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        First reported actinopterygian from the Navajo Sandstone (Lower Jurassic, Glen Canyon Group) of southern Utah, USA
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        First reported actinopterygian from the Navajo Sandstone (Lower Jurassic, Glen Canyon Group) of southern Utah, USA
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        First reported actinopterygian from the Navajo Sandstone (Lower Jurassic, Glen Canyon Group) of southern Utah, USA
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Abstract

We report the first occurrence of an actinopterygian fish from the Lower Jurassic Navajo Sandstone, discovered in the Grand Staircase-Escalante National Monument in southern Utah, U.S.A. The site contains multiple individuals, preserved within an interdune deposit, possessing the elongate modified dorsal scales usually characterizing semionotiform fishes. The presence of moderately sized fish provides further evidence that interdune oases were occasionally persistent environmental habitats within the greater Navajo dune system, and that the paleobiota is still woefully undersampled. Additionally, this site could help fill a gap in the actinopterygian fossil record between the patchy Lower Jurassic and better-known Middle Jurassic documentation of western North America.

Introduction

Late Triassic and Early Jurassic fish assemblages from western North America are, in part, very diverse. Assemblages in the Chinle Formation and the “Lake Dixie fauna” of the Whitmore Point Member of the Moenave Formation document an ichthyofaunal transition across the Triassic-Jurassic boundary (Milner et al., Reference Milner, Kirkland and Birthisel2006), but the remainder of the known Early Jurassic fish record in the West is rather sparse. This stands in contrast to the rich and well-documented coeval faunas from the Eastern Seaboard. Here, large lacustrine deposits have been discovered (e.g., the Newark Supergroup) with morphologically diverse assemblages of fish, chiefly composed of semionotiform taxa (Olsen et al., Reference Olsen, McCune and Thomson1982; McCune, Reference McCune1987).

Worldwide, semionotiforms were dominant and ubiquitous in aquatic ecosystems by the Late Triassic (Padian and Clemens, Reference Padian and Clemens1985; Cavin, Reference Cavin2010), and this certainly characterizes the group in the Early Jurassic “Lake Dixie fauna” (Milner and Kirkland, Reference Milner and Kirkland2006). However, the ichthyofauna from the overlying Kayenta Formation and Navajo Sandstone range from depauperate to unknown, respectively, despite the wealth of fossil tetrapods described from the Kayenta (see Sues et al., Reference Sues, Clark and Jenkins1994; Tykoski et al., Reference Tykoski, Rowe, Ketchum and Colbert2002 and references therein). Whether this biased record is a result of unequal sampling (Milner et al., Reference Milner, Kirkland and Birthisel2006) or a result of preservational or paleoenvironmental factors (Curtis and Padian, Reference Curtis and Padian1999) is debatable. Regardless, their relative rarity makes the discovery of any new fish-bearing sites in the Early Jurassic of the American West noteworthy. Here we report a new locality that has produced several semionotiform specimens from the Lower Jurassic Navajo Sandstone of Utah, representing the first known actinopterygian fossils from the entire unit. Additionally, the presence of moderately sized fish within the expansive Navajo erg system bolsters the case for persistent, deep interdune lakes (e.g., Eisenberg, Reference Eisenberg2003; Parrish and Falcon-Lang, Reference Parrish and Falcon-Lang2007) and highlights the importance of targeting interdune deposits for future field study, which will likely increase the diversity of the Navajo paleobiota (Winkler et al., Reference Winkler, Jacobs, Congleton and Downs1991).

Repository and institutional abbreviation

OMNH, Oklahoma Museum of Natural History, Norman, Oklahoma, USA.

Geologic setting

The Navajo Sandstone records an expansive Early Jurassic (Pliensbachian–Toarcian) dune system, covering much of what is now the Colorado Plateau (Fig. 1). The unit is the youngest component of the Glen Canyon Group; at its base, the Navajo intertongues with the dominantly fluvial Kayenta Formation, while the top of the unit is truncated by the J-1 unconformity where it meets the overlying Temple Cap or Carmel formations (e.g., Blakey et al., Reference Blakey, Peterson and Kocurek1988; see reinterpretation of this transition by Doelling et al., Reference Doelling, Sprinkel, Kowallis and Kuehne2013). Lithologically, the Navajo is predominantly composed of eolian sands stacked in thick sets of high-angle crossbeds. Interdune deposits are represented by localized limestones or relatively thin, horizontally bedded clastics. Periodic and occasionally prolonged shifts to a wetter climate stabilized portions of the Navajo erg and have been implicated in the formation of some of these deposits (Loope and Rowe, Reference Loope and Rowe2003), with some interdunes remaining wet enough for long enough to preserve large fossil trees (Parrish and Falcon-Lang, Reference Parrish and Falcon-Lang2007) and even giant stromatolites (Eisenberg, Reference Eisenberg2003). Similar paleontological and sedimentological indicators of wet episodes have been recorded in the laterally equivalent Nugget Sandstone in northeastern Utah (e.g., Good and Ekdale, Reference Good and Ekdale2014).

