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Atractosteus

Atractosteus is a genus of primitive ray-finned fishes in the family Lepisosteidae (gars), consisting of three extant species native to the tropical and subtropical freshwater and brackish waters of North and Central America.^[1] These species are characterized by their elongate, torpedo-shaped bodies covered in heavy, rhomboidal ganoid scales that interlock like armor, long conical snouts resembling those of alligators, and jaws lined with sharp, needle-like teeth arranged in a double row on the upper jaw.^[1]^[2] Known as living fossils, Atractosteus species retain ancient morphological features that trace back over 100 million years to the Cretaceous period.^[3] The genus includes the alligator gar (A. spatula), the largest freshwater fish in North America, which can exceed 3 meters in length and 150 kilograms in weight; the Cuban gar (A. tristoechus), endemic to Cuba; and the tropical gar (A. tropicus), distributed from Mexico to Costa Rica.^[4]^[5] All three species inhabit rivers, lakes, swamps, and coastal bays, often ambushing prey such as fish, amphibians, birds, and small mammals from cover, and they are tolerant of low-oxygen environments thanks to a specialized swim bladder that functions as a lung.^[1]^[6] Atractosteus was formally recognized as a distinct genus by ichthyologist E. O. Wiley in 1976, separating it from the related genus Lepisosteus based on differences in dentition, scale patterns, and phylogenetic relationships derived from fossil and recent specimens.^[7] While the alligator gar has faced population declines due to habitat loss, overfishing, and barriers to migration, leading to protections in parts of the United States, the Cuban gar is critically endangered, the genus as a whole highlights the ecological importance of these apex predators in maintaining aquatic food webs.^[3]^[8] Fossil records indicate that ancestors of Atractosteus once inhabited marine environments, underscoring their evolutionary adaptability.^[1]

Taxonomy and Systematics

Classification History

The genus Atractosteus was first proposed by Constantine Samuel Rafinesque in 1820 as a subgenus within Lepisosteus in his seminal work Ichthyologia Ohiensis, distinguishing certain gar species based on preliminary morphological observations of North American freshwater fishes.^[9] This initial classification reflected the limited systematic knowledge of the time, where gars were broadly grouped without detailed comparative anatomy. The name Atractosteus derives from the Greek words atraktos (meaning spindle or arrow) and osteon (bone), alluding to the genus's characteristic elongated, spindle-shaped bony skeleton covered in ganoid scales.^[10] Over the subsequent century and a half, Atractosteus was largely treated as a junior synonym of Lepisosteus, with species like the alligator gar (L. spatula) remaining classified under the latter genus in most ichthyological catalogs. This lumping stemmed from traditional morphological assessments that overlooked subtle differences in cranial and postcranial osteology. Historical classifications also embedded gars, including Atractosteus, within the broader Holostei clade alongside bowfins (Amia), viewing them as a paraphyletic assemblage of "living fossils" without resolving their monophyly or interrelationships.^[11] A pivotal revision occurred in 1976 when E. O. Wiley elevated Atractosteus to full generic status in his dissertation The Phylogeny and Biogeography of Fossil and Recent Gars (Actinopterygii: Lepisosteidae), based on a cladistic analysis of osteological characters such as differences in the supraorbital canal, parietal bones, and gular plates. Wiley transferred three extant species—Lepisosteus spatula (alligator gar), L. tristoechus (Cuban gar), and L. tropicus (tropical gar)—to Atractosteus, distinguishing it from Lepisosteus through shared derived traits like a more robust snout and modified infracthnals. This work marked the adoption of cladistic methods in gar systematics, resolving prior misclassifications and establishing Atractosteus as a valid, monophyletic genus within Lepisosteidae, a classification upheld in subsequent phylogenetic studies.

