Somatochlora hineana

Williamson, 1931

Hine's Emerald

G2Imperiled (G2G3) Found in 3 roadless areas NatureServe Explorer →
G2ImperiledGlobal Rank
Least concernIUCN
Very high - highThreat Impact
Hine's emerald dragonfly (Somatochlora hineana). Photo by U.S. Fish & Wildlife Service, Public Domain (U.S. Government Work), via ECOS.
U.S. Fish & Wildlife Service, https://www.usa.gov/government-works
Identity
Unique IDELEMENT_GLOBAL.2.115545
Element CodeIIODO32110
Record TypeSPECIES
ClassificationSpecies
Classification StatusStandard
Name CategoryInvertebrate Animal
IUCNLeast concern
Endemicoccurs (regularly, as a native taxon) in multiple nations
KingdomAnimalia
PhylumArthropoda
ClassInsecta
OrderOdonata
FamilyCorduliidae
GenusSomatochlora
Other Common Names
Cordulie de Hine (FR) Hine's emerald (EN) Hine's Emerald Dragonfly (EN)
Concept Reference
Paulson, D.R. and S.W. Dunkle. 1999. A checklist of North American Odonata. Slater Museum of Natural History, University of Puget Sound Occasional Paper, 56: 86 pp. Available: http://www.ups.edu/x7015.xml.
Taxonomic Comments
Note similarities in appearance and shared habitat with Somatochlora tenebrosa (Walker and Smentowsky, 2003). Genetic analysis of haplotype distribution in related Somatochlora species (Somatochlora tenebrosa, Somatochlora linearis, Somatochlora ensignera, Somatochlora hineana) revealed greater genetic diversity in the unglaciated portion of the species' range, and lower diversity in the northern glaciated portion (Purdue et al., 1999). Genetic analysis of varying populations is underway via non-lethal tissue sampling (Monroe et al., 2010).
Conservation Status
Rank MethodExpertise without calculation
Review Date2016-08-02
Change Date1998-02-19
Edition Date2011-09-01
Edition AuthorsCordeiro, J. (2011), Schweitzer, D.F.
Threat ImpactVery high - high
Range Extent1000-20,000 square km (about 400-8000 square miles)
Number of Occurrences21 - 80
Rank Reasons
Less than 50 estimated occurrences are known (some are not viable and several can be lumped into metapopulations); most of which are small and disjunct. The species is extirpated in Ohio, Alabama, and Indiana; some other extant occurrences are threatened with habitat destruction or degradation. Potential viability is poor or unclear for a substantial number of occurrences although populations are somewhat stable following federal listing and designation of critical habitat.
Range Extent Comments
This is primarily a species of the Great Lakes region that was originally only known from Ohio and Indiana (Bick, 1983), but additional investigations also found locations in Illinois, Wisconsin (Vogt and Cashatt, 1990; 1991; 1994), Michigan and Missouri (USFWS, 2001). In the summer of 1997 it was found on the Upper Peninsula of Michigan in Mackinac County and in 2007 it was found at a wetland complex in southern Ontario (Ontario CDC has details). A single adult male has been reliably reported from Alabama. Also, recently recorded from Missouri (Walker and Smentowsky, 2003) which suggests there may be more populations in the southern part of potential range. It is apparently extirpated from Indiana and Ohio (USFWS, 1995; 2001).
Occurrences Comments
Probably > 50 occurrences globally (Vogt, pers. comm. 1998). Currently known from 42 locations (not all viable): 9 in Illinois (Will, Cook, DuPage Cos.; most not viable), 20 in Wisconsin (Door, Kewaunee, Ozaukee Cos.), 10 in Michigan (Mackinac, Presque Isle, Alpena Cos.), and at least 3 sites in Missouri (Reynolds, Iron Cos.) (USFWS, 2001). It has been searched for intensively in Illinois and Wisconsin. In addition, there are four historic occurrences in Ohio, one in Indiana, and one in Alabama (USFWS, 2001). The first Canadian occurrence was documented in 2007 in Simcoe County, Ontario (Colin Jones, ON CDC, pers. comm., July 2007).
Threat Impact Comments
Extant occurrences are threatened by the following activities: petroleum refineries and other heavy industry, a proposed highway project, quarrying, urban non-point water pollution, and ATV use in Illinois; agricultural non-point water pollution (surface and groundwater) and recreational development in Wisconsin. Most significant threats are habitat/alteration/destruction plus fragmentation from development of commercial and residential areas, quarrying, creating landfills, constructing pipelines, and filling of wetlands. Habitats are often closely associated with surface dolomite deposits which are often quarried. Changes in surface or subsurface hydrology has the potential to reduce suitable breeding habitat. Contamination from landfills (including leaching) and chemical fertilizer and pesticide application is a past and potential future threat. Secondary threats include off-road and highway vehicle mortality and associated mortality from roadway development as well as predation (probably minimal) (USFWS, 2001). The known breeding sites in Illinois occur along the Des Plaines River floodplain, which has been fragmented by industrial and urban development (Cashatt, 1991). In Wisconsin, land development for agriculture, light industry, and tourism are principal threats (Vogt and Cashatt, 1990). Off-road vehicle use and possible logging, creation of water impoundments, real estate development, road development and maintenance, pipeline construction, and changes in hydrology are potential threats in Michigan (Steffens, 1997).
Ecology & Habitat