Figure 1 Map showing extent of Navajo Sandstone exposures in southwestern USA; inset shows location of OMNH V1700. Modified from Winkler et al. (Reference Winkler, Jacobs, Congleton and Downs1991).

Study of the vertebrate paleobiota of the Navajo Sandstone has understandably been focused on its ichnofauna. Vertebrate trackways are diverse and locally abundant (see summary in Irmis, Reference Irmis2005; Milàn et al., Reference Milàn, Loope and Bromley2008), and complex burrows potentially made by small mammaliaforms have also been found (Riese et al., Reference Riese, Hasiotis and Odier2011). However, some body fossils are known from the Navajo; while incomplete, most are articulated and very well preserved. Though most specimens are indeterminate below family or order, the assemblage is clearly taxonomically diverse (Irmis, Reference Irmis2005). Some specimens (at least two sauropodomorphs) were discovered in eolian sandstones: a partial skeleton first reported by Brady (Reference Brady1935, Reference Brady1936) and described later by Galton (Reference Galton1971); and the sauropodomorph Seitaad (Sertich and Loewen, Reference Sertich and Loewen2010), which was preserved in a dune-collapse deposit. The majority of body fossils, however, have been recovered from interdune deposits. These represent paleoenvironments with better preservational potential than the surrounding dunes, and likely served as beacons to concentrate animals (Winkler et al., Reference Winkler, Jacobs, Congleton and Downs1991; Irmis, Reference Irmis2005). Despite the inferred persistence and scale of some Navajo interdunes (from plant and invertebrate remains, e.g., Eisenberg, Reference Eisenberg2003; Parrish and Falcon-Lang, Reference Parrish and Falcon-Lang2007), aquatic taxa such as fish have not been described, and the known record of vertebrates is limited to tetrapods (crocodylomorphs, dinosaurs, and tritylodontids, though turtles are also yet unknown). It is unclear if this reflects a lack of suitable distribution routes between Navajo interdunes and larger surrounding bodies of water or, more likely, poor sampling.

In 2013, an OMNH field party discovered small patches of articulated fish scales in an interdune deposit within the Navajo Sandstone along the Paria River in Grand Staircase-Escalante National Monument, southern Utah (OMNH locality V1700, Fig. 1). These exposures are within the Cockscomb, a portion of the East Kaibab monocline (see Doelling et al., Reference Doelling, Blackett, Hamblin, Powell and Pollock2010). The entire section is heavily tilted and folded such that the Navajo partly overlies the stratigraphically higher Carmel Formation at their contact. The interdune deposit is positioned towards the top of the Navajo, but the contact with the Carmel has been deformed so its precise position in the section is difficult to determine. The deposit is ~5–8 m thick, and begins with a lower, structureless, dark-reddish sandstone that weathers into large, angular boulders. This is followed by a thinly laminated (5 mm beds), well-cemented purple siltstone that transitions upwards to a pale yellow, indurated but still laminated siltstone. A blocky, yellow, tabular sandstone with ~30 cm beds caps the sequence. Typical eolian sandstone beds are present above and below the interdune deposit, with fairly sharp contacts. The specimens described in this paper were recovered from the purple siltstone beds. Precise locality information is on file at the OMNH, and is available to qualified investigators upon request.

Systematic paleontology

Class Actinopterygii Klein, Reference Klein1885

Subclass Neopterygii Regan, Reference Regan1923

Order Semionotiformes Arambourg and Bertin, Reference Arambourg and Bertin1958 sensu Olsen and McCune, Reference Olsen and McCune1991

Family indeterminate

Materials

At least two partially articulated individuals composed of scales, scale impressions, and possible teeth and fin rays (OMNH 77069–77072). Isolated scales were also recovered from the same site, within a few meters laterally of the more complete material.

