gran­u­lar sized sand grains at the bot­tom of streams and rivers, which serves to break up soil and al­lows water and air to enter the open cav­ity. (Lee, 2009)

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

Pygmy snake­tail drag­on­flies are eco­nom­i­cally im­por­tant for hu­mans as they help to con­trol pop­u­la­tions of mos­qui­toes. Ophio­gom­phus howei has also pro­vided ample op­por­tu­ni­ties for re­search, in­clud­ing such top­ics as re­pro­duc­tive ac­tiv­i­ties and tim­ing, ef­fects of in­va­sive species, food pref­er­ences and for­est habi­tat needs of adults, re­col­o­niza­tion abil­i­ties of the species after ex­tir­pa­tion, po­ten­tial for and fea­si­bil­ity of rein­tro­duc­tion after ex­tir­pa­tion. (Hamill, 2013)

  • Positive Impacts
  • research and education
  • controls pest population

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

There are no known ad­verse ef­fects of Ophio­gom­phus howei on hu­mans.

Con­ser­va­tion Sta­tus

Threats to the ma­jor­ity of the pygmy snake­tail drag­on­fly in the north­ern range are mod­er­ate, but habi­tat threats to pop­u­la­tions in the south ap­pear to be more sig­nif­i­cant. These po­ten­tial threats to habi­tat degra­da­tion can ac­count from human ac­tiv­i­ties that ruin run­ning wa­ters through poorly drained roads, damming, and also nat­ural ac­tiv­i­ties such as beaver damming, chan­nel­iza­tion lead­ing to scour of mi­cro­hab­i­tats, toxic or or­ganic pol­lu­tion, and in­tro­duc­tions of ex­otic species. The ma­jor­ity of re­pro­duc­tion which in­cludes mi­gra­tion is ef­fected by cli­mate and weather and will be po­ten­tially im­pacted with rapid cli­mate changes. (Ab­bott and Don­nelly, 2013)

Con­trib­u­tors

Brock Bermel (au­thor), Min­nesota State Uni­ver­sity, Mankato, Robert Sorensen (ed­i­tor), Min­nesota State Uni­ver­sity, Mankato, An­gela Miner (ed­i­tor), An­i­mal Di­ver­sity Web Staff.

Glossary

Nearctic

living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.

World Map

arboreal

Referring to an animal that lives in trees; tree-climbing.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

carnivore

an animal that mainly eats meat

chemical

uses smells or other chemicals to communicate

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.

diurnal
  1. active during the day, 2. lasting for one day.
ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

fertilization

union of egg and spermatozoan

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

freshwater

mainly lives in water that is not salty.

heterothermic

having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.

insectivore

An animal that eats mainly insects or spiders.

internal fertilization

fertilization takes place within the female's body

iteroparous

offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).

metamorphosis

A large change in the shape or structure of an animal that happens as the animal grows. In insects, "incomplete metamorphosis" is when young animals are similar to adults and change gradually into the adult form, and "complete metamorphosis" is when there is a profound change between larval and adult forms. Butterflies have complete metamorphosis, grasshoppers have incomplete metamorphosis.

motile

having the capacity to move from one place to another.

natatorial

specialized for swimming

native range

the area in which the animal is naturally found, the region in which it is endemic.

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

polygynandrous

the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.

riparian

Referring to something living or located adjacent to a waterbody (usually, but not always, a river or stream).

seasonal breeding

breeding is confined to a particular season

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

soil aeration

digs and breaks up soil so air and water can get in

solitary

lives alone

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

terrestrial

Living on the ground.

territorial

defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement

visual

uses sight to communicate

Ref­er­ences

Na­ture­Serve. 2013. "Ophio­gom­phus howei - Brom­ley, 1924" (On-line). Na­ture­Serve. Ac­cessed March 26, 2014 at http://​explorer.​natureserve.​org/​servlet/​NatureServe?​searchName=Ophiogomphus+howei+.

The Uni­ver­sity of Ari­zona. 1997. "The Uni­ver­sity of Ari­zona Cen­ter for In­sect Sci­ence Ed­u­ca­tion Out­reach" (On-line). In­sect In­for­ma­tion: Life Cy­cles. Ac­cessed April 28, 2014 at http://​insected.​arizona.​edu/​insectinfo.​htm.

Ab­bott, J., N. Don­nelly. 2013. "Ophio­gom­phus howei" (On-line). IUCN Red List of Threat­ened Species. Ac­cessed March 26, 2014 at http://​www.​iucnredlist.​org/​details/​summary/​15366/​0.

Bradeen, B., D. Boland. 2004. Spa­tial and Tem­po­ral Seg­re­ga­tion Among Six Species of Co­ex­ist­ing Ophio­gom­phus (Odonata: Gom­phi­dae) in the Aroos­t­ook River, Maine. North­east­ern Nat­u­ral­ist, 11: 295-312.

Brunelle, P. 2008. "COSEWIC As­sess­ment and Sta­tus Re­port on the Pygmy Snake­tail Ophio­gom­phus howei in Canada" (On-line). Ac­cessed March 26, 2014 at http://​www.​queticofoundation.​org/​pdf/​namakan_​pygmy_​snaketail.​pdf.

Hamill, S. 2013. "Re­cov­ery Strat­egy for the Pygmy Snake­tail (Ophio­gom­phus howei) in On­tario" (On-line). On­tario Re­cov­ery Strat­egy Se­ries. Ac­cessed March 26, 2014 at http://​www.​mnr.​gov.​on.​ca/​stdprodconsume/​groups/​lr/@​mnr/@​species/​documents/​document/​stdprod_​099158.​pdf.

Ham­mond, G. 2014. "BioKIDS" (On-line). Anisoptera. Ac­cessed April 23, 2014 at http://​www.​biokids.​umich.​edu/​critters/​Anisoptera/​.

Har­ris, W., D. For­man, R. Bat­tell, M. Bat­tell, A. Nel­son, P. Brain. 2011. Odonata colour: more than meets the eye?. In­ter­na­tional Jour­nal of Odona­tol­ogy, 14: 281-289. Ac­cessed April 23, 2014 at http://​dx.​doi.​org/​10.​1080/​13887890.​2011.​623981.

Kennedy, J., H. White III. 1979. De­scrip­tion of the Nymph of Ophio­gom­phus howei (Odonata: Gom­phi­dae). Proc. En­to­mol. Soc. Wash., 81: 64-69.

Lee, Y. 2009. "Spe­cial an­i­mal ab­stract for Ophio­gom­phus howei (pygmy snake­tail)" (On-line). Ac­cessed March 26, 2014 at http://​mnfi.​anr.​msu.​edu/​abstracts/​zoology/​Ophiogomphus_​howei.​pdf.

Ten­nessen, K. 1993. New Dis­tri­b­u­tion Records for Ophio­gom­phus howei (Odonata: Gom­phi­dae). Great Lakes En­to­mol­o­gist, 26: 245.