Etheostoma spilotum

Gilbert, 1887

Kentucky Arrow Darter

G2Imperiled Found in 3 roadless areas NatureServe Explorer →
G2ImperiledGlobal Rank
Near threatenedIUCN
HighThreat Impact
Identity
Unique IDELEMENT_GLOBAL.2.105403
Element CodeAFCQC02661
Record TypeSPECIES
ClassificationSpecies
Classification StatusStandard
Name CategoryVertebrate Animal
IUCNNear threatened
Endemicendemic to a single state or province
KingdomAnimalia
PhylumCraniata
ClassActinopterygii
OrderPerciformes
FamilyPercidae
GenusEtheostoma
Synonyms
Etheostoma sagitta spilotumGilbert, 1887
Other Common Names
Cumberland Plateau Darter (EN)
Concept Reference
Lee, D. S., C. R. Gilbert, C. H. Hocutt, R. E. Jenkins, D. E. McAllister, and J. R. Stauffer, Jr. 1980. Atlas of North American freshwater fishes. North Carolina State Museum of Natural History, Raleigh, North Carolina. i-x + 854 pp.
Taxonomic Comments
Thomas et al. (2023) present multiple lines of evidence supporting the recognition of Etheostoma spilotum and E. sagitta as distinct species, with a revised diagnosis and redescription of E. spilotum. Previously, Page and Burr (2011) and Catalog of Fishes (as of early 2012) recognized E. spilotum as a distinct species, however, Page et al. (2013) did not accept this change.
Conservation Status
Rank Method Rank calculation - Biotics v2
Review Date2026-02-01
Change Date2026-02-01
Edition Date2026-02-01
Edition AuthorsHammerson, G. (2012); rev. R. L. Gundy (2026)
Threat ImpactHigh
Range Extent1000-20,000 square km (about 400-8000 square miles)
Number of Occurrences21 - 80
Rank Reasons
This species has undergone a substantial long-term decline and is extirpated from approximately 50% of the historically occupied streams. Its habitat in many areas has been severely degraded as a result of coal mining, oil and gas exploration, and logging. It now occurs in 52 streams in the upper Kentucky River drainage in Kentucky and is moderately common in some areas.
Range Extent Comments
This species is restricted to the upper Kentucky River basin in eastern Kentucky, USA, where it occupies upland streams on the Cumberland Plateau. The distribution extends from the Red River upstream including Sturgeon Creek and the North, Middle, and South forks of the Kentucky River (Thomas et al. 2023). Approximately 90% of the species’ range lies within the Central Appalachian ecoregion, and a smaller portion of populations along the northern and western edge of the range lies within the Western Allegheny Plateau ecoregion (Thomas et al. 2023). Using extant NatureServe (2026) occurrence records, range extent is estimated to be 5,140 km² (RARECAT 2025).
Occurrences Comments
This species is represented by a fairly large number of occurrences (subpopulations) and locations. It is reported to be extant in 52 streams in the following Kentucky River tributaries (and smaller tributary watersheds): (1) Red River (Rock Bridge Fork of Swift Camp Creek); (2) Sturgeon Creek (Travis, Wild Dog, and Granny Dismal creeks); (3) Silver Creek; (4) North Fork Kentucky River (Troublesome, Quicksand, Frozen, Holly, Lower Devil, Walker, and Hell creeks); (5) Middle Fork Kentucky River (Big Laurel, Rockhouse, Hell for Certain, and Squabble creeks); and (6) South Fork Kentucky River (Red Bird River, Hector Branch, and Goose, Bullskin, Buffalo, and Lower Buffalo creeks) (USFWS 2022, Thomas et al. 2023). The largest cluster of occurrences is within the Red Bird River watershed (South Fork Kentucky River drainage) (Thomas et al. 2023). Blanton et al. (2019) found the species to consist of 9 genetically distinct populations.
Threat Impact Comments
This darter can tolerate moderate siltation, but heavy siltation and acid runoff from regional surface mining for coal has eliminated many populations (Page and Burr 1991, Etnier and Starnes 1993, Hitt et al. 2016). All of the range is in coal-producing areas (Etnier and Starnes 1993). USFWS (2022) noted there are 97 active surface mining permits in this species' range. High conductivity, which negatively impacts intercellular ion-transport mechanisms regulating osmoregulation and acid/base balance, caused by sulfate pollution from coal mining has been shown to decrease abundance of this species (Hitt et al. 2016, Blanton et al. 2019). High conductivity can even make affected stream segments unsuitable for this species and effectively creates habitat fragmentation within a single stream (Blanton et al. 2019, Watson et al. 2024). Loss of only 10% forest cover can cause declines in abundance and even fragment habitat in streams (Culley et al. 2025). Runoff pollution, stream channelization, and any number of causes of sedimentation also reduce abundance of this species (USFWS 2010, Hitt et al. 2016, USFWS 2022, Watson et al. 2024). Severe flooding from increasingly severe thunderstorms is suspected of negatively impacting local populations (USFWS 2022).