Phylogenetic Position

_Atractosteus is classified within the order Lepisosteiformes and the family Lepisosteidae, representing one of the two extant genera in this family alongside Lepisosteus []. The genus is characterized as the sister group to Lepisosteus, a relationship supported by shared semionotiform traits, including ganoid scales composed of layers of bone, ganoine, and cosmine, as well as a vascularized swim bladder that functions in both buoyancy and respiration []. These morphological synapomorphies place Atractosteus firmly within the broader clade of ginglymodians, highlighting the conservative evolutionary history of lepisosteids as "living fossils" with ancient body plans []. Cladistic analyses based on extensive skeletal anatomy have positioned Atractosteus as a derived lineage within Ginglymodi, the larger group encompassing semionotiform fishes []. In particular, comprehensive phylogenetic studies incorporating both extant and fossil taxa indicate that basal divergences leading to modern lepisosteids occurred during the Late Jurassic, with Atractosteus evolving as a monophyletic group distinguished by specialized features such as robust cranial bones and predatory adaptations []. This placement underscores the deep divergence between Atractosteus and Lepisosteus, estimated to have occurred in the Early Cretaceous based on integrated morphological and temporal data []. Molecular phylogenies, derived from mitochondrial and nuclear DNA sequences, corroborate the monophyly of Atractosteus, with strong bootstrap support for its distinction from Lepisosteus []. These analyses highlight unique dental and cranial synapomorphies, such as enlarged premaxillary fangs and a shortened parasphenoid, as key molecularly corroborated traits defining the genus []. The congruence between molecular and morphological evidence reinforces Atractosteus's phylogenetic stability, with no significant conflicts in tree topologies across studies [].

Species Overview

The genus Atractosteus includes three extant species of gars in the family Lepisosteidae. A. spatula, known as the alligator gar, is native to the Mississippi River basin from southwestern Ohio and southern Illinois to the Gulf of Mexico, and the Gulf Coastal Plain from Florida to Texas. A. tristoechus, the Cuban gar, is endemic to western Cuba and Isla de la Juventud. A. tropicus, the tropical gar, inhabits rivers and lakes in the Caribbean and Pacific drainages of southern Mexico and Central America, from Guatemala to Costa Rica.^[12] These species are distinguished by subtle morphological differences adapted to their environments. A. spatula is the largest, capable of reaching over 3 m in length, with a characteristically broad, short snout and a double row of large teeth on the upper jaw, giving it an alligator-like appearance. A. tristoechus grows to a maximum of about 2 m and features a more slender profile, with juveniles displaying ornate spotting for camouflage. A. tropicus is the smallest extant species, typically under 1.3 m, with an elongated body resembling a floating log and a narrower snout compared to A. spatula.^[13]^[14] The genus is phylogenetically distinct from the related Lepisosteus primarily through derived features in cranial morphology and dentition.^[15]

Physical Description

General Morphology

Atractosteus species are characterized by an elongated, torpedo-shaped body that tapers toward the rear, providing hydrodynamic efficiency for ambushing prey in aquatic environments. This body plan is armored with interlocking ganoid scales arranged in rhomboid patterns, forming a rigid protective covering that enhances durability against predators and environmental stresses.^[2]^[6] The scales are heavy and diamond-shaped, consisting of a basal bony layer overlaid with a thin, enamel-like ganoine coating that imparts high hardness and resistance to abrasion.^[16] The head features a prominent, elongated beak-like snout that accounts for more than half of the total head length, housing rows of sharp, conical teeth adapted for grasping.^[17] The tail is heterocercal, with the vertebral column extending into the upper lobe, though the overall fin appears rounded due to an abbreviated structure that balances propulsion and maneuverability. Maximum body lengths reach up to 3 m in A. spatula, with other species in the genus typically attaining 1–2 m, such as A. tropicus at around 1.25 m.^[18]^[19] The dorsal and anal fins are positioned far posteriorly on the body, nearly opposite each other near the tail base, which aids in maintaining stability and control during bursts of speed.^[6] This configuration, combined with low-placed pectoral and pelvic fins, supports the species' predatory lifestyle in slow-moving waters. Maximum recorded weights exceed 130 kg for A. spatula, reflecting their substantial biomass in mature individuals.^[20] Lifespans extend up to 50–70 years, as validated through otolith annuli analysis that reveals incremental growth rings corresponding to annual cycles.^[21]