Occurrence

OMNH V1700, Navajo Sandstone (Lower Jurassic), ~38 km southeast of Cannonville, Kane County, Utah, USA.

Description

The material described here represents several individuals belonging to one or more indeterminate, medium-sized semionotiform species. Although we cannot exclude the possibility that these specimens represent different taxa, no obvious features (other than size) serve to differentiate them; thus, we will herein refer to them under a single moniker as the Navajo fish. Both partially articulated specimens possess an incomplete squamation composed of rhomboidal ganoid scales (Fig. 2.1–2.4). Preserved scales vary from relatively long and caudally pointed in apparent dorsal ridge scales (Fig. 2.5, 2.6), to taller than long and more rectangular in the scales of the mid-body. Isolated scales indicate that this specimen lacks a large peg and socket articulation, although a small dorsal projection and corresponding medial groove can be seen on one scale impression (Fig. 2.7, 2.8). In addition, some isolated scales possess both the rostral and rostroventral projection used by Cavin et al. (Reference Cavin, Deesri and Suteethorn2009) to diagnose isolated semionotid scales from Thailand. The rostroventral projection is nearly a third the size of the rostrodorsal process in this specimen (OMNH 69349), but other scales appear to lack this feature altogether (Fig. 2.9, 2.10). Given the lack of comprehensive scale studies for semionotid fishes, we tentatively attribute these differences to intraspecific variation between scales from varying parts of the body.

Figure 2 Semionotiform specimens recovered from OMNH V1700. (1, 2) OMNH 77070, a specimen preserving the rostrodorsal squamation, including the characteristic dorsal ridge scales (black arrow); (3, 4) OMNH 77069, mid-ventral scale pattern and possible pelvic fin rays; (5, 6) OMNH 77069, dorsal ridge scales likely from a second individual on the same slab as Figure 2.3, 2.4; (7, 8) OMNH 69349, isolated ganoid scale preserving the peg and socket joint; (9, 10) OMNH 69350, isolated ganoid scale without the peg and socket joint.

The two most complete specimens are composed of articulated scales preserved mostly as impressions with inconsistent, small occurrences of heavily mineralized scale or bone. The first specimen (OMNH 77070, Fig. 2.1, 2.2) consists of dorsal and rostral scales abutted to impressions that compare favorably to the triangular posttemporal and rounded supracleithrum of other semionotids (Olsen and McCune, Reference Olsen and McCune1991, fig. 4A). As preserved, this specimen is at least seven scales long rostrocaudally, measuring ~30 mm in length. The dorsal margin is also preserved in this specimen, typified by scales with a highly modified elongate and caudally directed spine. Moving ventrally, the scales become more poorly preserved, but appear to elongate closer to the hypothesized midline of the fish. The second specimen (OMNH 77069) is larger, with an unbroken series at least eight scales tall by seven scales long, ~50 mm in total length as preserved (Fig. 2.3, 2.4). This specimen is composed largely of tall mid-ventral scales, as well as remnants of one of the ventral fins (likely the pelvic fin). Multiple scales on the underside of the block containing this specimen belong to an additional individual. Of interest are two scales preserved with their elongate caudal processes aligned into a single ridge, representing an additional specimen bearing the characteristic semionotid dorsal ridge crest (Fig. 2.5, 2.6). The scales of all of the specimens are relatively smooth, lacking obvious large tubercles. A third block preserves what appear to be cross-sections of small, circular teeth packed in close proximity to one another. They appear to be of a crushing-style tooth morphology, which McCune (Reference McCune1986) attributed mostly to Lepidotes species, but acknowledged that this is likely size-related and exceptions do occur. The Navajo fish does not have the large humped back seen in Lophionotus sanjuanensis Gibson, Reference Gibson2013a, nor is its body greatly thickened dorsoventrally as in many other semionotiform species (e.g., Jain, Reference Jain1984; McCune, Reference McCune1986; Wenz, Reference Wenz2003). In life, this species would have been a medium-sized semionotiform, eclipsed by some of the Late Jurassic and Cretaceous species (e.g., Jain, Reference Jain1984), but substantially larger than the diminutive Lophionotus kanabensis Schaeffer and Dunkle, Reference Schaeffer and Dunkle1950 (Gibson, Reference Gibson2013b), one of the few described species of semionotids from the Western United States, which is not known to exceed 74 mm in length.