Description

It is a fairly large metallic brown dragonfly with 2 yellow stripes on each side of the thorax, and in life, bright green eyes. (Needham and Westfall, 1955; Williamson, 1931). Adults have wings that are clear and may have an amber hue towards the base of the hind wings. After emerging as an adult, the eyes are initially brown and turn emerald green within 1 to 3 days. Toward the end of the adult life span, the wings may turn from clear to a slightly opaque, smoky color (USFWS, 2001).

Diagnostic Characteristics

Distinctive shapes of terminal appendages and ovipositors separate adults from other species. The species is distinguished from all other Somatochlora by its dark metallic green thorax with two distinct, creamy-yellow lateral lines, and distinctly shaped male terminal appendage. The wings are clear and may have an amber hue towards the base of the hind wings. Other species of Somatochlora that occur in the same range that may be confused include Somatochlora linearis, Somatochora tenebrosa, Somatochlora ensigera, Somatochlora elongata, and Somatochlora williamsoni; but they are all distinguished by the shape of terminal appendages and ovipositors (USFWS, 2001). Male cerci unique, bent downward at a right angle near the tip, the female ovipositor is a pointed trough extending at a 45 degree angle from the abdomen, and the female cerci are longer than abdominal segments 9+10. Note similarities in appearance and shared habitat with Somatochlora tenebrosa (Walker and Smentowsky, 2003).


No one larval character has been found to easily and reliably differentiate larvae from Somatochlora linearis, Somatochlora tenebrosa, Somatochlora ensigera, Somatochlora elongata, and Somatochlora williamsoni. Most Somatochlora hineana larvae have a small middorsal hook on segment three, but Somatochlora minor does as well. The earliest instars of S. hineana larvae have fewer dorsal hooks than later instars (Zercher, 2001). Other characters include head width, metatibial length, palpal crenulation setae, and total length; and are discussed in detail in Crashatt and Vogt (2001).

Habitat

In Illinois and Wisconsin, adults of this species occurs in shallow, calcareous seepage marshes; or marshy margins of small, sluggish, calcareous streams overlaying dolomite bedrock (Vogt and Cashatt, 1994). The seepage marshes are often dominated by Typha spp. and can be broadly defined as fen or fen-like communities. Larval microhabitat in Wisconsin is in shallow seepage along the edges of sluggish streamlets that meander through dense cattail seepage marsh (exuviae usually attached to Typha angustifolia) (Vogt and Cashatt, 1994). The larvae also are able to use the wet burrows of the crayfish Cambarus diogenes during dry periods. The species lives in wetlands dominated by grass or grass-like plants that are groundwater fed and shallow. Soil types range from organic muck to mineral soils like marl. A nearby forest edge is also important (USFWS, 2001). Larval habitat may be important in determining distribution.