Diagnostic Features

Atractosteus species are distinguished from other gar genera by several distinctive cranial and dental features that facilitate their predatory lifestyle. A primary diagnostic trait is the double row of large, conical teeth lining the underside of the upper jaw, contrasting with the single row observed in the closely related genus Lepisosteus. This arrangement enhances prey retention during strikes, with the inner row positioned palatally to interlock with lower jaw teeth.^[2] The adult head is broad and spade-shaped, characterized by a short, robust snout formed by fused premaxillae that create a solid, reinforced beak-like structure. This morphology provides greater structural integrity compared to the more elongate, needle-like snout of Lepisosteus species, supporting the capture of larger or more elusive prey. The snout surface features numerous sensory pores associated with electroreceptive ampullary organs, enabling detection of bioelectric fields from prey in turbid waters.^[18]^[22] Internally, Atractosteus possesses a highly vascularized swim bladder that functions as an accessory lung, allowing bimodal respiration through air gulping at the water surface. This adaptation is supported by a pneumatic duct connecting the esophagus to the bladder, with richly vascularized walls facilitating gas exchange in hypoxic environments.^[23] Osteologically, the genus exhibits a reduced number of branchiostegal rays (typically 3), fewer than in more basal ginglymodian ancestors, contributing to a streamlined gular region beneath the compact head.^[24]

Distribution and Habitat

Geographic Range

The genus Atractosteus exhibits a distribution spanning the Nearctic and Neotropical realms, primarily in North and Central America, with one species endemic to the Caribbean.^[18]^[13]^[25] Atractosteus spatula, the alligator gar, is native to the Mississippi River basin, extending from southwestern Ohio and southern Illinois southward through the central United States to the Gulf of Mexico, as well as the Gulf Coastal Plain from the Econfina River in Florida westward to Veracruz, Mexico.^[18]^[7]^[6] This species occupies freshwater rivers, bayous, and brackish coastal estuaries within its range.^[26] Historical records indicate a broader extent in the northern Mississippi basin, but populations have been extirpated from many upstream areas due to habitat alterations.^[20] Introductions of A. spatula have occurred in other U.S. states, including isolated aquarium releases in California and South Carolina, though no self-sustaining populations have established outside the native range.^[20]^[27] Atractosteus tristoechus, the Cuban gar, is restricted to western Cuba, including the mainland and Isla de la Juventud, where it inhabits swampy rivers, lakes, and coastal lagoons.^[13]^[28] This species' range is the most limited within the genus, confined to remnant wetlands in these regions.^[29] The species is classified as critically endangered by the IUCN, with populations declining due to habitat degradation and invasive species, further restricting its effective range.^[30] Atractosteus tropicus, the tropical gar, occurs across Central America from southern Mexico through Belize, Guatemala, Honduras, Nicaragua, and into Costa Rica, inhabiting drainages on both the Atlantic (Caribbean) and Pacific slopes.^[25]^[31]^[32] Its distribution includes large rivers and associated freshwater and brackish habitats in these tropical lowlands.^[33]

Environmental Preferences

Species of the genus Atractosteus primarily inhabit slow-moving, vegetated freshwater systems, including rivers, bayous, swamps, and lakes, where they exploit shallow, warm waters rich in aquatic vegetation. These environments provide essential cover and prey availability, with the genus showing a strong affinity for lowland riverine and floodplain habitats across their native ranges in North and Central America.^[34] Atractosteus species are euryhaline, demonstrating tolerance for brackish water conditions up to 24 ppt salinity, although optimal growth occurs in freshwater (0 ppt) to low salinity (up to 8 ppt), with reduced feeding rates and overall performance at higher salinities (8 ppt and above) in juveniles. They thrive in warm water temperatures typically ranging from 20°C to 32°C, with peak activity and recruitment associated with 20–30°C during spring and summer months. These fish are well-adapted to low dissolved oxygen levels in stagnant or hypoxic waters, relying on facultative air-breathing via a highly vascularized swim bladder to supplement gill respiration, which enables survival in oxygen-poor backwaters and vegetated shallows.^[35]^[36]^[37] Within these habitats, Atractosteus occupy microhabitats offering ambush opportunities, such as submerged vegetation, woody debris, and emergent plants, which provide concealment for predatory behavior. Juveniles preferentially utilize shallower, vegetated edge zones and flooded terrestrial areas, including backwaters and isolated tributaries, where floating debris and grasses offer refuge from predators during early development.^[34]^[38] The genus exhibits adaptations to seasonal flooding in riverine systems, migrating into inundated floodplains to access expanded vegetated areas for foraging and growth, a behavior that synchronizes with annual hydroperiods to enhance habitat connectivity and resource exploitation.^[39]