Remarks

The Navajo fish material is decidedly similar to other North American Jurassic fish, mainly of the genera Lepidotes and Semionotus (the latter of which likely represents two genera, including Lophionotus of Gibson, Reference Gibson2013a, Reference Gibson2013b, but which will be treated here as single genus for historical context); however, difficulties differentiating these genera are well documented (Schaeffer, Reference Schaeffer1967; McCune, Reference McCune1986). Precise determination of the Navajo fish species is hindered in part by the state of preservation of the few known specimens. No skull was recovered with any of the specimens, making genus- and species-level identification impossible. Nonetheless, the elongate dorsal ridge scales and scale morphology provide enough comparative material to confidently assign the order Semionotiformes. Further, given the numeric abundance of Semionotus and Lepidotes during the Early to Middle Jurassic, it would be reasonable to hypothesize that this material represents one of these taxa. Olsen and McCune (Reference Olsen and McCune1991, p. 270) condensed both genera into a restricted definition of the family Semionotidae, based on two synapomorphies: the presence of dorsal ridge scales; and a large, posteriorly directed “epiotic.” More recent phylogenetic analyses of semionotiform relationships, however, demonstrated that even this reduction is paraphyletic. Cavin (Reference Cavin2010) recovered Lepidotes and Semionotus as consecutive branches on an unnamed node nested within a monophyletic Semionotiformes. Like previous analyses, Semionotiformes has been recovered as a monophyletic group, containing Macrosemiidae, Semionotidae, and Lepisosteidae (Olsen and McCune, Reference Olsen and McCune1991; Brito, Reference Brito1997; Cavin et al., Reference Cavin, Suteethorn, Khansubha, Buffetaut and Tong2003). Cavin’s (Reference Cavin2010) phylogeny further recovers an unnamed clade within Semionotiformes to the exception of the Macrosemiidae, which can be diagnosed in part by the presence of dorsal ridge scales. This character, which is unambiguously present on the Navajo material, is highly conspicuous in most Semionotus species, but often more discreet in Lepidotes (McCune, Reference McCune1986). However, a more recent phylogenetic analysis by López-Arbarello (Reference López-Arbarello2012; corroborated by Gibson, Reference Gibson2013a, Reference Gibson2013b, Reference Gibson2016) brings into question the close relationship between Semionotus and Lepidotes. In this analysis, Lepidotes was recovered in a separate clade (order Lepisosteiformes) more similar to the modern gar (Lepisosteus Lacepède, Reference Lacepède1803 and Atractosteus Rafinesque, Reference Rafinesque1820) than to Semionotus. Semionotus was found to be monophyletic (Semionotidae), nested within a broader order Semionotiformes. The large, conspicuous dorsal ridge, used by previous authors to diagnose semionotids, was recovered in this analysis as an autapomorphy for the genus Semionotus (or a synapomorphy for Semionotidae, including both Lophionotus and Semionotus [Gibson, Reference Gibson2013b]). This split largely agrees with Grande’s (Reference Grande2010) phylogeny, where Semionotiformes and Lepisosteiformes form sister groups within the broader Ginglymodii. Without a more complete dorsal series, it is nearly impossible for us to assign the Navajo specimens to either the more Lepidotes-like Lepisosteiformes or the Semionotus-like Semionotiformes using this scheme. Given that the aforementioned taxonomic issues require a more comprehensive revaluation of the entire clade, we hesitate to delve into this debate. Here we stick to a more classic definition of Semionotiformes (sensu Olsen and McCune, Reference Olsen and McCune1991), with the understanding that more complete material will require a thorough incorporation of this species into the current ginglymodian phylogeny.

