Regulations | Jurisdiction | Regulation | Law | Description | Date Effective |
| United States | Prohibited | Lacey Act (18 U.S.C. 42) | In the United States and its territories, the importation or transportation of this species is prohibited unless otherwise stated. | 12/1/2020 |
| Illinois | Prohibited | 17 Ill. Adm. Code Ch. I, Sec. 805 | This species is listed as injurious in Illinois and shall not be possessed, propagated, bought, sold, bartered or offered to be bought, sold, bartered, transported, traded, transferred or loaned to any other person or institution unless a permit is first obtained. | 5/18/2015 |
| Michigan | Prohibited | Natural Resources Environmental Protection Act (Part 413 of Act 451) | It is prohibited in Michigan and is unlawful to possess, introduce, import, sell or offer this species for sale as a live organism, except under certain circumstances. | 3/21/2019 |
| Minnesota | Prohibited | Statute 84D.07 | This species is prohibited in Minnesota and is unlawful (a misdemeanor) to possess, import, purchase, transport, or introduce this species except under a permit for disposal, control, research, or education. | 1/1/2020 |
| Ohio | Prohibited | Ohio Administrative Code 1501:31-19-01 | In Ohio, it shall be unlawful for any person to possess, import or sell live individuals of this species. | 7/1/2016 |
| Wisconsin | Prohibtied | Chapter NR 40, Wis. Adm. Code | All species of the family Parastacidae are prohibited in Wisconsin and one cannot transport, possess, transfer, or introduce it without a permit. | 4/1/2017 |
| Ontario | Prohibited | Invasive Species Act, 2015, S.O. 2015, c. 22 - Bill 37 | It is prohibited in Ontario, making it illegal to import, possess, deposit, release, transport, breed/grow, buy, sell, lease or trade this species. | 11/3/2015 |
| Quebec | Restricted | SOR/90-214 | In Quebec, this species cannot be used as bait. | 6/1/2021 |
Note: Check federal, state/provincial, and local regulations for the most up-to-date information.
Control
Biological
If C. destructor were to become established in the Great Lakes basin, populations might be controlled by predatory fish. Eels, burbot, perch, pike, and smallmouth bass are some well-known predators of crayfish that exist in the Great Lakes (Westman 1991 in Gherardi et al. 2011). One study observed in a mesocosm experiment that northern pike (Esox lucius) were an efficient predator of crayfish independent of prey size (Neveu 2001 in Gherardi et al. 2011), which could be significant considering the large size of C. destructor. Fish predation could be effective in managing C. destructor, but some studies have suggested that stocking predacious fish could actually increase non-indigenous crayfish species population densities (Gowing and Momot 1979, and Holdich and Domaniewski 1995 in Gherardi et al. 2011). Predatory aquatic birds, such as cormorants, herons, and ibis are predators of C. destructor and all exist in the Great Lakes region (Farrell and Leonard 2001).
The use of microbial agents to control crayfish populations has been reviewed in previous studies (Gherardi et al. 2011; Scalici et al. 2009). C. destructor is known to be susceptible to the crayfish plague, Aphanomyces astaci (Scalici et al. 2009), of which North American species are much more resistant (Persson et al. 1987; Unestam 1975). Four populations of C. destructor in Spain were eradicated by introducing signal crayfish (Pacifastacus leniusculus) infected with the plague into the populations (Diéguez-Uribeondo and Muzquiz 2005 in Peay 2009). The crayfish plague was responsible for the eradication of C. destructor in the Laghi di Ninfa Natural Reserve, Italy. The disease was brought to the area by another invasive crayfish, Procambarus clarkii (Mazza et al. 2018). P. clarkii is already present and spreading in the Great Lakes region. C. destructor is also susceptible to the microsporidian disease, Thelohania parastaci (Moodie et al. 2003) and the Cherax destructor systemic parvo-like virus (CdSPV) (Edgerton 1996, Edgerton et al. 1997 in Diggles 2011). Gherardi et al. (2011) mentions that the use of genetically modified strains of A. astaci has been hypothesized as a potential way to control invasive crayfish in Europe, but there is a significant risk that using a genetically modified strain in conjunction with the existing wild-type could affect more than just the target species. The use of microbial agents as a method of control for C. destructor in the Great Lakes basin would also warrant the consideration of indirect effects on native crayfish populations.
Aside from predatory fish and disease, other potential methods of control would be the use of sex pheromones or the release of sterile males. Aquiloni and Gherardi (2010) observed the capability of sex pheromones as a method of control in another species of crayfish, which could have implications for the control of C. destructor if it becomes established in the Great Lakes. Additionally, the release of sterile male C. destructor into a population could be an effective method of control if the species were to become established within the Great Lakes basin. The sterile male release technique is species-specific and has been tested for other species of invasive crayfish in laboratory settings (Aquiloni et al. 2009).
Chemical
The use of chemical agents to control C. destructor populations has been examined by Gherardi et al. (2011) and the New South Wales Department of Primary Industries (2017). In particular, the assessments of insecticides as a possible control of crayfish populations could provide insight on the viability of this control method for C. destructor. C. destructor is susceptible to organochlorines found in some insecticides and herbicides (NSW Department of Primary Industries 2017). Gherardi et al. (2011) noted the success of insecticides derived from natural pyrethrum and synthetic pyrethroids in eradicating crayfish populations in Europe (Gherardi et al. 2011). Organophosphate insecticides (e.g. fenthion and methyl parathion) have also been utilized in attempts to eradicate invasive crayfish species, but these organophosphates apparently lack specificity among crustaceans and insects (Gherardi et al. 2011), so using this control method may harm native species as well as C. destructor. Two insecticides (active ingredients cypermethrin or deltamethrin) were found to be suitable biocides for eradicating crayfish populations. These insecticides are highly toxic to crayfish at low concentrations, have low accumulation rates in the food chain, and do not persist in aquatic environments long-term (Lidova et al. 2019). Other studies have observed the effect surfactants have on controlling crayfish activity, but this method has shown to have a limited effect in the eradication of populations (Cabral et al. 1997 and Fonseca et al. 1997 via Gherardi et al. 2011). Salt can be used as a chemical control in confined settings; C. destructor will die at a salinity of 25 ppt or above (NSW Department of Primary Industries 2017).
Physical
The use of physical barriers and diversions have been reviewed as a method to control non-indigenous crayfish species populations in Europe and America (Gherardi et al. 2011; Kerby et al. 2005). Kerby et al. (2005) observed that red swamp crayfish (Procambarus clarkii) movement was significantly reduced by natural barriers. Other physical control methods include the use of electric fences and vibrations (Gherardi et al. 2011). Mechanical removal of C. destructor could also be a potential control method. Continuous trapping has been demonstrated to work on rusty crayfish (Faxonius rusticus) in a Northern Wisconsin lake (Hein et al. 2007) as well as in aquaculture ponds (Bills and Marking 1988). Gherardi et al. (2011) suggests that electrofishing and trapping could also be an effective way of controlling non-indigenous crayfish species populations.
Note: Check state and local regulations for the most up-to-date information regarding permits for pesticide/herbicide/piscicide/insecticide use.