Biology and Ecology

Feeding Habits

Species of the genus Atractosteus, including the alligator gar (A. spatula), tropical gar (A. tropicus), and Cuban gar (A. tristoechus), exhibit primarily piscivorous diets, consuming a variety of fish such as gizzard shad (Dorosoma cepedianum), catfish, largemouth bass (Micropterus salmoides), and cichlids in proportion to their local abundance.^[40]^[41]^[42]^[13] In some populations, nongame fish dominate the diet, comprising over 85% of occurrences by number and weight, while sportfish represent less than 15%.^[40] Larger individuals opportunistically include crustaceans like blue crabs, waterfowl, small mammals, turtles, and even invasive amphibians such as cane toads (Bufo marinus), though these are infrequent compared to fish prey. The Cuban gar additionally preys on birds.^[6]^[43]^[44] These gars are ambush predators that lie motionless near the water surface or submerged, often resembling drifting logs, to detect approaching prey via their highly sensitive lateral line system and electrosensory ampullary organs.^[6]^[45] Upon detection, they lunge forward with explosive strikes, lashing their heads side-to-side to impale prey on interlocking, fang-like teeth that prevent escape.^[6] Prey size correlates positively with gar total length, allowing larger individuals to target bigger items.^[40] Ontogenetic shifts occur in feeding habits, with juveniles initially consuming invertebrates such as zooplankton (e.g., Artemia franciscana and cladocerans like Moina macrocopa) before transitioning to piscivory as they grow beyond 30 mm total length.^[46] Adults focus on larger fish, with seasonal variations influencing intake: feeding peaks in summer and fall when 83% of stomachs contain prey, dropping to 9% in winter-spring due to lower temperatures and prey availability.^[40] Selectivity analyses show positive bias toward certain species like buffalo (Ictiobus spp.) and neutral for shad, reflecting opportunistic foraging based on environmental abundance.^[40] As apex predators in freshwater and brackish ecosystems, Atractosteus species play a key role in regulating prey populations, potentially stabilizing food webs by controlling abundant forage fish and reducing overpopulation of invasive species, though their impact on sportfish is minimal.^[47]^[40] This trophic position underscores their importance in maintaining ecological balance in rivers, reservoirs, and estuaries.^[41]

Reproductive Biology

Atractosteus species exhibit sexual dimorphism, with females generally growing larger than males, which influences reproductive roles and fecundity. Sexual maturity is reached at varying ages across species and populations; for instance, in the tropical gar (A. tropicus), males mature within the first year and females within the second year, while in the alligator gar (A. spatula), males typically mature around age 6 and females around age 11. Maturity ages for the Cuban gar (A. tristoechus) are not well documented.^[48]^[5] Spawning occurs seasonally in spring or summer, often in communal groups, within flooded vegetated areas of floodplain tributaries that provide suitable substrates for egg adhesion.^[49] Reproduction involves external fertilization through broadcast spawning, where females release eggs that are adhesive and attach to submerged vegetation such as Carex species, while males simultaneously release milt; there is no parental care provided to the eggs or larvae.^[49] Females produce substantial clutches, with fecundity ranging from approximately 77,000 to 157,000 eggs per individual in A. spatula, varying based on body size and correlating positively with total length. Eggs are toxic to many predators, enhancing survival rates.^[6] Eggs typically hatch in 48–72 hours, with times varying inversely with water temperature (e.g., 2–3 days at 27.5–30°C for A. spatula; ~87–111 hours at 26–30°C for A. tristoechus).^[3]^[50]^[49] Larvae emerge with a prominent yolk sac, which is absorbed within about 3–5 days post-hatching, marking the transition to exogenous feeding; during this period, larvae remain attached to substrates via a larval attachment organ and exhibit rapid initial growth rates of 3.6–5.0 mm per day.^[51]^[49] Sex determination in Atractosteus is likely environmental, with evidence suggesting temperature-dependent mechanisms that can lead to skewed sex ratios in populations exposed to varying thermal regimes during early development.^[52]

