Invasion History

First Non-native North American Tidal Record: 1985
First Non-native West Coast Tidal Record:
First Non-native East/Gulf Coast Tidal Record: 1985

General Invasion History:

North American Invasion History:


Pterois volitans (Red Lionfish) has an almond-shaped body, and a large head, one-third to one-half body length, with numerous head spines, and often with large tentacles above the eyes. Dorsal fin spines and rays of dorsal, anal, pelvic and pectoral fins are greatly elongated, making the fish look a little like an exploding firework. The caudal fin is rounded. Eleven species of Lionfish (Pterois are known, some very similar morphologically to P. volitans. Pterois miles, very similar to P. volitans, has also been introduced to the the Western Atlantic, and can be distinguished only by meristic counts, morphometrics, and fine morphological details, or molecular methods (Schultz 1986; Hamner et al. 2007; Freshwater er al. 2009; Florida Museum of Natural History 2017; Froese and Pauly 2017; USGS Nonindigenous Aquatic Species Program 2017).

The dorsal fin of Pterois volitans has 13 spines and 9-12 (usually 11) soft rays. The anal fin has 3 spines, and 6-8 (usually 7) soft rays. (For P. miles, the usual numbers are 10 dorsal rays and 6 anal rays). Color patterns vary greatly with environment, but are basically zebra-striped in red and white. The soft dorsal, anal, and caudal fins are spotted. (Pectoral fins and fin spots are smaller in P. miles). The usual maximum size of P. volitans is ~380mm, but one specimen off Venezuela reached 457 mm (Schultz 1986; Ehemann 2017; Florida Museum of Natural History 2017; Froese and Pauly 2017; USGS Nonindigenous Aquatic Species Program 2017).

Of 180 specimens of Western Atlantic Pterois examined at the molecular level by Hamner et al. 2004), 168 were identified as P. volitans, primarily a western Pacific species, 12 specimens as P. miles, whose range encompasses thee wstern tropical/subtropical Indian Ocean (Africa-Red Sea-Australia) (Hamner et al. 2007). For both species, intraspecific variation in color and morphology is greater than that between species (Schultz 1986; Lowe 2016). A dramatic case is the appearance and rapid spread of a an apparently distinct morphoology of the supraoptical tentacle in both species, both in Indo-Pacific and Atlantic populations. The supraoptical tentacle can either be a simple, unbranched tentacle, or have a highly branched 'peacock-feather' morphology. This polymorphism probably evolved before the divergence of the two species (Morris and Freshwater 2008). Recent genetic studies indicate that hybridization has been occurring between P. volitans and P. miles in the Atlanitc, and P. volitans, in its native Indo-Pacific, has undergone genetic exchange with the more localized species P. lunulata (Luna Lionfish) and P. russelli (Plaintail Turkeyfish) (Wilcox et al. 2018). These authors suggest that heterosis ('hybrid vigor') may have contributed to the invasiveness of inttoduced lionfishes.


Taxonomic Tree

Kingdom:   Animalia
Phylum:   Chordata
Subphylum:   Vertebrata
Superclass:   Osteichthyes
Class:   Actinopterygii
Subclass:   Neopterygii
Infraclass:   Teleostei
Superorder:   Acanthopterygii
Order:   Scorpaeniformes
Suborder:   Scorpaenoidei
Family:   Scorpaenidae
Genus:   Pterois
Species:   volitans


Gasterosteus volitans ( Linnaeus, 1758)
Pterois zebra (Quoy and Gaimard, 1825)
Pterois cristatus ( Swainson, 1839)
Pterois volitans castus (Whitley, 1951)

Potentially Misidentified Species

Dendrochirus brachypterus
Shortfin Turkeyfish, Indo-Pacific, also in aquarium trade, not yet found in wild (Lyons et al. 2017)

Dendrochirus zebra
Zebra Turkeyfish, Indo-Pacific, also in aquarium trade, not yet found in wild (Lyons et al. 2017)

Pterois lunulata
Pterois lunulata (Luna Lionfish), a Northwest Pacific native, is closely related to P. volitans (Red Lionfish), eastern Indo-Pacific, and P. russelli (Plaintail Turkeyfish), western Indo-Pacific (Wilcox et al. 2018).

