Geographic Range
Chrysops excitans
is a common and widespread deer fly, occurring across Canada and Alaska, south to
California (as an isolated population) in the west and New Jersey and West Virginia
in the east.
Habitat
Chrysops excitans
larvae are aquatic and are found close to shore in both lentic and lotic waters,
such as lakes, ponds, swamps, marine beaches, and rivers. Adults occur in the forests,
grasslands, taiga, and mountains near the aquatic habitats from which they emerged.
- Habitat Regions
- temperate
- terrestrial
- freshwater
- Terrestrial Biomes
- taiga
- savanna or grassland
- forest
- mountains
- Aquatic Biomes
- lakes and ponds
- rivers and streams
- Other Habitat Features
- riparian
Physical Description
Chrysops excitans is a medium sized fly (9 to 12 mm) with a mostly black body. Males are holoptic (eyes touch) and females have eyes separated on the head. The clypeus is black with a yellow, pruinose stripe. The wings have a characteristic black marking mid-wing which does not reach the posterior margin and a clear wing apex. The abdomen has dorsal median triangles which are especially large on the second segment. The second and third abdominal segments are often largely yellow or orange. This species is most easily confused with Chrysops dawsoni , from which it can be distinguished by the yellow triangle on the second abdominal segment. The female's mouthparts are specialized for biting and consist of a labium, a pair each of sharp, knife-like maxillae and mandibles, a hypopharynx and a labrum.
The eggs are fusiform and approximately 2 mm long. Larvae are tapered at both ends
and have 11 segments. The first seven abdominal segments have a pair of dorsal, lateral
and ventral prolegs. The pupae are obtect with the head, thorax, abdomen and appendage
sheaths distinct.
- Other Physical Features
- ectothermic
- heterothermic
- bilateral symmetry
- Sexual Dimorphism
- sexes shaped differently
Development
Deer flies are holometabolous and progress through egg, larval, pupal and adult stages.
A blood meal is necessary for egg production. Lake & Burger (1980) found that some
species, including
C. excitans
seem to be anautagenous, and probably need a blood meal even to mature the first
batch of eggs. Other species, including
C. ater
are autogenous, and can lay one batch of eggs without a blood meal. Results from
Magnarelli (1976) differed for
C. ater
, indicating that there may be some population variation in this characteristic. Magnarelli
& Anderson (1977, 1981) also found that nectar feeding by females of some species
may be a significant factor affecting the yolking of eggs and female success. Eggs
are laid attached to each other and to a substrate (over or near water) in masses
of less than 100 eggs. Embyronic development is usually complete in about 5 days.
Almost all eggs hatch simultaneously after some warming by the sun. Larvae inhabit
the water below and pass through approximately 6 instars. Larval development is about
9 to 10 months. The larvae then migrate to a position where they will not be submerged
for extended periods and pupate. The pupal period lasts about 2 weeks. Adults normally
emerge form pupal cases in the morning and their wings soon expand and harden, making
flight possible.
- Development - Life Cycle
- metamorphosis
- diapause
Reproduction
There is no available information on this species, but in other
Chrysops
species, males use either a hovering or non-hovering flight behavior as they seek
mates. This has been most extensively studied in the salt marsh species
C. atlanticus
and
C. fuliginosus
. Leprince, Lewis & Parent (1983) studied male behavior in a variety of
Chrysops
species (not including
C. excitans
) in Quebec and found that all species used a strategy of waiting on nearby vegetation
and then flying out after any passing flies, including potential female mates. In
the salt marsh species, mating occurred mainly in the morning at cooler temperatures,
before oviposition and feeding later in the day, at higher temperatures. Some work
suggests that females may mate at least two times during their adult lifespan.
- Mating System
- polygynandrous (promiscuous)
Females generally take about 4 to 8 days after a blood meal to mature a batch of eggs.
These are laid as a group, usually on the stems or underside of leaves above or near
water. They are usually laid on warm, sunny days in the morning. Both males and females
are known to take nectar meals for an energy source, and this seems to be an important
source of nutrition.
- Key Reproductive Features
- iteroparous
- seasonal breeding
- gonochoric/gonochoristic/dioecious (sexes separate)
- sexual
- fertilization
- oviparous
Females of
Chrysops excitans
take blood meals to provide yolk and provisioning in the eggs. They also lay the
eggs in a spot over suitable habitats for the larvae to drop into. Otherwise, they
do not provide any other parental care.
- Parental Investment
-
pre-hatching/birth
-
provisioning
- female
-
provisioning
Lifespan/Longevity
Chrysops excitans
will hatch from eggs in summer, overwinter as larvae, emerge from pupae in early
summer and die late summer. Lifespan is a little over a year, at most. Little is know
about the longevity of individuals as adults, but they are known to live for a number
of weeks.
