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Albertonectes
Albertonectes
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Albertonectes
Temporal range: Late Cretaceous (Campanian), 73.5 Ma
Holotype skeleton (TMP 2007.011.0001)
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Chordata
Class: Reptilia
Superorder: Sauropterygia
Order: Plesiosauria
Superfamily: Plesiosauroidea
Family: Elasmosauridae
Subfamily: Elasmosaurinae
Genus: Albertonectes
Kubo et al., 2012
Type species
Albertonectes vanderveldei
Kubo et al., 2012

Albertonectes (meaning 'Alberta swimmer') is an extinct genus of large plesiosaurs that lived in North America during the Campanian stage of the Late Cretaceous period, at around 73.5 million years ago. The only known species is A. vanderveldei, described in 2012 from an almost complete postcranial skeleton discovered in 2007 near Lethbridge, in the province of Alberta, Canada. Although currently only documented from the holotype, a possible second specimen was discovered in 2015 in the same locality.

With a maximum length estimated at 12.1 metres (40 ft), Albertonectes is the longest known elasmosaurid. Like the other representatives of this group, it has a streamlined body with paddle-like limbs, a short tail, a small head, and an extremely long neck. The neck alone is estimated at around 7 meters (23 ft) long, making Albertonectes one of the animals with the longest known necks. It is also the vertebrate with the greatest number of cervical vertebrae identified to date, 76, ahead of its close relative Elasmosaurus.

Discovery and naming

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The first known specimen of Albertonectes was discovered in 2007 near the St. Mary River, near the town of Lethbridge, in southern Alberta, Canada. It was discovered unexpectedly by an excavator during ammolite mining carried out by the company Korite International Ltd. At the initial moment of the discovery, the excavator accidentally broke part of the fossils coming from the middle of the animal's trunk, including an unknown quantity of gastroliths (stomach stones). A large part of these fossils have since been noted as lost, and due to the unique character of the specimen as well as its excellent preservation, it was subsequently decided to leave it as is and not to remove any elements found there.[1][2] This specimen, since housed at the Royal Tyrrell Museum of Palaeontology and numbered as TMP 2007.011.0001, consists of an almost complete and articulated skeleton of a large plesiosaur, but the skull is missing. More precisely, it includes 132 vertebrae from the atlas-axis complex to fused tip of the tail vertebrae, a complete pectoral but an incomplete pelvic girdle, almost complete forelimbs and hindlimbs, disarticulated ribs, an abdominal rib, and at least 97 associated gastroliths. The skeleton also preserves two teeth coming from the lamniform shark Squalicorax, the few traces of grooves present on the left coracoid indicating that the specimen would have been scavenged after its death. Stratigraphically, the skeleton was exhumed in an area dating from the middle of the late Campanian of the Bearpaw Formation, a period located around 73.5 million years ago. In 2012, Japanese paleontologist Tai Kubo and his Canadian colleagues Mark T. Mitchell and Donald M. Henderson described the specimen as the holotype of a new genus and species of elasmosaurid named Albertonectes vanderveldei. The genus name Albertonectes comes from Alberta, in reference to the province where the animal was discovered, and from the Ancient Greek word νηκτός (nêktós, "swimmer"). The specific name is named in honor of Rene Vandervelde, the founder of the Korite International, the gem-mining company that discovered the holotype. Albertonectes represents the first significantly complete plesiosaur to be discovered in the Bearpaw Formation, as well as the second elasmosaurid to be identified in the same formation after Terminonatator in 2003.[1]

On November 9, 2015, it was reported to the Royal Tyrrell Museum that some articulated vertebrae were discovered in conditions similar to those previously mentioned, still near Lethbridge. Subsequently, more vertebrae were discovered by Korite workers, but due to the particularly difficult conditions in winter, the recovery of the fossils had to be done quickly. The fossils recovered consist of a partial skeleton preserving a vertebral column running from the base of the neck to the base of the tail, followed by a few articulated and disarticulated ribs. The discovery was made official the following year by Canadian paleontologist Darren H. Tanke via a summary, in which he referred this specimen as cf. Albertonectes.[3]

Description

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Diagram of a green plesiosaur next to a diver
Size compared to a human

Albertonectes has the longest neck of any elasmosaur ever discovered, which reached up to 7 metres (23 ft). The holotype, missing the skull, measures at 11.2 metres (37 ft) from the atlas-axis complex to the tip of the tail, suggesting a total body length of 11.6 metres (38 ft) with the skull.[1] In 2024, Henderson estimated its total body length up to 12.1 metres (40 ft) and its total body mass around 4.8 metric tons (5.3 short tons).[2]