Pterois miles
Pterois miles (Devil-Firefish) can be distinguished from P. volitans only by meristic counts and molecular analyses (Schultz 1986; . It is native to the western Indo-Pacific, and has also been introduced to the Western Atlantic (Schultz 1986; Hamner et al. 1997). Where the species have been distinguished, P. miles has been much rarer than P. volitans (Hamner et al. 2004; Guzmán-Méndez et al. 2017).

Pterois russelli
Pterois russelli (Plaintail Turkeyfish), western Indo-Pacific, is closely related to P. volitans (Red Lionfish), eastern Indo-Pacific, and P. lunulata (Luna Lionfish), a Northwest Pacific native (Wilcox et al. 2018).



Red Lionfish (Pterois volitans) have separate sexes, and spawn in pairs, after a courtship ceremony. Male lionfish mature at about 100 mm, and females at about 180 mm. Lionfish are synchronous, ineterminant spawners. The ovaries contain eggs in all stages of development, and spawning can take place year-round. Mature eggs have a mean diameter of 804 um, Eggs are released in a mass, with an estimated 24,630 eggs, surrounded by a ball of mucus. Egg masses are released, two at a time, near the surface (Morris et al. 2009; Morris and Whitfield 2009; Morris et al. 2011; Gardner et al. 2015). In North Carolina, Lionfish spawn about every four days, resulting in an annual fecundity of about two million eggs per year (Morris and Whitfield 2009). The larvae remain in the plankton for 20-35 days, as estimated from daily otolith rings (Ahrenholtz and Morris 2010). The planktonic larvae hatch with a yolk-sac, which is resorbed, and then feed on plankton. The offshore spawning locations, larval period, and pelagic mode of development permit long-distance dispersal by currents (Morris and Whitfield 2009; Morris et al. 2009; Vasquez-Yeomans et al. 2011; Kitchens et al. 2017). Settlement probably takes place predominantly but not exclusively in shallow habitats, including mangroves, seagrasses, estuaries, and around man-made structures, where juvenile lionfish are more common. Larger fish tend to predominate in deep-reef habitats (Biggs and Olden 2011; Claydon et al. 2012; Jud et al. 2011; Cure et al. 2014).

The Red Lionfish is generally regarded as a strictly marine, and tropical fish, but it is highly mobile and versatile, capable of using a wide range of habitats. In experiments where temperature was decreased gradually, the mean lethal temperature was 10 C, while feeding ceased at 16 C. In the field, populations off NC, were limited by a 12 C isotherm (Kimball et al. 2004), permitting the fish to winter in Gulf Stream-influenced waters (Kimball et al. 2004). The mean temperature for Lionfish in Onslow Bay, North Carolina was 15.3 C, at a depth of 38-46 M (Whitifield et al. 2014). Upper lethal temperature, determined as a critical thermal maximum (CTM), was 34-39 C (Aiken et al. 2014). Juvenile and adult lionfish were found through much of the Loxahatchee estuary, Florida (Jud et al. 2011). Lionfish survived 28 days at 7 PSU with no mortality or changes in behavior, feeding and growth. Fish in the Loxahatchee estuary occasionally occurred at salinities as low as 1 PSU, but did not survive prolonged exposure to these conditions (Jud et al. 2011; Schofield et al. 2015). Lionfish utilize a range of habitats, including coral reefs, mangroves, seagrass beds, and man-made structures, such as pilings (Barbour et al. 2010; Biggs and Olden 2011; Claydon et al. 2012; Jud et al. 2011; Pimiento et al. 2013). Lionfish have been widely reported in shallow water, but also from the mesophotc zones at the base of reefs, and from deeper slope waters at 200-300 m depth (Gress et al. 2017). The visual system of lionfishes are similar to those of Western Atlantic estuarine piscivores, but they are more sensitive to hypoxia, which could limit their penetration into estuaries (Hasenei et al. 2020).