Behavior
The seasonal activity of adult deer flies normally extends from late May to mid-September. Activity is the greatest on sunny days with little or no wind. Several variables are known to affect activity including barometric pressure, temperature, cloud cover, and relative humidity.
The major activity of interest in this species is biting by females for blood meals.
Because a bite is painful, blood meals are often interrupted by avoidance behaviors
of hosts. To complete a meal, females must feed on multiple host individuals, promoting
the spread of disease among the host species.
- Key Behaviors
- flies
- diurnal
- parasite
- motile
- hibernation
- daily torpor
- solitary
Home Range
Tabanid flies will disperse 1 to 2 km from their breeding sites.
Communication and Perception
Although Chrysops excitans has not been studied, tabanids in general use both visual and chemical cues to perceive their environment and communicate with other individuals. Males use vision to help locate mates, and females use vision during their search for hosts and oviposition locations.
Chemicals are obviously part of the attraction that females have to hosts, because
traps baited with CO2 or octenol are known to attract feeding females. Females also
see attracted thermally to potential hosts. They are especially attracted to dark
surfaces, and black ball traps are regularly used to collect individuals.
- Perception Channels
- visual
- infrared/heat
- ultraviolet
- tactile
- chemical
Food Habits
The larvae apparently feed on organic matter in moist soil but their specific feeding
habits are unknown. Adult males feed on nectar (which is their primary energy source)
and pollen. Females feed on nectar as a major energy source, but also use honeydew
secreted by
Hemiptera
and rotting fruit. Adult females feed on blood to yolk eggs, using a variety of vertebrates.
Deer and humans are frequently targeted, but cattle, sheep, hogs, horses and other
domestic animals are also frequent targets.
- Primary Diet
- carnivore
- herbivore
- detritivore
- Animal Foods
- blood
- Plant Foods
- fruit
- nectar
- pollen
- Other Foods
- detritus
Predation
Chrysops
have been recorded as prey for birds, amphibians, dragonflies,
robber flies
, and wasps (including
Vespula
,
Crabro
, and
Bembix
).
Ecosystem Roles
Chrysops excitans
males may pollinate the flowers on which they feed. They are also food for other
animals. Females are ectoparasites and require blood meals from a variety of vertebrates
to mature their eggs. They feed on deer, humans, cattle, sheep, hogs, horses and other
domestic animals. As blood feeders, they can also transmit disease to their hosts.
Chrysops excitans
is also used as a host to a variety of parasites.
- Ecosystem Impact
- pollinates
- parasite
- deer, Cervidae
- humans, Homo sapiens
- cattle, Bos
- sheep, Ovis aries
- pigs, Sus
- horses, Equus ferus caballus
- wasps, Telenomus spp.
- wasps, Pteromalidae
- flies, Tachinidae
- bee flies, Bombyliidae
- wasps, Trichogramma spp.
- nematodes, Nematoda
- Trypanosoma
- Spiroplasma spp.
Economic Importance for Humans: Positive
Plant pollination may occur as a result of the feeding habits (pollenophagy) of adult flies, but this is certainly minimal.
Economic Importance for Humans: Negative
Deer flies are known as pests because the female will feed on the blood of certain
mammals, especially humans.
Chrysops
is known to be potential vectors for anthrax, tularemia, anaplasmosis, hog cholera,
equine infectious anemia and filariasis (Lyon 2013). Tabanid flies may also be an
occasional vector of Lyme Disease. The direct impact on humans in North America is
mainly as an annoyance, but serious damage can result in domestic animals, due to
biting and disease transmission.
- Negative Impacts
-
injures humans
- bites or stings
- carries human disease
- causes or carries domestic animal disease
Conservation Status
This species is abundant and requires no special status.
Additional Links
Contributors
Brian Steel (author), University of Michigan Biological Station, Brian Scholtens (editor), University of Michigan Biological Station, Angela Miner (editor), Animal Diversity Web Staff.
- 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.
- native range
-
the area in which the animal is naturally found, the region in which it is endemic.
- 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.
- freshwater
-
mainly lives in water that is not salty.
- taiga
-
Coniferous or boreal forest, located in a band across northern North America, Europe, and Asia. This terrestrial biome also occurs at high elevations. Long, cold winters and short, wet summers. Few species of trees are present; these are primarily conifers that grow in dense stands with little undergrowth. Some deciduous trees also may be present.
- tropical savanna and grassland
-
A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.
- savanna
-
A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.
- temperate grassland
-
A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.
- forest
-
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
- mountains
-
This terrestrial biome includes summits of high mountains, either without vegetation or covered by low, tundra-like vegetation.
- marsh
-
marshes are wetland areas often dominated by grasses and reeds.
- swamp
-
a wetland area that may be permanently or intermittently covered in water, often dominated by woody vegetation.