Evolution and Fossil Record

Evolutionary Origins

The lepisosteoid fishes, the group encompassing the genus Atractosteus, trace their evolutionary origins to the Late Jurassic period, approximately 150–157 million years ago, as part of the broader radiation of Semionotiformes within the Ginglymodi clade of ray-finned fishes.^[53]^[54] Early lepisosteoids, the group encompassing modern gars including Atractosteus, likely emerged from ancestors similar to genera such as Semionotus, which exhibited semionotiform characteristics like ganoid scales and robust body plans adapted to Mesozoic aquatic environments.^[54] This radiation reflects a diversification of basal neopterygians, with fossils indicating an initial marine habitat before transitions to continental settings.^[55] Following their Late Jurassic origins, Atractosteus ancestors adapted to freshwater niches during the Early Cretaceous, coinciding with global environmental shifts that favored invasion of riverine and lacustrine systems.^[56] The development of air-breathing capabilities, facilitated by a lung-like swim bladder, evolved as a key adaptation to hypoxic conditions prevalent in these often oxygen-poor freshwater habitats, allowing gars to supplement gill respiration with atmospheric oxygen.^[57] This trait, homologous to the lungs of early sarcopterygians, underscores the retention of ancient vertebrate respiratory mechanisms in actinopterygians.^[58] Post-Cretaceous–Paleogene (K–Pg) extinction events further shaped this adaptation, with evidence of Atractosteus species rapidly recolonizing North American freshwater ecosystems within thousands of years of the asteroid impact, highlighting their resilience in recovering environments.^[59] A pivotal evolutionary event was the divergence of Atractosteus from its sister genus Lepisosteus around 105 million years ago in the Early Cretaceous, enabling subsequent radiations and colonization of Neotropical regions. While the stem lineage diverged around 105 million years ago, the crown clade of Atractosteus originated in the Cenozoic of eastern North America, serving as a center for extant diversity.^[60]^[61] This split facilitated the spread of Atractosteus species into Central American and Mexican freshwater systems, where modern taxa like A. tropicus persist. These ancient traits, including the vascularized swim bladder and predatory morphology, have been conserved across the lineage, linking Atractosteus phylogenetically to other extant gar species through shared lepisosteid synapomorphies.^[54]

Fossil Species

The fossil record of Atractosteus spans from the Santonian stage of the Late Cretaceous, approximately 86 million years ago, to the present, with the majority of well-documented specimens originating from Paleogene deposits in North America and scattered occurrences in Europe. This temporal range highlights the genus's resilience through major extinction events, including the Cretaceous-Paleogene boundary, though definitive fossils are relatively sparse compared to modern taxa. Major fossil sites include the Eocene Green River Formation in Wyoming, USA, and the Paleocene Hell Creek Formation in North Dakota, USA, alongside European localities such as the Eocene Messel Pit in Germany.^[62]^[63] One of the earliest and most significant fossil species is Atractosteus grandei, known from a nearly complete 1.5-meter-long skeleton discovered in the Hell Creek Formation of North Dakota, dated to the earliest Paleocene, just 1,500–2,500 years after the Cretaceous-Paleogene extinction event around 66 million years ago.^[63] This transitional form represents one of the oldest post-Cretaceous records of the genus, exhibiting morphological features intermediate between Late Cretaceous ancestors and later Eocene species, such as an elongated rostrum and robust gular plates indicative of adaptation to freshwater environments recovering from the asteroid impact.^[63] Its discovery underscores rapid recolonization of North American river systems by lepisosteids following the mass extinction.^[59] In the Early Eocene Green River Formation of Wyoming, Atractosteus simplex is represented by exceptionally well-preserved specimens, including articulated skulls that reveal early developments in dentition, such as double rows of sharp, conical teeth suited for grasping prey— a trait foreshadowing the predatory adaptations seen in modern Atractosteus species.^[62] These fossils, dating to approximately 50 million years ago, occur rarely in Fossil Lake deposits (less than 0.05% of the fish fauna) and provide insights into the genus's diversification in lacustrine habitats during a period of global warming.^[64] Also from the Green River Formation, Atractosteus atrox stands out as the largest known extinct species in the genus, with specimens reaching up to 1.8 meters in length, suggesting episodes of gigantism possibly linked to abundant food resources in Eocene lakes.^[62] Described from complete skeletons preserved in fine-grained limestones, this species features an elongated body and heavy ganoid scales similar to those of the extant alligator gar (A. spatula), but with proportionally larger jaws adapted for ambushing larger vertebrates.^[62] Its presence in the same formation as A. simplex indicates sympatric occurrence of multiple Atractosteus lineages during the Eocene.^[64] A potentially dubious species, Atractosteus africanus, is based on fragmentary remains from the Late Cretaceous (Santonian) Kem Kem Group in North Africa, including isolated scales and bones from what is now Niger, though erosion and incompleteness have led some researchers to question its assignment to Atractosteus and suggest it may represent a basal lepisosteid instead. These African fossils, dating to around 86 million years ago, extend the genus's early range beyond North America but lack sufficient diagnostic material for confident classification, highlighting gaps in the pre-Paleogene record.