Discussion

Paleoenvironmental significance

Due to an increased risk of predation by wading predators at shallow water depths, it has been generally observed that larger fish tend to live in deeper water systems (Werner et al., Reference Werner, Hall, Laughlin, Wagner, Wilsmann and Funk1977; Schlosser, Reference Schlosser1988; Harvey and Stewart, Reference Harvey and Stewart1991). The presence of moderately sized fish in the Navajo deposits supports previous suggestions of relatively deep and possibly long-lived ponds in the Navajo dune system. Loope and Rowe (Reference Loope and Rowe2003) conservatively estimated the wet, pluvial episodes within the Navajo Sandstone may have lasted between 4,000 and 5,000 years, during which time yearly monsoons were capable of depositing up to 170 mm of rain per storm (Loope et al., Reference Loope, Rowe and Joeckel2001). These authors note that an analogous environment existed in the mid-Holocene Selima Oasis of Sudan, where wet periods reached a precipitation rate of up to 200 mm/yr causing high stands of pluvial Lake Selima to reach depths up to 17 m (Haynes, Reference Haynes1987; Haynes et al., Reference Haynes, Eyles, Pavlish, Ritchie and Rybak1989; Loope and Rowe, Reference Loope and Rowe2003). Although it is conceivable such water depths in the Navajo could have occurred, the fish material presented here can only in the broadest sense tell us that water depth was deep enough to support a small population of moderate-sized fishes for more than a single year. Some interdune deposits in the Navajo have been interpreted as fluvial in origin (Loope and Rowe, Reference Loope and Rowe2003). Because these fish must have dispersed to this particular interdune lake from some larger body of water, further work on Navajo interdune deposits may reveal more about how these localized habitats were connected during wetter periods in the Early Jurassic erg.

Implications for the Early Jurassic fossil fish record

Unlike the relatively well-documented fish assemblages of the eastern coast, Early Jurassic fishes of the western USA are incompletely known (Milner et al., Reference Milner, Kirkland and Birthisel2006, and references therein). Currently, only two formations from the Jurassic west have yielded recognizable fossil fish remains. The earliest is the Hettanginian “Lake Dixie fauna” from the Whitmore Point Member of the Moenave Formation of southwestern Utah and northwestern Arizona (Kirkland et al., Reference Kirkland, Milner, Olsen and Hargrave2014). This fauna has yielded a surprising diversity of material, including a hybodont shark, a palaeonisciform, a possible perleidiform, several semionotiforms, and at least two sarcopterygians (Milner and Kirkland, Reference Milner and Kirkland2006; Milner et al., Reference Milner, Kirkland and Birthisel2006). Semionotiforms are the numerically dominant group, with at least three known species historically recognized from the fauna (Eastman, Reference Eastman1917; Hesse, Reference Hesse1935; Schaeffer and Dunkle, Reference Schaeffer and Dunkle1950; see Milner and Kirkland, Reference Milner and Kirkland2006 and Milner et al., Reference Milner, Kirkland and Birthisel2006 for discussion of the validity of these taxa). The next oldest ichthyofauna is from the middle Sinemurian to early Pliensbachian Kayenta Formation, which contains two sharks and two dipnoans, as well as an undescribed coelacanth, semionotid, and palaeoniscoid (Curtis and Padian, Reference Curtis and Padian1999; Milner et al., Reference Milner, Kirkland and Birthisel2006, Reference Milner, Birthsel, Kirkland, Breithaup, Matthews, Lockley, Santucci, Gibson, DeBlieux, Hurlbut, Harris and Olsen2012; Frederickson and Cifelli, Reference Frederickson and Cifelli2017; personal communication, A.R.C. Milner, 2017). After these faunas, a gap in the Western Interior fossil fish record exists until the relatively diverse Middle Jurassic Sundance and Wanakah faunas (Schaeffer and Patterson, Reference Schaeffer and Patterson1984; Wilson and Bruner, Reference Wilson and Bruner2004). Schaeffer and Patterson (Reference Schaeffer and Patterson1984) described, but did not name, a species of Lepidotes among six other fish genera from the marine Sundance Formation. The Sundance Lepidotes is only known from a few fragmentary specimens, and is much rarer than the well known, but phylogenetically obscure, Hulletia and the basal teleosts Occithrissops and Todiltia. The fish occurrence described here from the Navajo Sandstone would fall into this gap, slightly after the semionotid-dominated Early Jurassic ichthyofaunas and well before the more diverse assemblages of Middle Jurassic formations.

Acknowledgments

We would like to thank A. Titus (BLM: Grand Staircase-Escalante National Monument) for his invaluable assistance with field reconnaissance. An anonymous reviewer and A. Milner (St. George Dinosaur Discovery Site, UT) improved the quality of the manuscript. Partial support for this project was provided by a National Geographic Society Waitt Grant to BD (#W266-13).