- bog
-
a wetland area rich in accumulated plant material and with acidic soils surrounding a body of open water. Bogs have a flora dominated by sedges, heaths, and sphagnum.
- riparian
-
Referring to something living or located adjacent to a waterbody (usually, but not always, a river or stream).
- ectothermic
-
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
- 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.
- 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.
- 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.
- diapause
-
a period of time when growth or development is suspended in insects and other invertebrates, it can usually only be ended the appropriate environmental stimulus.
- polygynandrous
-
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
- 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).
- 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
- fertilization
-
union of egg and spermatozoan
- internal fertilization
-
fertilization takes place within the female's body
- oviparous
-
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
- diurnal
-
- active during the day, 2. lasting for one day.
- parasite
-
an organism that obtains nutrients from other organisms in a harmful way that doesn't cause immediate death
- motile
-
having the capacity to move from one place to another.
- hibernation
-
the state that some animals enter during winter in which normal physiological processes are significantly reduced, thus lowering the animal's energy requirements. The act or condition of passing winter in a torpid or resting state, typically involving the abandonment of homoiothermy in mammals.
- solitary
-
lives alone
- visual
-
uses sight to communicate
- tactile
-
uses touch to communicate
- chemical
-
uses smells or other chemicals to communicate
- visual
-
uses sight to communicate
- infrared/heat
-
(as keyword in perception channel section) This animal has a special ability to detect heat from other organisms in its environment.
- tactile
-
uses touch to communicate
- chemical
-
uses smells or other chemicals to communicate
- detritus
-
particles of organic material from dead and decomposing organisms. Detritus is the result of the activity of decomposers (organisms that decompose organic material).
- parasite
-
an organism that obtains nutrients from other organisms in a harmful way that doesn't cause immediate death
- causes or carries domestic animal disease
-
either directly causes, or indirectly transmits, a disease to a domestic animal
- carnivore
-
an animal that mainly eats meat
- sanguivore
-
an animal that mainly eats blood
- herbivore
-
An animal that eats mainly plants or parts of plants.
- nectarivore
-
an animal that mainly eats nectar from flowers
- detritivore
-
an animal that mainly eats decomposed plants and/or animals
References
Anderson, J. 1971. Autogeny and mating and their relationship to biting in the saltmarsh deer fly, Chrysops atlanticus ( Diptera : Tabanidae ). Ann. Entomol. Soc. Amer. , 64/6: 1421-1424.
Arnett, R. 1993. American Insects: A Handbook of the Insects of America North of Mexico . Gainesville, Florida: Crane Press, Inc..
Bland, R., H. Jacques. 1978. How to Know the Insects . Dubuque, Iowa: William C. Brown Company.
Burnett, A., K. Hays. 1974. Some influence of meteorological factors on flight activity of female horse flies ( Diptera : Tabanidae ). Environ. Entomol. , 3: 515-521.
Catts, E., W. Olkowski. 1972. Biology of Tabanidae ( Diptera ): mating and feeding behavior of Chrysops fulliginosus . Environ. Entomol. , 1/4: 448-453.
Cilek, J. 2000. Evaluation of "Tred-Not Deerfly Patches" against host-seeking deer flies ( Diptera : Tabanidae ) in north Florida. Florida Entomologist , 83/4: 476-480.
Easton, E. 1983. The horse flies and deer flies of South Dakota. New state records and an annotate checklist ( Diptera : Tabanidae ). Entomol. News , 94/5: 196-200.
Golini, V., R. Wright. 1978. Relative abundance and seasonal distribution of Tabanidae ( Diptera ) near Guelph, Ontario. Canadian Entomologist , 110: 385-398.
Hays, K. 1956. A synopsis of the Tabanidae ( Diptera ) of Michigan. Misc. Publ. Museum Zoology, Univ. Michigan , 98: 1-79.
Hine, J. 1903. Tabanidae of Ohio . Columbus, OH: The Ohio State University.
Iranpour, M., T. Galloway. 2004. Three new Nearctic species of Telenomus ( Hymenoptera : Scelionidae ) attacking Tabanidae eggs. Canadian Entomologist , 136: 43-60.
Iranpour, M., A. Schurko, G. Klassen, T. Galloway. 2004. DNA fingerprinting of tabanids ( Diptera : Tabanidae ) and their respective egg masses using PCR - restriction fragment profiling. Canadian Entomologist , 136: 605-619.
Janzen, T., F. Hunter. 1998. Honeydew sugars in wild-caught female deer flies ( Diptera : Tabanidae ). J. Medical Entomol. , 35/5: 685-689.
Jones, C., D. Anthony. 1964. The Tabanidae ( Diptera ) of Florida. USDA Agric. Res. Serv. Tech. Bull. , 1295: 1-85.