Juvenile and adult Lionfishes are carnivorous. In the Loxahatchee River estuary, where juvenile fish predominated, the prey were about half-and-half fishes and crustaceans (crabs and shrimps). By weight, penaeid shrimps, blennies, and Gerreidiae (mojarras, a small perch-like fish) predominated (Jud and Layman 2011). On reefs in the Bahamas, Côté and Maljkovic (2010) observed Lionfish consuming many species of reef fishes. Lionfishes hunt throughout the diel cycle, but feeding rates are highest near dawn and sunset, and on overcast days (Côté and Maljkovic 2010; Green et al. 2011). In experiments, feeding rates were higher under white or blue light than red light, and lowest in darkness. Attack rates were much higher in environments of low habitat complexity (South et al. 2017).

Lionfishes' long-venomous spines limit predation, but they are eaten by native Nassau Groupers (Epinephelus striatus) (Maljkovic and Van Leeuwen 2008; Mumby et al. 2011). Lionfish can be eaten by humans, when the spines are removed, and are highly regarded as food in Asia. Fisheries are being encouraged in the Caribbean, as a possible means of population control (Morris et al. 2012). Introduced populations of lionfish have a much lower incidence of parasites than populations in the naitve range (Tuttle et al. 2017). Lionfish are not social or schooling, but do aggregate in structurally complex habitats. This might aid the development of artificial structures for the attraction and acpture of Lionfish (Hunt et al. 2019).


Crustaceans (shrimps), Fishes, Crabs


Humans; fishes

Trophic Status:




General HabitatCoral reefNone
General HabitatUnstructured BottomNone
General HabitatRockyNone
General HabitatMarinas & DocksNone
General HabitatCoarse Woody DebrisNone
Tidal RangeSubtidalNone
Vertical HabitatEpibenthicNone
Vertical HabitatNektonicNone

Life History

Tolerances and Life History Parameters

Minimum Temperature (ºC)9.5Minimum CT min (Barker et al. 2017)
Maximum Temperature (ºC)39.5Aikins et al. 2014 Critical Thermal Maximum, Aikens et al. 2014; Barker et al. 2017
Minimum Salinity (‰)7Experimental (Jud et al. 2014; Schofield et al. 2015). Long-term survival and growth occurred at 10-34 PSU (Schofield et al. 2015), but lionfish tolerated short exposures (>7 days) at 4-5 PSU (Jud et al. 2014; Schofield et al. 2015).
Maximum Salinity (‰)36Typical Gulf of Mexico salinity
Minimum Duration20Approximate time from hatching to settlement, based on daily otolith rings, Bahamas (Ahrenholz and Morris 2010)
Maximum Duration35Approximate time from hatching to settlement, ased on daily otolith rings, Bahamas (Ahrenholz and Morris 2010)
Minimum Length (mm)100Minimum for males, 170 mm for females (Morris and Whitfield 2019); Morris et al. 2011
Maximum Length (mm)467Bermuda (Eddy et al. 2019); 457 mm Ehemann (2017 , One specimen, Venezuela)
Broad Temperature RangeNoneSubtropical-Tropical
Broad Salinity RangeNoneMesohaline-Euhaline

