Hypophthalmichthys molitrix (Valenciennes in Cuvier and Valenciennes, 1844)

Common Name: Silver Carp

Synonyms and Other Names:

Leuciscus molitrix Valenciennes, 1844  



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Identification: The silver carp is a deep-bodied fish that is laterally compressed.  They are a very silvery in color when young and when they get older they fade from a greenish color on the back to silver on the belly. They have very tiny scales on their body but the head and the opercles are scaleless. They have a large mouth without any teeth in the jaw, but they have pharyngeal teeth. Its eyes are situated far forward on the midline of the body and are slightly turned down.

Silver carp are unlikely to be confused with native cyprinids due to size and unusual position of the eye. They are most similar to bighead carp (H. nobilis) but have a smaller head, and upturned mouth without teeth, a keel that extends forward past pelvic fin base, lack the dark blotches characteristic of bighead carp and have highly branched gill rakers.

Juvenile fish lack spines in fins.  Metalarvae and early juvenile are similar to bighead carp (Hypophthalmichthys nobilis) but pectoral fin extends only to base of pelvic fin (as opposed to beyond in the pelvic fin in bighead)

The species is known for leaping out of the water when startled (e.g., by noises such as a boat motor).

Distinguishing characteristics were given in Berg (1949). Keys that include this species and photographs or illustrations are provided in several of the more recently published state and regional fish books (e.g., Robison and Buchanan 1988; Etnier and Starnes 1993; Pflieger 1997).


Size: 1 m and 27 kg.


Native Range: Several major Pacific drainages in eastern Asia from the Amur River of far eastern Russia south through much of eastern half of China to Pearl River, possibly including northern Vietnam (Berg 1949; Li and Fang 1990).


Great Lakes Nonindigenous Occurrences: This species has been recorded from the Black Warrior and Tallapoosa river drainages of the Mobile Basin, including Yates Reservoir and throughout the central part of Alabama (Mettee et al. 1996; J. Hornsby and M. Pierson, personal communication; Rasmussen 1998); and from the Arkansas and White River systems (including the the lower Cache River), the Ouachita River, Bayou Meto Drainage, and the Mississippi River mainstem in Arkansas (Freeze and Henderson 1982; Carter and Beadles 1983; Courtenay et al. 1984; Robison and Buchanan 1988). It has been stocked in water treatment ponds on the East Slope of Colorado (D. Horak, personal communication).  A specimen was collected in power plant reservoir in Larimer Co.; plant is on Rawhide Creek; a trib of the Cache la Poudre River (Walker, unpublished).  It has been intentionally released in Hawaii (Davidson et al. 1992). It has also been collected or reported from several water bodies in, or bordering, Illinois, including the Mississippi, Spoon, Illinois, and Ohio rivers and several of their tributaries, the Muddy River, Muscooten Bay, Horseshoe Lake and vicinity in the Cache River drainage (Burr 1991; Burr et al. 1996; Laird and Page 1996; Illinois Natural History Survey 2004; Hoff, pers. comm.; Etnier, pers. comm.; Thomas, pers. comm.; Irons, pers. comm.; Southern Illinois University, unpublished) and the Embarras River below Lake Charleston (K. Cummings, personal communication). There are also records of this species from the southeastern part of Indiana (presumably the Ohio River) (Courtenay et al. 1991; Simon et al. 1992) and west fork of the White River in Greene County (Indiana Dept. of Natural Resources 2003); the Des Moines and Chariton Rivers, Iowa (Iowa DNR 2003), White River at Hazelton (Caskey, pers. comm.) and the Wabash River (Thomas, pers. comm.); eastern rivers in Kansas and some unspecified location(s) in Kansas (Rasmussen 1998; Courtenay et al. 1991) (possibly the Missouri River); from the Ohio River, Clarks River, and non-specific locations in Kentucky (Pearson and Krumholz 1984; Burr and Warren 1986; Rasmussen 1998; Thomas, pers. comm.; Henley, pers. comm.; Southern Illinois University; Baxter, pers. comm.); from the lower Mississippi River and many tributary sites in Louisiana including the Atchafalaya, Red, Boeuf, Old, Ouachita, and Little river drainages, LaFourche Canal, Miller Lake, and Loggy Bayou (Freeze and Henderson 1982; Carp Task Force 1989; Douglas et al. 1996; Rasmussen 1998; F. Bryan and J. Hughes Little, pers. comm.); the Mississippi River, Yazoo River, and Chotard Lake in Mississippi (Mississippi Museum of Natural Science 2004; Schramm et al. 2004);  from the Mississippi and Missouri river mainstems and the Lamine and Castor Rivers, Missouri (Courtenay et al. 1991; Robinson 1995; Pflieger 1997; Rasmussen 1998; Lien 2003), the Little River Ditches, Upper Mississippi-Cape Girardeau, and The Sny drainages (Southern Illinois University), the Lower Missouri-Moreau, Lower Grand, Lamine, Lower Osage drainages (Chapman, pers. comm.); the Missouri River drainage and Elkhorn River Nebraska (Nebraska Game and Parks 2000) and established in Boyer Chute National Wildlife Refuge (USFWS 2005); the Missouri River up to Gavins Point Dam (W. Stancill, pers. comm.), the Big Sioux River near Canton (T. St. Sauver, pers. comm.), the Vermillion River (Hayer et al. 2014), and the mouth of the James River (R. Klumb, pers. comm.) in South Dakota. They also have been collected from a Mississippi River outflow in Tennessee (C. Saylor, personal communication; Etnier, pers. comm.) and McKellar Lake in Memphis (Baxter, pers. comm.).

