Pacifastacus leniusculus (Dana, 1852)

Common Name: Signal Crayfish

Synonyms and Other Names:

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Identification: The dorsal surface of Signal Crayfish is typically brownish-tan in coloration. Although most individuals of Pacifastacus leniusculus conform to this, coloration may be highly variable based on locality and can range from bright red to blue in some cases (Larson and Olden 2011). A bright red coloration on the underside of claws, and a white or turquoise colored patch present at the base of each claw joint is distinctive to the Signal Crayfish (Riegel 1959; Larson and Olden 2011). Additionally, the surface of the carapace and claws are smooth, lacking the pronounced bumps that are typical of other nonnative crayfish (Orconectes rusticus and O. virilis) introduced to the Pacific Northwest (Larson and Olden 2011). Signal Crayfish can be distinguished from the White Claw Crayfish (Austropotamobius pallipes) in Europe by the absence of spines along the cervical groove (margin between the head and body) (Pöckl et al. 2006).

Pacifastacus leniusculus (Dana, 1852), which is part of the subgenus Pacifastacus, is divided into three subspecies; leniusculus, klamathensis (Stimpson, 1857), and trowbridgii (Stimpson, 1857). Initially described as separate species, the similar, yet highly variable morphology shared by these subspecies has challenged taxonomists for decades (Larson et al. 2012). Miller (1960) was the first to describe these as subspecies of P. leniusculus. Genetic studies have since identified P. l. leniusculus and P. l. trowbridgii as being the most similar of the three subspecies, while P. l. klamathensis is the most distinct (Agerberg and Jansson 1995

Physical features key in differentiating P. l. leniusculus from P. l. trowbridgii include the presence of sharp spines on the post orbital ridge and a relatively narrow carapace. In contrast, P. l. trowbridgii typically have a robust carapace with rounded tubercles on their post orbital ridge. Small tubercles rather than spines are present in P. l. klamathensis’ post orbital ridge, and the white to blue-green pigmentation commonly found on the chelae of the other subspecies is often absent. Additionally, the rostrum of P. l. klamathensis is very wide relative to the length of its acumen (Riegel 1959; Miller 1960; Larson and Williams 2015). Due to the difficulty and complexity of distinguishing these subspecies, Larson et al. (2012) summarized Miller’s (1960) identifying criteria (Larson et al. 2012 - appendix S1). The characteristics summarized by Larson et al. (2012) are illustrated in the table below for comparisons.

Summarized identifying characteristics of Signal Crayfish subspecies (Larson et al. 2012).
  Signal Crayfish
P. l. leniusculus
Columbia River Signal Crayfish
P. l. trowbridgii
Klamath Signal Crayfish
P. l. klamathensis
Claws (chelae) Wide with long finger, short and highly convex palm Wide with intermediate finger appendage, and palm slightly to greatly convex Wide with intermediate finger length and palm slightly to greatly convex
Acumen length Long relative to width at rostral spines Intermediate relative to width at rostral spines Short relative to width at rostral spines
Sides of rostrum Strongly converging Converging to nearly parallel Converging to nearly parallel
Rostrum length Long relative to total carapace length Long relative to total carapace length Short relative to total carapace length
Post orbital spines Long Short or tubercle-like Short or tubercle-like
Areola length Short relative to total length Intermediate relative to total length Intermediate relative to total length
Head (cephalon) length Long Intermediate relative to total length Intermediate relative to total length
Carapace Cylindrical (narrow relative to orbital carapace length) Wide relative to orbital carapace length Wide relative to orbital carapace length

 


Size: The average Signal Crayfish attains a carapace length (CL) of 50-70 mm (Capurro et al. 2007).


Native Range: Pacifastacus leniusculus is a wide-ranging species native to the Northwestern United States (Larson and Olden 2011). Much of the Signal Crayfish’s presumed native range is found within the Columbia River Basin. From the Columbia River’s lower estuary, the native range spans northwest up the mainstem to tributaries that reach into Washington, Oregon, Idaho, and British Columbia. The native range extends south from the Columbia River along Oregon’s coast where the Klamath River and its drainages form its southern boundary (Miller 1960; Larson et al. 2012).

The subspecies of Signal Crayfish are believed to have once been geographically isolated populations (Hobbs 1988). Mixing due to the prevalence of early introductions, a lack of historical records, and hybridization between subspecies has made describing their native range and taxonomic status problematic (Hobbs 1988; Lowery and Holdich 1988; Larson and Williams 2015). This has led the subspecies of Signal Crayfish to be commonly regarded as a single species (Hobbs 1988). Genetic tests have begun to shed light on this, but the extent of the native distributions of Signal Crayfish subspecies continues to be a contested subject (Larson and Williams 2015).