General Impacts

Regional Impacts

CAR-VNoneEcological ImpactPredation
In transplantation experiments, patch reefs with a transplanted lionfish had reduced recruitment of juvenile native fishes. Juvenile native fishes were found in the lionfishes' gut contents (Albins and Hixon 2008; Albins et al. 2017). Mortality rates in a small fish, Gramma loreto (Fairy Basslet) greatly increased after the lionfish invasion, compared with a pre-invasion experiment (Ingeman and Webster 2015). In later experiments, in which prey and lionfish densities were maipulated, some low-density basslet populations were extirpated by lionfish predation (Ingeman et al. 2016). Isotopic values (15N, 13C) values varied, but shopwed an increasing trophic niche and diversity for large lionfish (Malpici-Cruz et al. 2019). Juveniles of the native Striped Parrotfish (Scarus iseri) have an unlearned response to Nassau Grouper (Epinephelus striatus but have to learn avoidance of Pterois spp. (Berchtold and Cote 2020).
CAR-VNoneEcological ImpactHabitat Change
Predation by lionfish has decreased local populations of herbivorous fishes, resulting in increased macroalgal populations at deeper depths, resulting in declines of corals and sponges (Lesser and Slattery 2011).
CAR-VNoneEcological ImpactTrophic Cascade
Predation by lionfish has decreased local populations of herbivorous fishes, resulting in increased macroalgal populations at deeper depths, resulting in declines of corals and sponges (Lesser and Slattery 2011). Predation by Lionfish resulted in reduced grazing by herbivorous fishes on algae, both through direct predation, but also by inducing behavioral changes, with reduced abundances of small fishes in the presence of lionfish (Kindinger and Albins 2016). Differential predation affected competitive relations between planktivorous fairy and blackcap basslets (Gramma loreto and Gramma melacara) (Kindinger 2018). Predation by lionfish affected the abundance of one abundant cleaner fish (Thalassoma bifasciatum, Bluehead Wrass), but did not affect another Elacatinus genie (Cleaner Goby). Cleaner fishes affect the health and social behavior of coral reef fish communities by removing parasites (Tuttle 2017),
CAR-IVNoneEconomic ImpactHealth
Ciguatera toxin was found in Lionfish in St. Maarten in 2011. and people were advised not to eat the fish (Associated Press 2011). Howver, test results on uncooked lionfish can be misleading, because they contain another group of toxins (Scorpaenitoxins), which give positive results, but are destroyed by cooking (Hixon et al. 2015). In Martinique, 117 patients in 2011-2014, stung by lionfish spines, were examined. All had local swelling. Other common symptoms were more extensive swelling, gastointestinal disorders, abdominal cramps, fainting, tachycardia, and hyptertension. Immersion of the stung area in warm water reduced pain duration and the chance of infection (Reisiere et al. 2015).
CAR-VIICape Hatteras to Mid-East FloridaEcological ImpactPredation
The population increase in Pterois spp. (mostly P. volitans) from 1990 to 2014 has been associated with a 45% decline of a common native fish, Tomtate (Haemulon aurolineatum) (Ballew et al. 2016).
CAR-IVNoneEcological ImpactPredation
Lionfish were found to be feeding on a newly described goby (Palatogobius incendius) living in deep-water mesophotic reef areas (Tornabene and Baldwin 2017).
CAR-IIINoneEcological ImpactPredation
Lionfish were found to be feeding on a newly described goby (Palatogobius incendius) living in deep-water mesophotic reef areas (Tornabene and Baldwin 2017)
S200Biscayne BayEcological ImpactCompetition
A native predator, Cephalopholis cruentata consumed less prey in areas of high lionfish density, but condition of the native fish was not affected (Curtis et al. 2017).
CAR-INorthern Yucatan, Gulf of Mexico, Florida Straits, to Middle Eastern FloridaEcological ImpactCompetition
A native predator, Cephalopholis cruentata consumed less prey in areas of high lionfish density, but condition of the native fish was not affected (Curtis et al. 2017).
CAR-INorthern Yucatan, Gulf of Mexico, Florida Straits, to Middle Eastern FloridaEcological ImpactPredation
Lionfishes in natural habitats and artificial reefs consumed a wide range of fish and invertebrate prey, with increasing piscivory in larger fish. Thirty-three species of prey were identified (Dahl and Patterson 304; Dahl et al. 2017). Modeling indicates that populations of several important grouper and snapper species (particularly Epinephelus morio Red Grouper) could be affected by high predicted abundances of lionfish off the Florida peninsula and Texas Gulf Coast (Johnston et al. 2017). Caging experiments in the Loxahatchee estuary of the Indian River Lagoon found that Lionfish caused a 90% reduction in Grass Shrimp (Palaemon) abundance, and a general reduction of benthic invertebrate abundance and diversity (Layman et al. 2014). Experimental studies and modeling indicate that P. volitians had a higher predation impact than two native predators (Epinephalus morio, Red Grouper; Cephalopholis cruentata, Graysby Grouper), because of the combination of high predator efficiency and high abundance (DeRoy et al. 2020).
CAR-INorthern Yucatan, Gulf of Mexico, Florida Straits, to Middle Eastern FloridaEconomic ImpactFisheries
Modeling indicates that populations of several commercially important grouper and snapper species (particularly Epinephelus morio Red Grouper) could be affected by high predicted abundances of lionfish off the Florida peninsula and Texas Gulf Coast. Control methods should be focused on these areas (Johnston et al. 2017).
S190Indian RiverEcological ImpactPredation
Caging experiments in the Loxahatchee estuary of the Indian River Lagoon found that Lionfish caused a 90% reduction in Grass Shrimp (Palaemon) abundance, and a general reduction of benthic invertebrate abundance and diversity (Layman et al. 2014).
NA-ET4BermudaEcological ImpactPredation
Lionfish in Bermuda preyed on a wide range of fishes and crustaceans (from 46 families), including ecologically important and economically improtant species (Eddy et al. 2017).
FLFloridaEcological ImpactCompetition
A native predator, Cephalopholis cruentata consumed less prey in areas of high lionfish density, but condition of the native fish was not affected (Curtis et al. 2017).
FLFloridaEcological ImpactPredation
Caging experiments in the Loxahatchee estuary of the Indian River Lagoon found that Lionfish caused a 90% reduction in Grass Shrimp (Palaemon) abundance, and a general reduction of benthic invertebrate abundance and diversity (Layman et al. 2014).