This species has also been collected at golf course ponds at Dorado Beach Hotel in Puerto Rico (Erdman 1984).


Table 1. Great Lakes region nonindigenous occurrences, the earliest and latest observations in each state/province, and the tally and names of HUCs with observations†. Names and dates are hyperlinked to their relevant specimen records. The list of references for all nonindigenous occurrences of Hypophthalmichthys molitrix are found here.

Full list of USGS occurrences

State/ProvinceFirst ObservedLast ObservedTotal HUCs with observations†HUCs with observations†
IL202220221Little Calumet-Galien

Table last updated 11/12/2024

† Populations may not be currently present.


Ecology: Silver carp are primarily a species of large rivers.  They can tolerate salinities up to 12 ppt and low dissolved oxygen (3mg/L).  Silver carp feed on both phytoplankton and zooplankton (Radke and Kahl 2002).

In their native range, silver carp reach maturity at between 4 and 8 years old but are noted in North America to mature as early as just 2 years old.  They can live to 20 years.  Spawning occurs at temperatures greater than 18oC.  A mature female can lay up to 5 million eggs per year.  Eggs require current to stay suspended, with a minimum length of spawning river estimated at 100km and a current speed of 70cm/s.


Great Lakes Means of Introduction: This species was imported and stocked for phytoplankton control in eutrophic water bodies (Kelly et al. 2011). The first import into the United States occurred in 1973 when a private fish farmer imported silver carp into Arkansas (Freeze and Henderson 1982). By the mid 1970s, the rearing of silver carp was expanded to six state, federal, and private facilities after being stocked in several municipal sewage lagoons (Robison and Buchanan 1988). By 1980, the species was discovered in natural waters, probably a result of escapes from fish hatcheries and other types of aquaculture facilities (Freeze and Henderson 1982). Pearson and Krumholz (1984) suggested that individuals taken from the Ohio River may have come from plantings in local ponds or entered the Ohio River from populations originally introduced in Arkansas.


Great Lakes Status: Although silver carp has not been physically detected in the Great Lakes, environmental DNA (eDNA) has been found in water samples collected in several areas in 2012: above electric barriers from Lake Calumet, the Little Calumet River, the North Shore Channel, and the Chicago River (USACE 2012), as well as Maumee Bay, Lake Erie (Jerde et al. 2013). In 2014, a positive silver carp eDNA result was found in the lower Kalamazoo River, just below the Caulkins Dam. However, no silver carp were detected (Michigan Department of Natural Resources 2014).

Hypophthalmichthys molitrix has a moderate probability of introduction to the Great Lakes (Confidence level: High).