The subspecies P. l. leniusculus, is believed to be native to the lower Columbia River and its tributaries (including the Willamette River) in western Oregon and Washington state. It is also assumed to be native to the Umpqua River, which is believed to have had a historic drainage connection to the Willamette (Miller 1960; Larson and Williams 2015). Based on Miller’s (1960) accounts, it is probable that Pacifastacus leniusculus trowbridgii is also native to the lower Columbia River basin, and nearby coastal rivers, such as the Umpqua, which were likely once connected via stream capture (Miller 1960; Larson et al. 2012; Larson and Williams 2015). Pacifastacus leniusculus klamathensis is presumed to be native to the Klamath River in Northern California and Southern Oregon, but the extent of its native range beyond this basin is unknown due to decades of introductions that have resulted in the mixing of populations.


Ecology: Pacifastacus leniusculus typically seek shelter in rocky crevices or woody debris within streambeds and littoral zones (Holdich and Lowery 1988). The signal crayfish is considered a non-burrowing crayfish (Shimizu and Goldman 1983), although they are known to construct shallow borrows. Burrowing activity is most common in crayfish smaller than 50 mm and the least common in larger males (Guan 2010). The population density of Signal Crayfish is correlated with refugee availability (Flint 1975), and waterbodies with rocky littoral zones support far greater densities than places with clay banks (Shimizu and Goldman 1983).

The Signal Crayfish occupies a range of habitats throughout its native and non-native distribution (Goldman and Rundquist 1977; Holdich and lowery 1988). Though P. leniusculus prefers low gradient streams typical of agricultural low-lands in western Oregon (Avault 1973), they inhabit both coastal and upland streams, lakes, and rivers (Lowery and Holdich 1988). Signal crayfish can be found in habitats ranging from clear, shallow coastal streams (Lowery and Holdich 1988), to major rivers with high turbidity (Ibbotson and Furse 1995), as well as eutrophic and oligotrophic lakes and reservoirs (Holdich and Lowery 1988). Pacifastacus leniusculus also occupies the saline and often turbid waters of major river deltas (Shimizu and Goldman 1983). Wheatly & McMahon (1983) revealed via a laboratory study that Signal Crayfish can occupy waterways with salinity as high as ~26 ppt (75% seawater), for several days. Additionally, Miller (1965) noted that Signal Crayfish have been observed copulating, molting, and laying eggs in brackish water.

The breeding cycle of the Signal Crayfish follows that of most temperate zone crayfish. Copulation occurs during the autumn months (September or October), and females carry the eggs throughout the winter (Holdich and Lowery 1988). Eggs then typically hatch in March and April as the water warms (Shimizu and Goldman 1983). The young from populations residing in cooler waters may hatch later in the year (June and July), since growth is temperature dependent. Once hatched, P. leniusculus grow rapidly and most individuals mature during their second summer. The time to maturity may also be delayed by cooler water temperatures, such as that of Lake Tahoe. Here, males may mature during their third summer, while females may not mature until fourth (Holdich and Lowery 1988). Abrahamsson and Goldman (1970) estimated that male and female P. leniusculus in the Sacramento River, CA., mature when they reach the size of 29-37 mm CL and 25-35 mm CL, respectively. Crayfish growth is also density dependent, which often results in small, newly established populations of P. leniusculus experiencing a short period of rapid growth (Hogger 1986).

Pacifastacus leniusculus is both a fast growing and long-lived species. It’s known as one of the fastest growing species of temperate zone crayfish (Holdich and Lowery 1988), and in general, the highest growth rates are associated with populations which have recently invaded an unexploited habitat (Hogger 1986). These rapid growth rates subside as populations establish and densities surge, presumably because of increased competition for food and space (Hogger 1986). Their potential for rapid growth has made them the focus of both aquaculture productions and commercial fisheries in several countries (Westman 1973; Furst 1977; McGriff 1983; Goddard and Hogger 1986; Lowery and Holdich 1988). Hogger (1984) found that individuals from a population of P. leniusculus in southern England had the potential to grow up to 62 mm CL in as few as three years when grown in ideal conditions.  Overall, the Signal Crayfish may survive up to 9 years or more when living in the wild (Goldman and Rundquist 1977).


Means of Introduction: Potential introduction pathways for P. leniusculus include stocking for harvest, the release of crayfish used as live bait, and stocking as an additional food source for fish (Lowery and Holdich 1988; Lodge et al. 2000). The Signal Crayfish is known to be introduced to the Truckee River and Lake Tahoe, NV., as early as 1895 and 1909, respectively (La Rivers 1962; Abrahamsson and Goldman 1970), and records show that it was stocked in the Sacramento River and coastal waterways of California as early as 1912 (Riegel 1959). In both regions, P. leniusculus was intentionally stocked to enhance the forage available to fish (both native and nonnative), and to provide a harvest fishery for residents (La Rivers 1962; Abrahamsson and Goldman 1970; Lowery and Holdich 1988, lodge et al. 2000).