Regional Distribution Map

Bioregion Region Name Year Invasion Status Population Status
EAS-VI None 0 Native Estab
EAS-VII None 0 Native Estab
EAS-I None 0 Native Estab
EAS-VIII None 0 Native Estab
AUS-XVIII None 0 Native Estab
SP-VII None 0 Native Estab
SP-XII None 0 Native Estab
NWP-2 None 0 Native Estab
NWP-4a None 0 Native Estab
EAS-III None 0 Native Estab
AUS-I None 0 Native Estab
AUS-XIII None 0 Native Estab
SP-XVI None 0 Native Estab
EAS-II None 0 Native Estab
AG-3 None 0 Native Estab
SP-XX None 0 Native Estab
SP-XIII None 0 Native Estab
SP-I None 0 Native Estab
SP-II None 0 Native Estab
EAS-IV None 0 Native Estab
SP-IX None 0 Native Estab
SP-III None 0 Native Estab
NWP-3a None 0 Native Estab
SP-V None 0 Native Estab
CAR-I Northern Yucatan, Gulf of Mexico, Florida Straits, to Middle Eastern Florida 1985 Def Estab
CAR-VII Cape Hatteras to Mid-East Florida 2000 Def Estab
NA-ET4 Bermuda 2000 Def Estab
NA-ET3 Cape Cod to Cape Hatteras 2001 Def Unk
M020 Narragansett Bay 2006 Def Unk
G074 _CDA_G074 (Crystal-Pithlachascotee) 2006 Def Estab
CAR-II None 2007 Def Estab
CAR-V None 2004 Def Estab
CAR-IV None 2008 Def Estab
CAR-III None 2008 Def Estab
M050 Great South Bay 2001 Def Failed
M065 _CDA_M065 (Middle Delaware-Mongaup-Broadhead) 2003 Def Failed
S180 St. Johns River 0 Def Estab
S190 Indian River 2002 Def Estab
S183 _CDA_S183 (Daytona-St. Augustine) 2002 Def Estab
S196 _CDA_S196 (Cape Canaveral) 1995 Def Estab
S200 Biscayne Bay 1992 Def Estab
S175 _CDA_S175 (Nassau) 0 Def Estab
S206 _CDA_S206 (Vero Beach) 2009 Def Estab
EAS-V None 0 Native Estab
AUS-XII None 0 Native Estab
SP-XIV None 0 Native Estab
SP-XI None 0 Native Estab
AUS-II None 0 Native Estab
AUS-III None 0 Native Estab
SP-XIX None 0 Native Estab
G010 Florida Bay 2010 Def Estab
G070 Tampa Bay 2010 Def Estab
G130 Pensacola Bay 2010 Def Estab
G200 Barataria Bay 2010 Def Estab
G150 Mobile Bay 2010 Def Estab
G100 Apalachicola Bay 2010 Def Estab
G120 Choctawhatchee Bay 2010 Def Estab
G330 Lower Laguna Madre 2011 Def Estab
M130 Chesapeake Bay 2013 Def Unk
G108 _CDA_G108 (St. Andrew-St. Joseph Bays) 0 Def Estab
G110 St. Andrew Bay 2011 Def Estab
G140 Perdido Bay 2010 Def Estab
G160 East Mississippi Sound 2013 Def Unk
G260 Galveston Bay 2013 Def Estab
SA-II None 2014 Def Estab
PAN_CAR Panama Caribbean Coast 2009 Def Estab
S013 _CDA_S013 (Pamlico Sound) 2010 Def Estab
SA-IV None 2020 Def Estab
SA-III None 2020 Def Estab