Albertonectes is also unique among other elasmosaurids in having 76 neck vertebrae, a record number among elasmosaurids (and vertebrates as a whole).[4] Callawayasaurus with a similar count of 56 lacks the dumbbell-shaped articular faces that are present on the vertebrae of Vegasaurus. Additional traits rarely seen in other elasmosaurids include: a tapered front-side projection on the pubis that extends to the side beyond the acetabulum, a longitudinal ridge on the side of most neck vertebrae up to cervical 69, a clavicular arch that is wider than the adjacent front edge of the scapula, the lack of pectoral and pelvic bar, a tip of the tail that is made of seven fused tail vertebrae, and a slender humerus with a width-to-length ratio of 0.56, among other traits.

Albertonectes is known from a mature individual, as suggested by the fused neural spines and most cervical ribs to their centra, and by the only partial connection between the trochanter and the capitulum (head) of the femur, seen in TMP 2007.011.0001. Other observation also support an adult age, e.g. rough and wrinkled vertebral surfaces as well as well-developed facets and articulations on its wrist and ankle bones.[1]

Gastroliths

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Gastroliths. This area of the body had been smashed by an excavator bucket, resulting in the loss of parts of the ribs and some gastroliths.

The single known specimen of Albertonectes preserves gastroliths, 97 of which are exposed and visible. These poked out of the dorsal side of the body between the ribs, as the animal had come to lie down on the seabed on its back some time after death, the gastroliths moving into the present position through gravity as the body decayed. The largest of the visible gastroliths weighed an estimated 1.13 kg. Gastroliths were generally either disc-shaped or spherical; the former would've come from beaches and the latter from river mouths. All were composed of chert, as is the case with several other species of plesiosaurs. It is hypothesized that chert stones are specifically sought out by plesiosaurs as gastroliths for their hardness and durability.[2]

Classification

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Life restoration

In their original 2012 description, Kubo and colleagues argued that assigning Albertonectes to the Elasmosauridae would be problematic in the absence of cranial material, as the skull provides key diagnostic features for newly described species. Nevertheless, many other elasmosaurids, including the type genus Elasmosaurus, are known primarily from postcranial remains, and numerous previous cladistic analyses have shown that more than one-third of the characters used are postcranial. To determine the phylogenetic affinities of Albertonectes, the authors coded it into a data matrix originally created by Tamaki Sato in 2002. They recovered it in a relatively basal position within the Elasmosauridae, although the exclusion of cranial characters increased the number of unresolved polytomies.[1] In the official description of the related genus Vegasaurus, published in 2015, Argentine paleontologist José P. O’Gorman and colleagues adopted the modified topology proposed by Kubo et al. (2012). In this analysis, Albertonectes occupied a more derived position, within a clade that also included Futabasaurus and Mauisaurus[5]—the latter since recognized as a nomen dubium in a paper published two years later.[6]

Life reconstruction of a blue long-necked marine reptile on a white background.
Life restoration of Elasmosaurus, viewed as the sister taxon of Albertonectes according to the most recent phylogenetic analyses.

In 2016, Chilean paleontologist Rodrigo A. Otero established the subfamily Styxosaurinae to include four genera: Terminonatator, Styxosaurus, Albertonectes, and Elasmosaurus. Members of this group are primarily characterized by having more than 60 cervical vertebrae. Within the subfamily, Albertonectes and Elasmosaurus form a derived branch that includes the only known representatives with more than 70 cervical vertebrae.[7] In another analysis published the following year, American paleontologist Danielle J. Serratos and her colleagues did not resolve the position of Elasmosaurus, but noted that the Styxosaurinae could be synonymous with the Elasmosaurinae if the type genus indeed belongs to the group.[8] In 2020, O’Gorman formally synonymized the Styxosaurinae with the Elasmosaurinae based on the inclusion of Elasmosaurus within the clade, and also provided a list of diagnostic features defining it.[9] The following cladogram follows Otero (2016),[7] with clade names following O’Gorman (2020):[9]