References

Arambourg, C., and Bertin, L., 1958, Super-ordre des Holostéens et des Halecostomi (Holostei et Halecostomi): Traité de Zoologie: Anatomie, Systématique, Biologie, v. 13, p. 21732203.
Blakey, R.C., Peterson, F., and Kocurek, G., 1988, Synthesis of late Paleozoic and Mesozoic eolian deposits of the Western Interior of the United States: Sedimentary Geology, v. 56, p. 3125.
Brady, L.F., 1935, Preliminary note on the occurrence of a primitive theropod in the Navajo: American Journal of Science, v. 30, p. 210215.
Brady, L.F., 1936, A note concerning the fragmentary remains of a small theropod recovered from the Navajo sandstone in northern Arizona: American Journal of Science, v. 31, p. 150.
Brito, P.M., 1997, Révision des Aspidorhynchidae (Pisces, Actinopterygii) du Mésozoïque: ostéologie, relations phylogénétiques, données environnementales et biogéographiques: Geodiversitas, v. 19, p. 681772.
Cavin, L., 2010, Diversity of Mesozoic semionotiform fishes and the origin of gars (Lepisosteidae): Naturwissenschaften, v. 97, p. 10351040.
Cavin, L., Suteethorn, V., Khansubha, S., Buffetaut, E., and Tong, H., 2003, A new Semionotid (Actinopterygii, Neopterygii) from the Late Jurassic–Early Cretaceous of Thailand: Comptes Rendus Palevol, v. 2, p. 291297.
Cavin, L., Deesri, U., and Suteethorn, V., 2009, The Jurassic and Cretaceous bony fish record (Actinopterygii, Dipnoi) from Thailand: Geological Society, London, Special Publications, v. 315, p. 125139.
Curtis, K., and Padian, K., 1999, An Early Jurassic microvertebrate fauna from the Kayenta Formation of northeastern Arizona: microfaunal change across the Triassic-Jurassic boundary: PaleoBios, v. 19, p. 1937.
Doelling, H.H., Blackett, R.E., Hamblin, A.H., Powell, J.D., and Pollock, G.L., 2010, Geology of Grand-Staircase-Escalante National Monument, Utah: Utah Geological Association Publication, v. 28, p. 193235.
Doelling, H.H., Sprinkel, D.A., Kowallis, B., and Kuehne, P.A., 2013, Temple Cap and Carmel Formations in the Henry Mountains basin, Wayne and Garfield counties: Utah Geological Association Publication, v. 42, p. 279318.
Eastman, C.R., 1917, Fossil fishes in the collection of the United States National Museum: Proceedings of the United States National Museum, v. 52, p. 235304.
Eisenberg, L., 2003, Giant stromatolites and a supersurface in the Navajo Sandstone, Capitol Reef National Park, Utah: Geology, v. 31, p. 111114.
Frederickson, J.A., and Cifelli, R.L., 2017, New Cretaceous lungfishes (Dipnoi, Ceratodontidae) from western North America: Journal of Paleontology, v. 91, p. 146161.
Galton, P.M., 1971, The prosauropod dinosaur Ammosaurus, the crocodile Protosuchus, and their bearing on the age of the Navajo Sandstone of northeastern Arizona: Journal of Paleontology, v. 45, p. 781795.
Gibson, S.Z., 2013a, A new hump-backed ginglymodian fish (Neopterygii, Semionotiformes) from the Upper Triassic Chinle Formation of southeastern Utah: Journal of Vertebrate Paleontology, v. 33, p. 10371050.
Gibson, S.Z., 2013b, Biodiversity and evolutionary history of †Lophionotus (Neopterygii: †Semionotiformes) from the Western United States: Copeia, v. 2013, p. 582603.
Gibson, S.Z., 2016, Redescription and phylogenetic placement of †Hemicalypterus weiri Schaeffer, 1967 (Actinopterygii, Neopterygii) from the Triassic Chinle Formation, southwestern United States: new insights into morphology, ecological niche, and phylogeny: PLoS ONE, v. 11, p. e0163657.
Good, T.R., and Ekdale, A.A., 2014, Paleoecology and taphonomy of trace fossils in the eolian Upper Triassic/Lower Jurassic Nugget Sandstone, northeastern Utah: Palaios, v. 29, p. 401413.