Occurrence Map

OCC_ID Author Year Date Locality Status Latitude Longitude


Curtis, Lyanne J. F; Pearce, Christopher M.; Hodes, Vanessa; Nelson, Jocelyn C.; Wasser, Calley; Savery, Julia;; Therriault, Thomas W. (2021) Mitigating non-indigenous species movements: effects of pressure-washing intensity and duration on the removal of biofouling and mobile invertebrates from cultured Pacific oysters (Crassostrea gigas) (Thunberg, 1793), Management of Biological Invasions 12: Inpres

Acuña, Fabián H.; Garese, Agustín; Excoffon, Adriana C.; Cortés, Jorge (2013) New records of sea anemones (Cnidaria: Anthozoa) from Costa Rica, Revista de Biología Marina y Oceanografía 48(1): 177-184
DOI 10.4067/S0718-19572013000100015

Aguilar-Perera, Alfonso; Tuz-Sulub, Armin (2010) Non-native, invasive Red lionfish (Pterois volitans [Linnaeus, 1758]: Scorpaenidae), is first recorded in the southern Gulf of Mexico, off the northern Yucatan Peninsula, Mexico, Aquatic Invasions 5(2): <missing location>

Ahrenholz, Dean W.; Morris, James A. Jr. (2010) Larval duration of the lionfish, Pterois volitans along the Bahamian Archipelago, Environmental Biology of Fishes 88: 305-309

Aikens, Christer and 6 authors 2014 The critical thermal maximum of Lionfish (<i>Pterois volitans</i>). Island School; Cape Eleuthera Institute

Airey , Montana E. ; Fogg, Alexander Q. · Drew Joshua A. D (2023) Invasive lionfish dispersal between shallow‑ and deep‑water habitats within coastal Floridian waters, Biological Invasions 25: 3983–3991

Albins, Mark A.; Hixon, Mark A. (2008) Invasive Indo-Pacific lionfish Pterois volitans reduce recruitment of Atlantic coral-reef fishes., Marine Ecology Progress Series 367: 233-238

Albins, Mark A.; Hixon, Mark A. (2013) Worst case scenario: potential long-term effects of invasive predatory lionfish (Pterois volitans) on Atlantic and Caribbean coral-reef communities, Environmental Biology of Fishes 96: 1151-1157

Albins, Mark A.; Lyons, Patrick J. (2012) Invasive red lionfish Pterois volitans blow directed jets of water at prey fish, Marine Ecology Progress Series 448: 1-5