Cryptoclidia

See also

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References

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Albertonectes is an extinct of elasmosaurid that lived during the Upper stage of the period, approximately 72 million years ago, in the marine environments of what is now western . Known from a single, nearly complete postcranial (TMP 2007.011.0001) lacking a , it represents one of the most well-preserved elasmosaurid specimens and is distinguished by possessing the longest neck among all known plesiosaurs, with 76 measuring about 7 meters in length. The total body length of the is estimated at 11.2 meters, making it one of the largest elasmosaurs. The specimen was discovered in the of , , by amateur paleontologists Mike Parks and Robin Cox in 2007, and formally described in 2012 as Albertonectes vanderveldei, honoring the discoverers' friend Levi Vandervelde. This elasmosaurid exhibits several diagnostic features, including a wide clavicular arch, a lateral longitudinal ridge on the posterior , and a slender , placing it within a derived of long-necked plesiosaurs from the middle to late . The presence of 97 gastroliths (stomach stones) in the abdominal region, ranging from less than 1 cm to 13.5 cm in diameter, suggests these were ingested to aid digestion or buoyancy control, possibly near coastal areas rich in chert pebbles. Additionally, the bone bears tooth marks from scavenging by the shark sp., indicating post-mortem predation shortly after death. As a piscivorous , Albertonectes likely inhabited the , a vast dividing at the time, where it may have foraged for soft-bodied or bottom-dwelling prey using its elongated neck, though the neck's relative stiffness suggests it was not highly flexible for rapid strikes. Its discovery highlights the diversity of elasmosaurids in the and provides insights into the evolutionary trends toward extreme neck elongation in this group, surpassing even the previously record-holding Elasmosaurus with 71 .

Discovery and naming

Geological context

The specimen of Albertonectes vanderveldei was discovered in 2007 during operations for gem-quality (fossilized ammonite shells) conducted by Korite International Ltd., south of in , . The remains were recovered from the , a predominantly marine shale unit that forms part of the Upper Cretaceous succession in the Western Canadian Sedimentary Basin. The dates to the upper stage of the , corresponding to an age of approximately 74.3–73.1 million years ago. This formation records the final major marine incursion of the , a shallow epicontinental sea that periodically flooded the North American interior during the . The was characterized by low-energy, open-marine conditions during a transgressive phase, with sediments primarily consisting of dark gray to black shales interbedded with layers ( deposits) and minor thin sandstones, indicative of quiet offshore waters with periodic sediment input from volcanic activity and distant shorelines.

Etymology and type material

The genus name Albertonectes is derived from "," referring to the Canadian province where the was discovered, combined with word nêktês, meaning "swimmer," in reference to its marine lifestyle. The species name vanderveldei honors the late René Vandervelde, founder of Korite International, the mining company whose operations led to the discovery of the specimen. The specimen, cataloged as TMP 2007.011.0001, consists of an almost complete postcranial skeleton collected in 2007. It is missing only the , the left , and some distal elements of the hind limbs, preserving 76 vertebrae, a partial pectoral girdle, both pelvic girdles, and most of the limb elements. This specimen was formally described and named in 2012 by Tai Kubo, Mark T. Mitchell, and Donald M. Henderson in the Journal of Vertebrate Paleontology. It is housed at the Royal Tyrrell Museum of Palaeontology in Drumheller, , .

Description

Overall morphology

Albertonectes vanderveldei was a large elasmosaurid , estimated to have reached a total body length of 12.1 meters (40 feet) and a mass of approximately 4.8 metric tons based on volumetric reconstructions. The animal exhibited a streamlined characteristic of advanced elasmosaurids, adapted for efficient aquatic in the . This included a proportionally small head, inferred from the overall skeletal proportions preserved in the specimen, a markedly elongated , a robust and compact torso supported by broad ribs, four well-developed paddle-like limbs serving as primary propulsive structures, and a relatively short tail that contributed minimally to overall length. The limb girdles and appendages were specialized for subaqueous locomotion, featuring hyperphalangy in the digital rows of the paddles, which increased the surface area for generation. Propodials (humeri and femora) were elongated and robust, providing leverage, while epipodials (radii, ulnae, tibiae, and fibulae) were similarly extended and broadened to facilitate the expansive, wing-like motion typical of swimming. These adaptations underscored the animal's reliance on undulatory and oscillatory limb movements for propulsion in marine environments. The general body proportions highlighted the neck's dominance, comprising about 58% of the total length and underscoring its central role in the ’s morphology, with the preserving a record number of that further accentuates this feature (detailed in the section).