Grande, L., 2010, An empirical synthetic pattern study of gars (Lepisosteiformes) and closely related species, based mostly on skeletal anatomy. The resurrection of Holostei: Copeia, v. 2010, 871 p.
Harvey, B.C., and Stewart, A.J., 1991, Fish size and habitat depth relationships in headwater streams: Oecologia, v. 87, p. 336342.
Haynes, C.V., 1987, Holocene migration rates of the Sudano-Sahelian wetting front, Arba’in Desert, eastern Sahara, in Close, A.E., ed., Prehistory of Arid North Africa: Dallas, Southern Methodist University Press, p. 6984.
Haynes, C.V., Eyles, C.H., Pavlish, L.A., Ritchie, J.C., and Rybak, M., 1989, Holocene palaeoecology of the eastern Sahara; Selima Oasis: Quaternary Science Reviews, v. 8, p. 109136.
Hesse, C.J., 1935, Semionotus cf. gigas, from the Triassic of Zion Park, Utah: American Journal of Science, v. 29, p. 526531.
Irmis, R.B., 2005, A review of the vertebrate fauna of the Lower Jurassic Navajo Sandstone in Arizona: Vertebrate Paleontology of Arizona, Mesa Southwest Museum Bulletin, v. 11, p. 5571.
Jain, S.L., 1984, Some new observations on Lepidotes maximus (Holostei: Semionotiformes) from the German Upper Jurassic: Journal of the Palaeontological Society of India, v. 30, p. 1825.
Kirkland, J.I., Milner, A.C., Olsen, P.E., and Hargrave, J.E., 2014, The Whitmore Point Member of the Moenave Formation in its type area in Northern Arizona and its age and correlation with the section in St. George, Utah: evidence for two major lacustrine sequences, in MacLean, J.S., Biek, R.F., and Huntoon, J.E., eds., Geology of Utah’s Far South: Utah Geological Association Publication, 43, p. 321356.
Klein, E.F., 1885, Beiträge zur Bildung des Schädels der Knochenfische, 2: Jahreshefte des Vereins für Vaterländische Naturkunde in Württemberg, v. 42, p. 205300.
Lacepède, B.G.E., 1803, Histoire Naturelle des Poissons, v. 5: Paris, Plassan, 803 p.
Loope, D.B., and Rowe, C.M., 2003, Long‐lived pluvial episodes during deposition of the Navajo Sandstone: The Journal of Geology, v. 111, p. 223232.
Loope, D.B., Rowe, C.M., and Joeckel, R.M., 2001, Annual monsoon rains recorded by Jurassic dunes: Nature, v. 412, p. 6466.
López-Arbarello, A., 2012, Phylogenetic interrelationships of ginglymodian fishes (Actinopterygii: Neopterygii): PLoS ONE, v. 7, p. e39370.
McCune, A.R., 1986, A revision of Semionotus (Pisces: Semionotidae) from the Triassic and Jurassic of Europe: Palaeontology, v. 29, p. 213233.
McCune, A.R., 1987, Toward the phylogeny of a fossil species flock: semionotid fishes from a lake deposit in the Early Jurassic Towaco Formation, Newark Basin: Peabody Museum of Natural History Bulletin, v. 43, p. 1108.
Milàn, J., Loope, D.B., and Bromley, R.G., 2008, Crouching theropod and Navahopus sauropodomorph tracks from the Early Jurassic Navajo Sandstone of USA: Acta Palaeontologica Polonica, v. 53, p. 197205.
Milner, A.C., and Kirkland, J.I., 2006, Preliminary review of the Early Jurassic (Hettangian) freshwater Lake Dixie fish fauna in the Whitmore Point Member, Moenave Formation in southwest Utah: New Mexico Museum of Natural History and Science Bulletin, v. 37, p. 510521.
Milner, A.C., Kirkland, J.I., and Birthisel, T.A., 2006, The geographic distribution and biostratigraphy of Late Triassic–Early Jurassic freshwater fish faunas of the southwestern United States: New Mexico Museum of Natural History and Science Bulletin, v. 37, p. 522529.
Milner, A. R. C., Birthsel, T., Kirkland, J. I., Breithaup, B., Matthews, N., Lockley, M. G., Santucci, V. L., Gibson, S. Z., DeBlieux, D., Hurlbut, M., Harris, J. D., and Olsen, P. E., 2012, Tracking Early Jurassic dinosaurs in southwestern Utah and the Triassic-Jurassic transition: Nevada State Museum Paleontological Papers, v. 1, p. 1107.