Alphin, Troy D.; Posey, M. H. ; Smith, M E. (1997) Comparison of infauna associated with the macroalga Caulerpa prolifera found in southeastern North Carolina, Journal of the Elisha Mitchell Scientific Society 113(1): 16-21

Anonymous 2021 Ascidians of the Eastern Cape. <missing description>

Anton, Andrea; Cure, Katherine; Layma, Craig A.; Puntila, Riikka; Simpson, Michael S.; Bruno, John F. (2016) Prey naiveté to invasive lionfish Pterois volitans on Caribbean coral reefs, Marine Ecology Progress Series 544: 257-269

Arias-Gonzalez, Jesus Ernesto; Gonzalez-Gandara, Carlos; Cabrera, Jose´ Luis; Christensen, Villy (2011) Predicted impact of the invasive lionfish Pterois volitans on the foodweb of a Caribbean coral reef, Environmental Research 111: 917-925

Associated Press 11/24/2011 St Maarten nixes plan to promote lionfish as food after tests show some meat tainted. <missing description>

Banta, William C.;Redden 1990 (1990) A checklist of the bryozoa of the Galapagos Islands, Proceedings of the Biological Society of Washington 103(4): 789-802

Barbour, Andrew B.; Allen, Michael S.; Frazer, Thomas K.; Sherman, Krista D. (2011) Evaluating the potential efficacy of invasive lionfish (Pterois volitans) removals, PLOS ONE 6(5): e19666 (published on

Barbour, Andrew B.; Montgomery, Meredith L.; Adamson, Alecia A.; Díaz-Ferguson, Edgardo; Silliman, Brian R. (2010) Mangrove use by the invasive lionfish Pterois volitans, Marine Ecology Progress Series 401: 291-294

Bejarano, Sonia; Lohr, Kathryn; Hamilton, Samantha; Manfrino, Carrie (2015) Relationships of invasive lionfish with topographic complexity, groupers, and native prey fishes in Little Cayman, Marine Biology 162: 253-266

Benitt, Colin; Young, Craig S.; Sylvers, Laine H.; Gobler, Christopher J. (2022) Inhibition of harmful algal blooms caused by Aureococcus anophagefferens (Pelagophyceae) using native (Gracilaria tikvahiae) and invasive (Dasysiphonia japonica) red seaweeds from North America, Journal of Applied Phycology 34: 965–983

Benkwitt, Cassandra E. (2013) Density-dependent growth in invasive lionfish (Pterois volitans), PLOS ONE 8(6): e66995

Benkwitt, Cassandra E. (2015) Non-linear effects of invasive lionfish density on native coral-reef fish communities, Biological Invasions 17: 1383-1395

Bernal, Nicholas A.; DeAngelis, Donald L; Schofield, Pamela J.; Sealey, Kathleen Sullivan (2015) Predicting spatial and temporal distribution of Indo-Pacific lionfish (Pterois volitans) in Biscayne Bay through habitat suitability modeling, Biological Invasions 17: 1603-1614

Betancur-R., Ricardo and 5 authors (2011) Reconstructing the lionfish invasion: insights into Greater Caribbean biogeography, Journal of Biogeography 38: 1281-1293

Biggs, Christopher R.; Olden, Julian D. (2011) Multi-scale habitat occupancy of invasive lionfish (Pterois volitans) in coral reef environments of Roatan, Honduras, Aquatic Invasions 6: corrected proof

Black, Andrew N.; Weimann, Sonia R.; Imhoff, Vance E.; Richter, Martin L. ; Itzkowitz, Murray (2014) A differential prey response to invasive lionfish, Pterois volitans: Prey naiveté and risk-sensitive courtship, Journal of Experimental Marine Biology and Ecology 460: 1-7

Briggs, Philip T.; Waldman, John R. (2002) Annotated list of fishes reported from the marine waters of New York, Northeastern Naturalist 9(1): 47-80