Ecology

Larval individuals can occur in small clusters within their habitat and remain independent. Larval individuals may overwinter in crayfish burrows. Individuals are well adapted to survive drought conditions (USFWS, 2001).

Reproduction

Females most likely lay more than 500 eggs during their lives. After an egg is hatched, larvae spend 2 to 4 years in small streamlets, foraging and molting as they grow. Larvae begin to emerge as adults possibly as early as late May in Illinois and late June in Wisconsin and continue to emerge throughout the summer. Known flight season lasts up to early October in Illinois and to late August in Wisconsin. Fully adult dragonflies can live at least 14 days and may live 4 to 6 weeks (Soluk et al., 1996: Mierzwa et al., 1995). Copulating pairs have been observed from early June to late August in Illinois and from late July in Wisconsin. Females oviposit by repeatedly dipping their abdomens up to 200 times in shallow water from June to late August in Illinois and early to late July in Wisconsin; usually in seepage marshes, seepage sedge meadows, sedge hummocks, muck along sluggish water, and in small muck-bottomed pools (see Vogt and Cashatt, 1994; Soluk et al., 1996; USFWS, 2001).
Palustrine Habitats
HERBACEOUS WETLANDBog/fen
Other Nations (2)
CanadaN1
ProvinceRankNative
OntarioS1Yes
United StatesN2
ProvinceRankNative
WisconsinS1Yes
OhioSXYes
IndianaSXYes
IllinoisS1Yes
MichiganS1Yes
AlabamaSHYes
MissouriS2Yes
Threat Assessments
ThreatScopeSeverityTiming
1 - Residential & commercial developmentLarge - restrictedSerious - moderateHigh (continuing)
1.1 - Housing & urban areasLarge - restrictedSerious - moderateHigh (continuing)
1.2 - Commercial & industrial areasLarge - restrictedSerious - moderateHigh (continuing)
3 - Energy production & miningRestricted (11-30%)Extreme - moderateHigh (continuing)
3.2 - Mining & quarryingRestricted (11-30%)Extreme - moderateHigh (continuing)
4 - Transportation & service corridorsRestricted (11-30%)Serious - slightHigh - moderate
4.1 - Roads & railroadsRestricted (11-30%)Serious - slightHigh - moderate
4.2 - Utility & service linesRestricted (11-30%)Serious - slightHigh - moderate
6 - Human intrusions & disturbanceSmall (1-10%)Slight or 1-10% pop. declineHigh - moderate
6.1 - Recreational activitiesSmall (1-10%)Slight or 1-10% pop. declineHigh - moderate
7 - Natural system modificationsLarge - restrictedSerious or 31-70% pop. declineHigh (continuing)
7.2 - Dams & water management/useLarge - restrictedSerious or 31-70% pop. declineHigh (continuing)
9 - PollutionLarge - restrictedSerious - moderateHigh (continuing)
9.1 - Domestic & urban waste waterLarge - restrictedSerious - moderateHigh (continuing)
9.2 - Industrial & military effluentsLarge - restrictedSerious - moderateHigh (continuing)
9.3 - Agricultural & forestry effluentsLarge - restrictedSerious - moderateHigh (continuing)

Roadless Areas (3)
Michigan (2)
AreaForestAcres
Government IslandHiawatha National Forest225
Round IslandHiawatha National Forest2
Missouri (1)
AreaForestAcres
Anderson Mountain Rare II Study AreaMark Twain National Forest2,741
References (36)
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  4. Cashatt, E.D. and T.E. Vogt. 2001. Description of the larva of <i>Somatochlora hineana</i> with a key to the larvae of the North American species of <i>Somatochlora </i>(Odonata: Corduliidae). International Journal of Odonatology 4(2):93-105.
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