Potential pathway(s) of introduction: Dispersal, unauthorized release, escape from commercial culture
Currently, large populations of this species are already established in nearby waters connected to the Great Lakes basin including the Illinois river and the Chicago Area Waterway System (Baerwaldt et al. 2013). On June 22nd, 2017 a 4 year old male silver carp was found nine miles from Lake Michigan in the Little Calumet River of the Chicago Area Waterway System (CAWS). This was the first silver carp collected above the electrical barriers in the CAWS. The autopsy revealed that this fish originated in the Illinois/Middle Mississippi watershed and spent a quarter of its life in the Des Plaines River watershed before being caught and removed from the Little Calumet River. Though it remains unknown how the fish arrived above the electric barriers, the autopsy revealed that the fish spent anywhere from a few weeks to a few months in the stretch of river where it was collected (Asian Carp Regional Coordinating Committee 2017). Prior to this record, the closest location to Lake Michigan at which a silver carp has been collected was in the Des Plaines River (river mile 290.2) at the confluence with the CSSC, north of Joliet, IL and downstream of the electric barriers (USGS 2013).

Live silver carp are sometimes available in live food fish markets in several major U.S. and Canadian cities, including Toronto (Kolar et al. 2005).


Hypophthalmichthys molitrix has a moderate probability of establishment if introduced to the Great Lakes (Confidence level: High).

The silver carp has unique, sponge-like and porous gill rakers capable of straining phytoplankton down to 4 microns in diameter (Robison and Buchanan 1988). They can feed in temperatures as low as 2.5°C (36.5°F) and can withstand low levels of oxygen (Pennsylvania Sea Grant 2013). It would be highly likely for the silver carp to find an appropriate food source but the amount they eat might not be sufficiently found in the Great Lakes. Recent bioenergetics modeling efforts suggest that plankton concentrations could support silver carp growth in productive nearshore areas and embayments (e.g. Green Bay and the Western Basin of Lake Erie), but the fish would likely be food-limited in the oligotrophic offshore regions (Cooke and Hill 2010; Anderson et al. 2015; Anderson et al. 2017).

Kolar et al. (2007) stated that the limiting factor for invasive carp establishment in most regions of the United States would be access to a river in which invasive carp could successfully spawn. Several studies have found that there are several Great Lakes tributaries that have the necessary hydrologic characteristics and temperature regimes to support successful spawning (Kocovosky et al. 2012; Murphy and Jackson 2013; Chapman et al. 2013). Additionally, Cuddington et al. (2014) suggests that establishment would be likely for a small number of founding individuals (<20 fish) despite environmental stochasticity. Furthermore, the presence of only a few suitable spawning rivers on each lake may promote the establishment success given that silver carp would have an increased chance of finding a mate due to the fish aggregating in the relatively few nearby spawning rivers. However, establishment becomes less likely if age of first sexual reproduction is substantially delayed.


Great Lakes Impacts:
Summary of species impacts derived from literature review. Click on an icon to find out more...

EnvironmentalSocioeconomicBeneficial



Hypophthalmichthys molitrix has a high potential socio-economic impact in the Great Lakes.
Silver carp's tendency to leap out of the water, especially when encountering outboard motors, has had a significant negative impact on the recreational and tourism sectors, resulting in collisions with boaters, injuries to humans, and damage to boats and equipment. These jumps, reaching heights of at least 10 feet, have caused severe injuries to boaters, raising concerns that collisions with jumping silver carp may eventually lead to human fatalities (USFWS, 2006; Hoff, 2004).

Silver carp are carriers of disease-causing agents, posing health risks to humans, particularly in different parts of Iran. These pathogens include Listeria monocytogenes (found in market and fish farm samples), Clostridium botulinum (present in 1.1% of fresh and smoked samples from the Mazandaran Province), and toxigenic fungi such as Aspergillus flavus, Alternaria, Penicillium, and Fusarium (detected in silver carp and the pond water where they were raised). Additionally, silver carp may serve as a potential carrier of Salmonella (S. typhimumium) (USFWS, 2006).

These fish compete with native species that are important as sport and food species and whose decline could result in a negative economic impact on recreational angling and other industries that benefit from sport fishing, such as tourism (Kolar et al. 2005).