Axial skeleton

The axial skeleton of Albertonectes vanderveldei is characterized by an exceptionally high total vertebral count, including 76 , 22 dorsal vertebrae, 5 sacral vertebrae, and 33 caudal vertebrae. This configuration underscores the extreme elongation typical of elasmosaurid plesiosaurs, with the postcranial skeleton preserved nearly completely in the type specimen (TMP 2007.011.0001). The , numbering 76, represent the greatest number known among all vertebrates, surpassing the 71 cervicals of its close relative platyurus and exceeding counts in other elasmosaurids such as (typically 50–60). This record-breaking series results in a neck length of approximately 7 meters (23 feet), comprising over half the animal's estimated total body length of 12.1 meters. The cervical centra are notably elongated and shallowly amphicoelous, featuring low neural arches, prominent lateral longitudinal ridges on the posterior elements, and ventral notches; their size increases gradually from anterior to posterior, enhancing overall neck extension without abrupt transitions. The dorsal vertebrae, totaling 22, exhibit shorter compared to the cervicals, with the anterior ones retaining a ventral notch similar to the neck region; neural spines are damaged in the but indicate a relatively short trunk. The 5 sacral vertebrae articulate closely with the ilia, supporting the pelvic in a manner consistent with elasmosaurid adaptations for aquatic locomotion. The 33 caudal vertebrae form a short tail, with the distal elements showing chevron facets and reduced haemal arches, tapering to a fused tip that contributes minimally to propulsion. This vertebral arrangement, particularly the profuse cervical count, implies adaptations for greater flexibility and reach in open marine habitats, allowing Albertonectes to access prey at extended distances while maintaining a streamlined body profile.

Gastroliths

Ninety-seven were preserved in the abdominal region of the specimen of Albertonectes vanderveldei, visible within the articulated postcranial skeleton. These stones, primarily composed of chert, ranged in size from small pebbles with diameters less than 1 cm to larger examples up to approximately 14 cm in diameter. The largest individual gastrolith weighed an estimated 1.13 kg. The gastroliths were clustered in the gut area, suggesting they were ingested intentionally by the animal rather than displaced post-mortem. Their total estimated mass was approximately 9.3 kg, representing less than 0.2% of the animal's body mass. This arrangement and quantity indicate the stones served functions such as grinding ingested food in the or aiding control, particularly useful for a piscivorous diet involving the of bones and scales. The preservation of these gastroliths is notable, as the high degree of articulation in the allows for their direct association with the digestive tract of A. vanderveldei, providing rare insight into plesiosaurian gastric processes.

Classification

Systematic placement

Albertonectes is classified within the kingdom Animalia, phylum Chordata, class Reptilia, order Plesiosauria, family Elasmosauridae, and subfamily Elasmosaurinae. The genus is monotypic, containing only the Albertonectes vanderveldei, named and described in 2012 based on a nearly complete postcranial from the in , . Upon its initial description, Albertonectes vanderveldei was placed within Elasmosauridae due to shared features such as an extremely elongated neck comprising 76 —the highest count known among plesiosaurs—and other postcranial characteristics aligning with elasmosaurids. Its assignment to the subfamily Elasmosaurinae is supported by the extreme neck length, the shape of mid- (elongated and can-shaped), and vertebral features like lateral longitudinal ridges on the posterior cervicals, which distinguish it from earlier elasmosaurids with shorter necks. Members of Elasmosauridae are diagnosed by extreme elongation of the neck (often over 60 ), a relatively small with long, slender, interlocking teeth, and limbs modified into broad, paddle-like flippers for in marine environments. These traits reflect adaptations for a piscivorous in open ocean settings during the .