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[PDF] PREDATION BY Atractosteus tropicus ON Bufo marinus AND ... - arXiv
Direct effects of predatory fish on amphibians mostly arise from consumption of adults and larvae (Hec- nar and M'Closkey 1997, Kiesecker and. Blaustein 1998, ...Missing: habits | Show results with:habits
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The primary projections of the lateral-line nerves of the Florida gar ...
Gars, like most other ray-finned fishes, possess lines of superficial and canal neuromasts that form highly ordered spatial arrays on the head and trunk.Missing: fish predation<|separator|>
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[PDF] Determination of optimal prey for rearing the Tropical Gar ...
Sep 1, 2018 · In the present study, we evaluated prey selectivity for the tropical gar Atractosteus tropicus in the larval stage (first 8 weeks) using the ...
[46]
[PDF] Advances in Conservation and Management of the Alligator Gar
2017). FOOD HABITS AND FEEDING ECOLOGY. Due to long-held beliefs that Alligator Gar selectively prey on desirable sport fish species, such as crappies. Pomoxis ...
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A day in the life of a gar lab - the Node
Jun 21, 2016 · The tropical gar (Atractosteus tropicus), on the other hand, reaches sexual maturity within the first (males) or second (females) year.Missing: reproductive | Show results with:reproductive
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[PDF] Spawning Ecology and Spawning Site Fidelity of Alligator Gar ...
May 3, 2024 · Alligator Gar (Atractosteus spatula) has declined relative to its historic range (Etnier and ... temperature range of 27.5-30.0°C. On 19 June,.Missing: tolerance | Show results with:tolerance
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Larval Development in Tropical Gar (Atractosteus tropicus) Is ... - MDPI
Hatching rate was significantly higher when Atractosteus tropicus eggs were incubated at 28 °C than at 24 °C (90.17 ± 4.67% vs. 85.17 ± 5.12%; ANOVA, p < 0.05).
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Sex-specific differences in transcriptome profiles of brain and ...
Apr 7, 2017 · However, the skewed sex ratios may be due to an environmental sex determination mechanism, such as temperature-dependent sex determination ...
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Earliest known lepisosteoid extends the range of anatomically ...
Dec 19, 2017 · Until now, the oldest known lepisosteoids were the obaichthyids, which show general neopterygian features lost or transformed in lepisosteids.Missing: classification | Show results with:classification
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Diversity of Mesozoic semionotiform fishes and the origin of gars ...
Aug 10, 2025 · Gars are the most species-rich of the two surviving lineages of Holostei, one of four major clades in the ray-finned fish tree of life ...
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New occurrences of Atractosteus (Ginglymodi: Lepisosteoidea ...
Currently, the order comprises one living family (Lepisosteidae), two genera (Lepisosteus Lacépède, 1803 and Atractosteus Rafinesque, 1820), and seven species, ...Missing: classification Wiley<|control11|><|separator|>
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Developmental cardiorespiratory physiology of the air-breathing ...
... air breathing in larval Atractosteus ... vascularization of the bladder is present. A functional aerial gas exchange organ in the form of the swim bladder ...
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Evolution of Air Breathing: Oxygen Homeostasis and the Transitions ...
Apr 1, 2013 · Life originated in anoxia, but many organisms came to depend upon oxygen for survival, independently evolving diverse respiratory systems ...
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Giant gar from directly above the Cretaceous–Palaeogene boundary ...
Phylogenetic analyses. We assessed the phylogenetic position of †Atractosteus grandei using the matrix of Grande [34] with the updates of [35] and [36]. This ...
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Genetic variation and recent population history of the tropical gar ...
Nov 28, 2008 · Apparently, the populations of this fish have decreased in size because of anthropogenic pressures, such as habitat degradation and destruction.Missing: Paleogene colonization
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Fossil Fish Species - National Park Service
Oct 10, 2025 · Fossil fishes are the most common fossils from the Fossil Butte Member (FBM). So far, 27 species of fishes have been discovered in the FBM.
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Atractosteus simplex (Leidy, 1873) - Fishes - The Fossil Forum
Mar 13, 2022 · Atractosteus simplex and A. atrox occur mainly in Fossil Lake deposits where they are relatively rare (less than 0.05% of the fish fauna).