Hypophthalmichthys molitrix has a high potential environmental impact in the Great Lakes.
The silver carp is a filter-feeder capable of consuming large amounts of phytoplankton, zooplankton, bacteria, and detritus (Leventer 1987). Silver carp, as efficient filter feeders, engage in interspecific competition with various fish species during their early life stages, potentially leading to declines in the physical condition and long-term sustainability of native fish when plankton resources are limited (Chick and Pegg, 2001; Irons et al., 2007). Studies indicate that their superior filter efficiency and large size can disproportionately deplete plankton, alter zooplankton communities, and modify food web structure (Domaizon and Devaux, 1999; Spataru and Gophen, 1985; Starling, 1993; Irons et al., 2007; Pongruktham et al., 2010). Furthermore, Silver carp can impact water quality by excreting substantial amounts of nutrients, leading to increases in inorganic nitrogen and phosphorus levels, changes in zooplankton populations, and subsequent increases in chlorophyll a and turbidity (Herodek et al., Starling, 1993; Lieberman, 1996).

Another concern is the presence of the Asian tapeworm, which has been found in silver carp populations and poses a risk of transmission to other fish species, causing severe intestinal damage (Kolar et al., 2007; Conover et al., 2007). This parasite has also been detected in several native North American fish species, including endangered species (Kolar et al., 2005).

Hypophthalmichthys molitrix has the potential for high beneficial effects if introduced to the Great Lakes.
Silver carp holds significant commercial value worldwide, with China being a particularly important producer. In the US, commercial harvest of silver carp is increasing in certain regions of the Mississippi River Basin, and there is ongoing investigation into developing a consumer market for invasive carp species, along with the emergence of fishing tournaments targeting silver carp (Kolar, 2005; Conover et al., 2007). These fish are often studied for biomanipulation purposes in wastewater treatment and eutrophic lakes, but conflicting results have been observed regarding their effectiveness in controlling plankton blooms and improving water quality (Domaizon and Devaux, 1999b; Henderson, 1978; Spataru and Gophen, 1985; Starling, 1993). Similarly, debates persist about the ability of silver carp to control cyanobacteria blooms, with some studies suggesting their consumption of blue-green algae while others indicate potential increases in blue-green algae and overall phytoplankton populations (Xie et al., 2004; Kolar et al., 2005).


Remarks: Jenkins and Burkhead (1994) reported on the use of silver carp in a wastewater treatment pond in the upper James River drainage of Virginia. However, there is as yet no record of the species in Virginia open waters. One of the so-called Invasive Carps, the silver carp is a filter-feeder capable of taking large amounts of phytoplankton. Its diet also includes zooplankton, bacteria, and detritus (Leventer 1987). This species has been intensively cultured in many parts of the world, often raised in combination with other fishes.

The report in Fuller et al. (1999) from Bay County, Florida was actually a bighead carp (UF 98162).

Voucher specimens: Illinois (SIUC 17716, 23043, 23046, 24415; INHS 88425); Louisiana (NLU 65811, 66858, 66859).


References (click for full reference list)


Author: Nico, L., G. Nunez, E. Baker, P. Alsip, and J. Redinger


Contributing Agencies:
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Revision Date: 5/31/2024


Peer Review Date: 1/22/2015


Citation for this information:
Nico, L., G. Nunez, E. Baker, P. Alsip, and J. Redinger, 2024, Hypophthalmichthys molitrix (Valenciennes in Cuvier and Valenciennes, 1844): U.S. Geological Survey, Nonindigenous Aquatic Species Database, Gainesville, FL, and NOAA Great Lakes Aquatic Nonindigenous Species Information System, Ann Arbor, MI, https://nas.er.usgs.gov/queries/greatlakes/FactSheet.aspx?Species_ID=549, Revision Date: 5/31/2024, Peer Review Date: 1/22/2015, Access Date: 11/12/2024

This information is preliminary or provisional and is subject to revision. It is being provided to meet the need for timely best science. The information has not received final approval by the U.S. Geological Survey (USGS) and is provided on the condition that neither the USGS nor the U.S. Government shall be held liable for any damages resulting from the authorized or unauthorized use of the information.