Blackside dace (Chrosomus cumberlandensis) are found in approximately 40 tributaries of the Cumberland River in Pulaski, Laurel, McCreary, Whitley, Knox, Bell, Harlan, and Letcher counties in Kentucky, and Scott, Campbell, and Claiborne counties in Tennessee (NatureServe, 2005) and have been recently discovered in the upper Clinch River drainage in Lee County, Virginia (Pinder, M.J., personal communication). A survey of 168 upper Cumberland River streams, by Starnes and Starnes (1981) found the species to occur in 27 different drainages. A survey by O’Bara (1985) found blackside dace in 30 of 193 upper Cumberland River drainages. ("NatureServe", 2005; O'Bara, 1985; Starnes and Starnes, 1981)
Blackside dace inhabit small to medium sized streams 2.1 to 4.6 meters in width, with moderate gradient, and rarely exceeding 21 degrees Celsius (70 degrees Fahrenheit) (Biggins, 1988). According to O’Bara (1985), blackside dace occur in only moderate gradient streams that have a 60:40 riffle-pool ratio. Substrate in these streams consists of cobble-gravel in riffles and bedrock-boulder-silt in pools (O’Bara, 1985). Starnes and Starnes (1981) note that these fish are generally associated with undercut stream banks and large rocks, and they are usually found in drainages with well-vegetated watersheds and riparian zones. The riparian vegetation generally associated with blackside dace habitat includes woody species such as eastern hemlock (Tsuga canadensis), giant rhododendron (Rhododendron maximum), ironwood (Carpinus caroliniana), river birch (Betula nigra), and American sycamore (Platanus occidentalis) (O’Bara, 1985). Canopy cover at stream sections that support blackside dace is usually over 70 percent (O’Bara, 1985). (Biggins, 1988; O'Bara, 1985; Starnes and Starnes, 1981)
Blackside dace have an incomplete lateral line with 66 to 81 lateral line scales (Etnier and Starnes, 1993). Anal fin ray count is 8 to 9 and pectoral fin rays range from 14 to 16 (Etnier and Starnes, 1993). Adults range from 50 to 65 mm during the end of the second and third summers and can reach a maximum length of 76 mm (Etnier and Starnes, 1993). Adults have a single black lateral stripe or two stripes converging on the caudal peduncle, a green/gold dorsum with black speckling and a pale to brilliant scarlet belly (Biggins, 1988; Etnier and Starnes, 1993). The fins are often bright yellow with metallic silver surrounding the base of the pelvic and pectoral fins (Biggins, 1988). The yellowish fins seem to be associated with the breeding season (Etnier and Starnes, 1993). The male is more colorful and can be distuingished from the female by having a golden dorsum and well developed tubercles on the pectoral fins during the breeding season (Etnier and Starnes, 1993).
A similar species that can be found in the same watershed as blackside dace is southern redbelly dace (Chrosomus erythrogaster). Blackside dace are differentiated from southern redbelly dace by a single black lateral stripe or two stripes that converge on the caudal peduncle, where southern redbelly dace have two parallel lateral stripes (Etnier and Starnes, 1993).
Juvenile blackside dace can be confused with juvenile creek chub (Semotilus atromaculatus) and juvenile blacknose dace (Rhinichthys atratulus) (Etnier and Starnes, 1993). Creek chub are more robust and have only 51 to 54 lateral line scales, and blacknose dace are differentiated by having a frenum (Etnier and Starnes, 1993). (Biggins, 1988; Etnier and Starnes, 1993)
Little is known about the early development of blackside dace. A life span of three years is typical, with fry growing to about 30 mm by the first fall of life and reaching sexual maturity by their first spring (Etnier and Starnes 1993). During the second and third year, total lengths average 50 to 60 mm, with a maximum total length of 76 mm (Etnier and Starnes, 1993). Size ranges are broken into three age classes, which include the following: Age 0: 30 to 39 mm, Age I: 40 to 59 mm, and Age II: 60 to 79 mm (O’Bara, 1985). Biologists use the age classes to determine if blackside dace populations are reproducing and viable. (Etnier and Starnes, 1993; O'Bara, 1985)
Little is known about the mating systems of blackside dace. Spawning occurs during the spring, from April to June. Males gather in small groups during spawning and several males fertilize the eggs of each female as she deposits them (USFWS, 1991). ("Species account for blackside dace (Chrosomus cumberlandensis)", 1991)
Blackside dace spawn from April through June, but the majority of spawning occurs during May (Starnes and Starnes, 1981). During spawning, males develop tubercles and both males and females develop brilliant colors (Etnier and Starnes, 1993). Spawning typically occurs over silt-free gravel in the nests of other cyprinid fish, but presumably riffle areas are used when these nests are not present (Etnier and Starnes, 1993). Females deposit an average of 1,540 ova during spawning (O’Bara, 1985). (Etnier and Starnes, 1993; O'Bara, 1985; Starnes and Starnes, 1981)
Little is known about parental investment in blackside dace. Once the eggs are fertilized and deposited, there is no further parental involvement.
The lifespan of blackside dace is approximately 3 years (Etnier and Starnes, 1993).
Little is known about the behavior of blackside dace.