Phylogenetic relationships

Albertonectes vanderveldei is positioned as a derived member of the Elasmosauridae, specifically within the subfamily Elasmosaurinae, which has been synonymized with Styxosaurinae in several cladistic analyses of plesiosaurs. This placement reflects its occurrence among long-necked elasmosaurids from the during the stage, highlighting a late phase of diversification in this group. Early phylogenetic assessments, such as the preliminary analysis in its original description, confirmed its inclusion in a of middle to elasmosaurids characterized by extreme neck elongation, using a modified derived from prior studies on sauropterygian relationships. Subsequent revisions have refined its interrelationships, identifying Albertonectes as the sister taxon to platyurus and part of a more inclusive that also encompasses and Libonectes. This topology emerges from expanded cladistic matrices, including the comprehensive plesiosaur phylogeny of Druckenmiller and Russell (2008), which analyzed 152 postcranial and cranial characters across Plesiosauria, and the faunal turnover study by Benson and Druckenmiller (2014), incorporating 243 characters to resolve elasmosaurid ingroup relationships with improved resolution. For instance, a 2016 reassessment of using a modified version of the Benson and Druckenmiller (2014) matrix recovered Styxosaurinae (including Albertonectes, , Terminonatator, and ) with 87% bootstrap support, emphasizing its derived status among North American elasmosaurids. The phylogenetic position of Albertonectes is supported by key autapomorphic and synapomorphic characters, notably its exceptionally high cervical vertebral count of 76, exceeding that of most elasmosaurids and aligning it with the extreme neck elongation seen in its closest relatives, as well as a specific phalangeal formula in the paddles (e.g., elongated propodials and reduced hyperphalangy). These traits, evaluated in the 20-character analysis of Kubo et al. (2012) and corroborated in broader datasets, underscore its role in the terminal diversification of long-necked plesiosaurs, contributing to the of elasmosaurids in epicontinental seaways during the final stages of the . This positioning implies that such specialized morphologies persisted until near the end of the , with Albertonectes representing one of the geologically youngest well-known elasmosaurids from the .

Paleobiology

Diet and feeding

Albertonectes vanderveldei was primarily piscivorous, with a diet inferred to consist mainly of small , based on the characteristic anatomy of elasmosaurids, which includes a small head relative to body size and an exceptionally long neck adapted for pursuing agile prey in open water. The absence of the in the known specimen limits direct evidence, but elasmosaurid typically features slender, conical teeth suited for piercing and grasping soft-bodied prey like , rather than crushing harder items. The presence of 97 gastroliths—polished chert stones recovered from the abdominal region of the —further supports this, as such stones have been hypothesized to aid in mechanically grinding ingested bones and scales within the stomach, though their exact function remains debated and may also include buoyancy control. The gastroliths imply a feeding focused on soft-bodied marine organisms, such as or squid, excluding diets heavy in hard-shelled mollusks or crustaceans that would require different digestive adaptations. Stomach contents from related elasmosaurids confirm this niche, with preserved remains (e.g., and other small teleosts) indicating opportunistic predation on schooling in the . Albertonectes likely employed an ambush or pursuit tactic, maintaining a straight neck during steady swimming and using primarily ventral flexion—given the neck's relative stiffness—to position the head for prey capture, leveraging its 76 for extended reach without repositioning the body. In the shallow inland sea of the Bearpaw Formation, Albertonectes filled a top marine predatory role, specializing in a narrow piscivorous niche amid diverse vertebrate assemblages. This position suggests potential dietary overlap and competition with large mosasaurs like Tylosaurus, which shared similar elemental signatures indicative of fish- or squid-based diets in the same environment.

Locomotion and habitat

Albertonectes vanderveldei, like other elasmosaurid plesiosaurs, propelled itself through the water primarily using its four paddle-like flippers, which functioned as hydrofoils to generate thrust through oscillatory movements. The foreflippers were larger than the hind ones and served as the primary propulsors, while the hind flippers contributed significantly to overall efficiency, producing up to 60% more thrust when synchronized with the foreflippers in a coordinated swimming motion. The tail, though short, provided secondary propulsion through undulatory motions and aided in steering during travel. The exceptionally long neck, composed of 76 , offered flexibility primarily in ventral bending, enabling maneuvering in aquatic environments and potentially assisting in subtle adjustments for depth changes or orienting the head to detect prey via visual cues from below. This flexibility was complemented by the ability to stiffen the neck during straight-line swimming, integrating it into the overall streamlined body for efficient locomotion. Albertonectes inhabited the shallow to mid-depth waters of the during the upper stage of the , a period marked by into central that formed the Bearpaw Sea. The , where its fossils were discovered, records deposition in shallow marine conditions adjacent to a deltaic system. Key adaptations for fully aquatic life included lightweight, low-density bones exhibiting osteoporotic-like microanatomy, which reduced overall body weight to enhance control without compromising structural integrity. Additionally, the presence of 97 chert gastroliths in the abdominal region likely served as to fine-tune and position in the , complementing deflation for diving, though their role is debated and may also include aiding . As a fully marine species with no evidence of terrestrial interactions, Albertonectes probably led a pelagic lifestyle, migrating to follow seasonal prey distributions within the seaway.

References

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