Status: Human mediated introductions have allowed Signal Crayfish (P. l. leniusculus, P. l. klamathensis, and P. l. trowbridgii) to expand their distributions into a variety of habitats ranging from the warm coastal waterways of the Sacramento River Delta to the sub-alpine waters of Lake Tahoe and Donner in California (Holdich and Lowery 1988; Larson et al. 2012; Larson and Williams 2015). The Signal Crayfish (Pacfastacus l. leniusculus) has been introduced to and is established in regions of Oregon, Washington, California, Nevada, Utah, and British Columbia. The Columbia River Signal Crayfish (Pacifastacus l. trowbridgii) is also known to be established in regions outside of its native range in Oregon, Washington, California and Nevada (Taylor et al. 2007). Based on the invasion history, it is likely that the distributions of P. leniusculus subspecies have been augmented within their own proposed native ranges through additional stockings (Larson and Olden 2011). For example, Signal Crayfish in Crater Lake, OR., were historically restricted from entering the waterbody, but later stocked there in 1915 to provide food for game fish previously introduced to the lake (Lowery and Holdich 1988; Girdner 2018).  Pacifastacus leniusculus is now so abundant in California it supports a robust commercial fishery in the Sacramento River Delta (McGriff 1983).


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

EnvironmentalSocioeconomicBeneficial



Pacifastacus leniusculus has the potential for High environmental impact if introduced to the Great Lakes.
    Signal Crayfish are a known carrier of Crayfish plague, a parasite listed as one of the top 100 worst invaders by the International Union for Conservation of Nature (Lowe et al., 2000). Crayfish Plague spread by Signal Crayfish was a major contributor to declines in native Noble Crayfish populations throughout Europe (Alderman, 1996). P. leniusculus are opportunistic polytrophic feeders which affect populations of fish, macroinvertebrates, and aquatic plants through competition and predation (Guan & Wiles 1997; Nyström 1999; Lewis 2002). Griffiths et al. (2004) found that Signal Crayfish outcompeted Atlantic Salmon for shelter in an artificial test arena, possibly indicating that their presence might make sport fish more vulnerable to predation. Although they are not known to burrow in their native range, P. leniusculus construct burrows that contribute to bank erosion and collapse in their introduced range (GISD, 2005).

Pacifastacus leniusculus has the potential for moderate Socio-Economic impact if introduced to the Great Lakes.
Signal Crayfish have not been reported to present any hazards to human health or infrastructure. They have not been shown to diminish water quality or inhibit recreational use significantly. However, their presence may affect Atlantic Salmon fisheries through shelter competition (Griffiths et al., 2004) and consumption of eggs (Findlay et al. 2014). Signal Crayfish burrows reach a high density which could potentially reduce the perceived aesthetic of the areas it inhabits.
      
Pacifastacus leniusculus has the potential for high beneficial impact if introduced to the Great Lakes.
    Signal Crayfish are a popular species for bait as well as human consumption. They are commonly used to control nuisance vegetation in aquaculture ponds (GISD, 2005). They are commercially valuable both for aquaculture and as a fishery, they are commercially harvested in the western US as well as in Europe (GISD, 2005).


Remarks: The Signal Crayfish’s ability to exploit a variety of habitats and conditions has enabled it to become established in a wide range of environments throughout Europe (Lowery and Holdich 1988). During the late 19th and early 20th centuries, crayfish in many European countries were decimated by the fungal infection, Aphanomyces astaci, also known as the crayfish plague (Alderman et al. 1996).  The collapse of Noble Crayfish (Astacus astacus) populations in the late 19th and early 20th century greatly impacted European countries, such as Sweden, where crayfish supported significant commercial fisheries (Lowery and Holdich 1988). Beginning in the 1960’s, Pacifastacus leniusculus were imported to Sweden and introduced throughout Europe in an attempt to establish a plague resistant species that would supplement stocks decimated by the crayfish plague. The Signal Crayfish is now widespread throughout Europe where it supports commercial fisheries but threatens endemic species such as the Noble Crayfish (Astacus astacus) through competition and disease (Lowery and Holdich 1988; Ibbotson and Furse 1995, Holdich et al. 2009).


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Author: Procopio, J.


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Revision Date: 9/14/2021


Citation for this information:
Procopio, J., 2024, Pacifastacus leniusculus (Dana, 1852): 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=200, Revision Date: 9/14/2021, Access Date: 5/2/2024

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.