Brossi-Garcia, Ana Luiza, Moreira, Renata Guimarães (1992) Estudos biométricos e morfológicos dos primeiros estágios juvenis de Petrolisthes armatus (Gibbes, 1850) (Decapoda, Porcellanidae) em laboratório, Revista Brasileira de Biologia 56(2): 231-243

Brown-Peterson, Nancy J.; Hendon, J. Read (2013) Notes on the biology of invasive lionfish (Pterois sp. In the northcentral Gulf of Mexico, Gulf and Caribbean Research 25: 117-120

Bullard, S. A.; Barse, A. M.; Curran, S. S.; Morris, J. A., Jr. (2011) First record of a digenean from invasive lionfish, Pterois cf. volitans, (Scorpaeniformes: Scorpaenidae) in the northwestern Atlantic Ocean, Journal of Parasitology 97(5): 833-837

Butterfield, John S. S. and 8 authors (2015) Wide-ranging phylogeographic structure of invasive red lionfish in the Western Atlantic and Greater Caribbean, Marine Biology 162: 773-781

Calado, Ricardo; Chapman, Peter M. (2006) Aquarium species: Deadly invaders., Marine Pollution Bulletin 52: 599-601

Calazans, Savio H.; Walters, Linda J.;; Fernandes, Flavio C. , Ferreira, Carlos E. L. ; Hoffman, Eric; A. (2017) Genetic structure provides insights into the geographic origins and temporal change in the invasive charru mussel (Sururu) in the southeastern United States, PLOS ONE 12(7): e0180619

Calder, Dale R.; Carlton, James T.; Keith, Inti; Ashton, Gail V. ;Larson, Kristen; Ruiz, Gregory M.; Herrera, Esteban; Golfin, Geiner (2017) Biofouling hydroids (Cnidaria: Hydrozoa) from a tropical Eastern Pacific island, with remarks on their biogeography, Journal of Natural History 56(9-12): 565-606

Campbell, Matthew D. and 10 authors (2021) Rapid spatial expansion and population increase of invasivelionfish (Pterois spp.) observed on natural habitats in the northern Gulf of Mexico, Biological Invasions Published online: <missing location>

Campbell, Matthew D. and 9 authors (2022) Rapid spatial expansion and population increase of invasive lionfish (Pterois spp.) observed on natural habitats in the northern Gulf of Mexico, Biological Invasions 24: 93-105

Cerino, David; Overton, Anthony S.; Rice, James A.; Morris, James A. Jr. (2013) Bioenergetics and trophic impacts of the invasive Indo-Pacific lionfish, Transactions of the American Fisheries Society 142: 1522-1534

Cerwenka, Alexander F. ; Brandner, Joerg; Dashinov, Dimitriy; Geist, Juergen (2023) Small but Mighty: The Round Goby (Neogobius melanostomus) as a Model Species of Biological Invasions, Diversity 15(528): Published online d15040528

Chaves, L. C. T.; Hall, J.; Feitosa, J. L. L.; Côté, I. M. (2016) Photo-identification as a simple tool for studying invasive lionfish Pterois volitans populations, Journal of Fish Biology 88: 800-804

Chong, Samuel S. C. ; Khoo, H. W.; Ng, Peter K. L. (1987) Presence of the Japanese freshwater Prawn Macrobrachium nipponense (De Haan, 1849) (Decapoda: Caridea: Palaemonidae) in Singapore., Zoollogische Mededelingen 61(11): 314-317

Claydon, John Alexander Brightman; Calosso, Marta Caterina; Traiger, Sarah Beth (2012) Progression of invasive lionfish in seagrass, mangrove and reef habitats, Marine Ecology Progress Series 448: 119-129

Cote, Isabelle M. and 6 authors (2014) What doesn’t kill you makes you wary? Effect of repeated culling on the behaviour of an invasive predator, PLOS ONE 9(4): e94248

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WPEC TV 12 2011 Invasive, destructive lionfish found in Loxahatchee River.