Olsen, P.E., and McCune, A.R., 1991, Morphology of the Semionotus elegans species group from the Early Jurassic part of the Newark Supergroup of eastern North America with comments on the Family Semionotidae (Neopterygii): Journal of Vertebrate Paleontology, v. 11, p. 269292.
Olsen, P.E., McCune, A.R., and Thomson, K.S., 1982, Correlation of the early Mesozoic Newark Supergroup by vertebrates, principally fishes: American Journal of Science, v. 282, p. 144.
Padian, K., and Clemens, W.A., 1985, Terrestrial vertebrate diversity: episodes and insights, in Valentine, J., ed., Phanerozoic Diversity Patterns: Profiles in Macroevolution: Princeton, Princeton University Press, p. 4196.
Parrish, J.T., and Falcon-Lang, H.J., 2007, Coniferous trees associated with interdune deposits in the Jurassic Navajo Sandstone Formation, Utah, USA: Palaeontology, v. 50, p. 829843.
Rafinesque, C.S., 1820, Ichthyologia Ohioensis, or Natural History of Fishes Inhabiting the Ohio and Its Tributary Streams Preceded by a Physical Description of the Ohio and Its Branches: Lexington, W. O. Hunt, 90 p.
Regan, C.T., 1923, The skeleton of Lepisosteus, with remarks on the origin and evolution of the lower neopterygian fishes: Proceedings of the Zoological Society of London, v. 192, p. 445461.
Riese, D.J., Hasiotis, S.T., and Odier, G.P., 2011, Synapsid burrows and associated trace fossils in the Lower Jurassic Navajo Sandstone, southeastern Utah, U.S.A., indicates a diverse community living in a wet desert ecosystem: Journal of Sedimentary Research, v. 81, p. 299325.
Schaeffer, B., 1967, Late Triassic fishes from the western United States: Bulletin of the American Museum of Natural History, v. 135, p. 285342.
Schaeffer, B., and Dunkle, D.H., 1950, A semionotid fish from the Chinle Formation, with consdieration of its relationships: American Museum Novitates, 1457, p. 129.
Schaeffer, B., and Patterson, C., 1984, Jurassic fishes from the western United States, with comments on Jurassic fish distribution: American Museum Novitates, v. 2796, p. 186.
Schlosser, I.J., 1988, Predation risk and habitat selection by two size classes of a stream cyprinid: experimental test of a hypothesis: Oikos, v. 52, p. 3640.
Sertich, J.J.W., and Loewen, M.A., 2010, A new basal sauropodomorph dinosaur from the Lower Jurassic Navajo Sandstone of southern Utah: PLoS ONE, v. 5, p. e9789.
Sues, H.-D., Clark, J.M., and Jenkins, F.A. Jr, 1994, A review of the Early Jurassic tetrapods from the Glen Canyon Group of the American Southwest, in Frasier, N.C., and Sues, H.-D., eds., In the Shadow of Dinosaurs: Early Mesozoic Tetrapods: Cambridge, Cambridge University Press, p. 285294.
Tykoski, R.S., Rowe, T.B., Ketchum, R.A., and Colbert, E.H., 2002, Calsoyasuchus valliceps, a new crocodyliform from the Early Jurassic Kayenta Formation of Arizona: Journal of Vertebrate Paleontology, v. 22, p. 593611.
Wenz, S., 2003, Les Lepidotes (Actinopterygii, Semionotiformes) du Crétacé Inférieur (Barrémien) de Las Hoyas (Province de Cuenca, Espagne): Geodiversitas 25, p. 481499.
Werner, E.E., Hall, D.J., Laughlin, D.R., Wagner, D.J., Wilsmann, L.A., and Funk, F.C., 1977, Habitat partitioning in a freshwater fish community: Journal of the Fisheries Research Board of Canada, v. 34, p. 360370.
Wilson, M.V.H., and Bruner, J.C., 2004, Mesozoic fish assemblages of North America, in Arratia, G., and Tintori, A., eds., Mesozoic Fishes 3: Systematics, Paleoenvironments and Biodiversity: München, Verlag Dr. Friedrich Pfeil, p. 575595.
Winkler, D.A., Jacobs, L.L., Congleton, J.D., and Downs, W.R., 1991, Life in a sand sea: biota from Jurassic interdunes: Geology, v. 19, p. 889892.