Krinsky, W. 1976. Animal disease agents transmitted by horse-flies and deer flies ( Diptera : Tabanidae ). J. Medical Entomol. , 13: 225-275.
Lake, D., J. Burger. 1980. Ovarian development in adult Chrysops ( Diptera : Tabanidae ) in northern New England, with emphasis on Chrysops ater and C. mitis . J. Medical Entomol. , 17/6: 502-505.
Leprince, D., D. Lewis, J. Parent. 1983. Biology of male tabanids ( Diptera ) aggregated on a mountain summit in southwestern Quebec. Journal of Medical Entomology , 20: 608-613.
Lewis, D., D. Leprince. 1981. Horse flies and deer flies ( Diptera : Tabanidae ) feeding on cattle in southwestern Quebec. Canadian Entomologist , 113: 883-886.
Lewis, D., G. Bennet. 1977. Biting flies of the eastern maritime provinces of Canada. I. Tabanidae . Canadian Journal of Zoology , 55/9: 1493-1503.
Luger, S. 1990. Lyme Disease transmitted by a biting fly. New England Journal of Medicine , 322/24: 1752.
Lyon, W. 2013. "Horse and Deer Flies" (On-line). Accessed August 08, 2013 at http://ohioline.osu.edu/hyg-fact/2000/2115 .
Magnarelli, L., J. Anderson. 1980. Feeding behavior of Tabanidae ( Diptera ) on cattle and serologic analyses of partial blood meals. Environ. Entomol. , 9: 664-667.
Magnarelli, L., J. Anderson. 1977. Follicular development in salt marsh Tabanidae ( Diptera ) and incidence of nectar feeding with relation to gonotrophic activity. Ann. Entomol. Soc. Amer. , 70/4: 529-533.
Magnarelli, L., J. Anderson. 1981. Sugar feeding by female tabanids ( Diptera : Tabanidae ) and its relation to gonotrophic activity. J. Medical Entomol. , 18/5: 429-433.
Magnarelli, L. 1976. Physiological age of Tabanidae ( Diptera ) in eastern New York state, U. S. A.. J. Medical Entomol. , 12/6: 679-682.
McAlpine, J., B. Peterson, G. Slewell, H. Teskey, J. Vockeroth, D. Wood. 1981. Manual of Nearctic Diptera . Ottawa, Ontario: Biosystematics Research Institute.
Merrit, R., K. Cummins, M. Berg. 2008. An Introduction to the Aquatic Insects of North America . Atlanta, Georgia: Kendall Hunt Publishing.
Mihok, S., D. Carlson, P. Ndegwa. 2007. Tsetse and other biting fly responses to Nzi traps baited with octenol, phenols and acetone. Medical and Veterinary Entomol. , 21: 70-84.
Ossowski, A., F. Hunter. 2000. Distribution patterns, body size, and sugar-feeding habits of two species of Chrysops ( Diptera : Tabanidae ). Canadian Entomologist , 132: 213-221.
Pechuman, L., D. Webb, H. Teskey. 1983. The Diptera , or true flies, of Illinois. I. Tabanidae . Illinois Natural History Survey Bull. , 33/1: 1-121.
Roberts, R., R. Dicke. 1958. Wisconsin Tabanidae . Wisconsin Acad. Sciences, Arts, and Letters , 47: 23-42.
Roberts, R., R. Dicke. 1964. The biology and taxonomy of some immature Nearctic Tabanidae ( Diptera ). Ann. Entomol. Soc. Amer. , 57: 31-40.
Roberts, R. 1980. The effect of temperature on the duration of oogenesis and embryonic development in Tabanidae ( Diptera ). J. Medical Entomol. , 17/1: 8-14.
Smith, S., D. Davies, V. Golini. 1970. A contribution to the bionomics of the Tabanidae ( Diptera ) of Algonquin Park, Ontario: seasonal distribution, habitat preferences, and biting records. Canadian Entomologist , 102: 1461-1473.
Teskey, H. 1969. Larvae and pupae of some eastern North American Tabanidae ( Diptera ). Mem. Entomol. Soc. Canada , 101/S63: 5-147.
Teskey, H. 1990. The Horseflies and Deer flies of Canada and Alaska. Diptera : Tabanidae . Ottawa, Ontario: Biosystematics Research Center.
Thomas, A., S. Marshall. 2009. Tabanidae of Canada, east of the Rocky Mountains 1:a photographic key to the species of Chrysopinae and Pangoniinae ( Diptera : Tabanidae ). Canadian Journal of Arthropod Identification , 8/June 28: 65.
Troubridge, D., D. Davies. 1975. Seasonal changes in physiological age composition of tabanid ( Diptera ) populations in southern Ontario. J. Medical Entomol. , 12/4: 453-457.