USFWS (2010) summarized threats as follows: Habitat has been severely degraded and limited by water pollution from surface coal mining and gas exploration activities; removal of riparian vegetation; stream channelization; increased siltation associated with poor mining, logging, and agricultural practices; and deforestation of watersheds. These threats are (1) widespread across the range; (2) imminent (the effects are manifested immediately and will continue); and (3) severe (stressors are of high intensity or high strength and can lead to mortality). The severity (or intensity) of these threats, especially impacts from mining and gas exploration activities, is high - these activities can permanently alter stream water quality (e.g., elevated conductivity) by contributing sediment, dissolved metals, and other solids to streams supporting populations. These water quality changes can be permanent and render these habitats unsuitable for the darter. Recent and past research has demonstrated that this darter is intolerant of these conditions, and it has been eliminated from a number of streams across its range. Current regulatory mechanisms have been inadequate to prevent these impacts. The small, remnant nature of many populations may prohibit the natural interchange of genetic material between these populations, and the small population size may reduce the reservoir of genetic diversity within populations. This can lead to inbreeding depression and reduced fitness of individuals. It is possible that some populations are below the effective population size required to maintain long-term genetic and population viability. No available information indicates that the magnitude or imminence of these threats is likely to be appreciably reduced in the foreseeable future.
Ecology & Habitat

Habitat

Habitat includes upland creeks and streams, generally in headwaters, but juveniles and sometimes adults also sometimes are found in larger streams; generally this darter occurs in slow to moderate current in cool, sluggish pools or areas above and below riffles (avoids swift currents) over bedrock, rubble, cobble, and pebble, often interspersed with sandy areas (Burr and Warren 1986, Etnier and Starnes 1993). This darter is common only in intermittently flowing first- or second-order creeks, preferring protective stones near the bank, or ledges and recesses at stream margins (Kuehne and Barbour 1983, Etnier and Starnes 1993). Spawning occurs apparently in riffles in water about 5-15 centimeters deep (Kuehne and Barbour 1983) or under or near rocks in raceways (Etnier and Starnes 1993).

Reproduction

Spawning probably peaks in early spring.
Other Nations (1)
United StatesN2
ProvinceRankNative
KentuckyS2Yes
Threat Assessments
ThreatScopeSeverityTiming
3 - Energy production & miningLarge (31-70%)Moderate - slightHigh (continuing)
3.2 - Mining & quarryingLarge (31-70%)Moderate - slightHigh (continuing)
7 - Natural system modificationsSmall (1-10%)Moderate - slightHigh (continuing)
7.2 - Dams & water management/useSmall (1-10%)Moderate - slightHigh (continuing)
9 - PollutionLarge (31-70%)Extreme - seriousHigh (continuing)
9.1 - Domestic & urban waste waterSmall (1-10%)Moderate - slightHigh (continuing)
9.1.2 - Run-offSmall (1-10%)Moderate - slightHigh (continuing)
9.2 - Industrial & military effluentsLarge (31-70%)Extreme - seriousHigh (continuing)
9.3 - Agricultural & forestry effluentsRestricted (11-30%)Moderate or 11-30% pop. declineHigh (continuing)
11 - Climate change & severe weatherPervasive (71-100%)UnknownHigh (continuing)
11.4 - Storms & floodingPervasive (71-100%)UnknownHigh (continuing)