Blackside dace are presumed to have a small home range. According to Detar, Jones, and Mattingly (2003), most of the 864 dace tagged with an elastomer injection stayed within the original site of capture with the exception of a few individuals migrating 600 to 1800 meters from the capture site and one individual with intertributary movement. (Detar, et al., 2003)
Blackside dace use vision, hearing and chemoreception. In addition, they use their lateral line system to detect vibrations in the water, which may help them avoid predators (Helfman et al., 1997).
Little is known about intraspecific communication in blackside dace. (Helfman, et al., 1997)
Blackside dace feed on algae attached on the stream substrate and potentially beneath banks of the stream (Etnier and Starnes, 1993). According to Etnier and Starnes (1993) blackside dace feed on insect larvae during the winter when algae is less abundant. (Etnier and Starnes, 1993)
Jones and Mattingly (2003) have noted a negative correlation between blackside dace and both redbreast sunfish and largemouth bass abundance that may be due to a predator-prey interaction. (Jones and Mattingly, 2003)
Blackside dace are primary consumers, feeding mainly on algae. They serve as a food source for carnivores, particularly larger fishes, and may occasionally themselves be predators on aquatic insect larvae (USFWS, 1991). ("Species account for blackside dace (Chrosomus cumberlandensis)", 1991)
Blackside dace have no economic value to humans.
Mineral extraction is negatively impacted economically because mining companies cannot disturb streams containing blackside dace, which are then designated as Outstanding Resource Waters. ("NatureServe", 2005)
Blackside dace are listed by the United States Fish and Wildlife Services as Threatened, and are protected under the Endangered Species Act.
Habitat degradation caused by strip mining and logging practices seem to be the leading cause of the decline in numbers of blackside dace. Blackside dace occur in the coalfields of southeastern Kentucky and inhabit headwater streams where these activities have the most impact.
Through the pre-mine permitting process, state and federal agencies restrict or highly regulate mining activities that are to occur in watersheds containing blackside dace.
Mary Hejna (editor), University of Michigan-Ann Arbor.
Chris Isaac (author), Eastern Kentucky University, Sherry Harrel (editor, instructor), Eastern Kentucky University.
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.
Referring to an animal that lives on or near the bottom of a body of water. Also an aquatic biome consisting of the ocean bottom below the pelagic and coastal zones. Bottom habitats in the very deepest oceans (below 9000 m) are sometimes referred to as the abyssal zone. see also oceanic vent.
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.
uses smells or other chemicals to communicate
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
fertilization takes place outside the female's body
union of egg and spermatozoan
forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.
mainly lives in water that is not salty.
An animal that eats mainly plants or parts of plants.
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.
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).
having the capacity to move from one place to another.
specialized for swimming
the area in which the animal is naturally found, the region in which it is endemic.
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
breeding is confined to a particular season
remains in the same area
reproduction that includes combining the genetic contribution of two individuals, a male and a female
associates with others of its species; forms social groups.
uses touch to communicate
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).
The term is used in the 1994 IUCN Red List of Threatened Animals to refer collectively to species categorized as Endangered (E), Vulnerable (V), Rare (R), Indeterminate (I), or Insufficiently Known (K) and in the 1996 IUCN Red List of Threatened Animals to refer collectively to species categorized as Critically Endangered (CR), Endangered (EN), or Vulnerable (VU).
movements of a hard surface that are produced by animals as signals to others
uses sight to communicate
2005. "NatureServe" (On-line). NatureServe Explorer: An online encyclopedia of life. Accessed August 30, 2005 at http://www.natureserve.org/explorer/servlet/NatureServe?searchName=Phoxinus+cumberlandensis.
U. S. Fish and Wildlife Service. 1991. "Species account for blackside dace (Chrosomus cumberlandensis)" (On-line). Endangered and Threatened Species of the Southeastern United States (The Red Book) FWS Region 4. Accessed September 06, 2006 at http://www.fws.gov/endangered/i/e/sae2g.html.
Biggins, R. 1988. Blackside Dace Recovery Plan. Atlanta, GA: U.S. Fish and Wildlife Service.
Detar, J., B. Jones, H. Mattingly. 2003. Factors affecting the distribution and recovery of the threatened blackside dace in Kentucky and Tennessee. Cookeville, TN: Tennessee Technological University.
Etnier, D., W. Starnes. 1993. The Fishes of Tennessee. Knoxville, TN: University of Tennessee Press.
Helfman, G., B. Collette, D. Facey. 1997. The Diversity of Fishes. Malden, MA: Blackwell Science, Inc..
Jones, B., H. Mattingly. 2003. "Building a predictive habitat model for the blackside dace, Phoxinus cumberlandensis" (On-line). Accessed November 01, 2005 at http://www.forestry.caf.wvu.edu/wvuafs/Colloquium/Post-web/abstracts.htm.
O'Bara, C. 1985. Status survey of the blackside dace Chrosomus cumberlandensis . Asheville, NC: U.S. Fish and Wildlife Service.
Starnes, W., L. Starnes. 1981. Biology of the blackside dace Chrosomus cumberlandensis . American Midland Naturalist, 106: 360-370.