Roadless Areas (3)
Idaho (1)
AreaForestAcres
Bear CreekCaribou-Targhee National Forest118,582
Kentucky (1)
AreaForestAcres
WolfpenDaniel Boone National Forest2,835
Virginia (1)
AreaForestAcres
North Fork PoundJefferson National Forest4,757
References (22)
  1. Arnold, C. 2016. Movement patterns of the Kentucky arrow darter (<i>Etheostoma spilotum</i>), frecklebelly darter (<i>Percina </i><i>stictogaste</i>r), and southern redbelly dace (<i>Chrosomus erythrogaster</i>) in Elisha Creek and Gilbert's Big Creek, Red Bird River, Kentucky. M. S. thesis. Eastern Kentucky University Richmond, KY. 34 pp.
  2. Baxter, J. 2015. Distribution, movement, and ecology of <i>Etheostoma spilotum</i> (Gilbert), the Kentucky arrow darter, in Gilberts Big Creek and Elisha Creek, Red Bird River Basin, Clay and Leslie counties, Kentucky. M.S. thesis. Eastern Kentucky University, Richmond, KY. 51 pp.
  3. Blanton, R. E., M. F. Cashner, M. R. Thomas, S. L. Brandt, and M. A. Floyd. 2019. Increased habitat fragmentation leads to isolation among and low genetic diversity within populations of the imperiled Kentucky Arrow Darter (<i>Etheostoma sagitta spilotum</i>). Conservation Genetics 20: 1009-1022. doi: doi: 10.1007/s10592-019-01188-y
  4. Burr, B. M., and M. L. Warren, Jr. 1986a. Distributional atlas of Kentucky fishes. Kentucky Nature Preserves Commission, Scientific and Technical Series No. 4, Frankfort, Kentucky. 398 pp.
  5. Culley, A. V., R. A. Watson, C. G. Haase, M. R. Thomas, S. L. Brandt, M. A. Floyd, and R. E. Blanton. 2025. Loss of forest cover leads to population isolation in an imperiled, headwater-specialist fish. Landscape Ecology 40: 147. doi: doi: 10.1007/s10980-025-02163-4
  6. Etnier, D. A., and W. C. Starnes. 1993. The fishes of Tennessee. University of Tennessee Press, Knoxville, Tennessee. xiv + 681 pp.
  7. Fricke, R., Eschmeyer, W. N. &amp; R. van der Laan (eds). 2022. Eschmeyer's Catalog of Fishes: genera, species, references.(http://researcharchive.calacademy.org/research/ichthyology/catalog/fishcatmain.asp). Electronic version 2022.
  8. Hitt, N. P. M. Floyd, M. Compton, and K. McDonald. 2016. Threshold responses of blackside dace (<i>Chrosomus cumberlandensis</i>) and Kentucky arrow darter (<i>Etheostoma spilotum</i>) to stream conductivity. Southeastern Naturalist 15(1):41-60. https://doi.org/10.1656/058.015.0104
  9. Jelks, H. L., S. J. Walsh, N. M. Burkhead, S. Contreras-Balderas, E. Díaz-Pardo, D. A. Hendrickson, J. Lyons, N. E. Mandrak, F. McCormick, J. S. Nelson, S. P. Platania, B. A. Porter, C. B. Renaud, J. Jacobo Schmitter-Soto, E. B. Taylor, and M.L. Warren, Jr. 2008. Conservation status of imperiled North American freshwater and diadromous fishes. Fisheries 33(8):372-407.
  10. Kuehne, R. A., and R. W. Barbour. 1983. The American Darters. University Press of Kentucky, Lexington, Kentucky. 177 pp.
  11. Lee, D. S., C. R. Gilbert, C. H. Hocutt, R. E. Jenkins, D. E. McAllister, and J. R. Stauffer, Jr. 1980. Atlas of North American freshwater fishes. North Carolina State Museum of Natural History, Raleigh, North Carolina. i-x + 854 pp.
  12. NatureServe. 2026. NatureServe Network Biodiversity Location Data. NatureServe, Arlington, Virginia.
  13. Page, L. M. 1983a. Handbook of Darters. T. F. H. Publications, Inc., Neptune City, New Jersey. 271 pp.
  14. Page, L. M., and B. M. Burr. 1991. A field guide to freshwater fishes: North America north of Mexico. Houghton Mifflin Company, Boston, Massachusetts. 432 pp.
  15. Page, L. M., and B. M. Burr. 2011. Peterson field guide to freshwater fishes of North America north of Mexico. Second edition. Houghton Mifflin Harcourt, Boston. xix + 663 pp.
  16. Page, L. M., K. E. Bemis, T. E. Dowling, H.S. Espinosa-Pérez, L.T. Findley, C. R. Gilbert, K. E. Hartel, R. N. Lea, N. E. Mandrak, M. A. Neigbors, J. J. Schmitter-Soto, and H. J. Walker, Jr. 2023. Common and scientific names of fishes from the United States, Canada, and Mexico. Eighth edition. American Fisheries Society (AFS), Special Publication 37, Bethesda, Maryland, 439 pp.
  17. <p>NatureServe's Rapid Analysis of Rarity and Endangerment Conservation Assessment Tool (RARECAT). 2025. Version: 2.1.1 (released April 04, 2025).</p>
  18. Thomas, M. R., R. E. Blanton, A. Ghezelayagh, and T. J. Near. 2023. Species-level recognition and redescription of the Kentucky Arrow Darter, <i>Etheostoma spilotum</i> Gilbert (Percidae: <i>Litocara</i>). Bulletin of the Peabody Museum of Natural History 64(1):39-80.
  19. U.S. Fish and Widlife Service (USFWS). 2010.<i> Etheostoma sagitta</i> ssp. <i>spilotum</i>. Species assessment and listing priority assignment form.
  20. U.S. Fish and Wildlife Service (USFWS). 2022. Kentucky arrow darter (<i>Etheostoma spilotum</i>) status review: summary and evaluation. Southeast Region, Kentucky Ecological Services Field Office Frankfort, Kentucky. 18 pp.
  21. Warren, M. L., Jr., B. M. Burr, S. J. Walsh, H. L. Bart, Jr., R. C. Cashner, D. A. Etnier, B. J. Freeman, B. R. Kuhajda, R. L. Mayden, H. W. Robison, S. T. Ross, and W. C. Starnes. 2000. Diversity, distribution, and conservation status of the native freshwater fishes of the southern United States. Fisheries 25(10):7-31.
  22. Watson, R. A., A. V. Culley, C. G. Haase, M. R. Thomas, S. L. Brandt, M. A. Floyd, and R. E. Blanton. 2024. Instream barriers contribute to population isolation of a small- bodied, benthic, headwater- specialist fish (Percidae). Ecology of Freshwater Fish 33: e12769. doi: 10.1111/eff.12769