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Hanson Formation
Hanson Formation
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The Hanson Formation (also known as the Shafer Peak Formation) is a geologic formation on Mount Kirkpatrick and north Victoria Land, Ross Dependency, Antarctica. It is one of the two major dinosaur-bearing rock groups found on Antarctica to date; the other is the Snow Hill Island Formation and related formations from the Late Cretaceous of the Antarctic Peninsula. The formation has yielded some Mesozoic specimens, but most of it is as yet unexcavated. Part of the Victoria Group of the Transantarctic Mountains, it lies below the Prebble Formation and above the Falla Formation.[2] The formation includes material from volcanic activity linked to the Karoo-Ferar eruptions of the Lower Jurassic.[3][4] The climate of the zone was similar to that of modern southern Chile, humid, with a temperature interval of 17–18 degrees.[5] The Hanson Formation is correlated with the Section Peak Formation of the Eisenhower Range and Deep Freeze Range, as well as volcanic deposits on the Convoy Range and Ricker Hills of southern Victoria Land.[2] Recent work has successfully correlated the Upper Section Peak Formation, as well unnamed deposits in Convoy Range and Ricker Hills with the Lower Hanson, all likely of Sinemurian age and connected by layers of silicic ash, while the upper section has been found to be Pliensbachian, and correlated with a greater volcanic pulse, marked by massive ash inputs.[6][7]

Key Information

History

[edit]
Map showing location of the Mount Kirkpatrick dinosaur site, with stratigraphic context of the Hanson Formation

The Victoria Group (also called Beacon Supergroup) from the Central Transantarctic Mountains was defined by Ferrar in 1907, when he described the "Beacon Sandstone" of the sedimentary rocks in the valleys of the Victoria Land.[8] Following this initial work, the term "Beacon System" was introduced for a series of similar sandstones and associated deposits that were recovered locally.[9] Later the "Beacon Sandstone Group" was assigned to those units in Victoria Land, with Harrington in 1965 proposing the name for different units that appear in the Beacon rocks of south Victoria Land, the beds below the Maya erosion surface, the Taylor Group and the Gondwana sequence, including the Victoria Group.[10] This work left out several older units, such as the Permian coal measures and glacial deposits.[10] It was not until 1963 that there was an establishment of the Gondwana sequence: the term Falla Formation was chosen to delimit a 2300 ft (700 m) series of lower quartz sandstone, a middle mica-carbon sandstone and an upper sandstone-shale unit.[11] The formation lying above the Falla Formation and below the Prebble Formation was then termed the Upper Falla Formation, with considerable uncertainty about its age (it was calculated from the presence of Glossopteris-bearing beds (Early Permian) and the assumed possibility that the rocks were older than Dicroidium-bearing beds, thought to be Late Triassic, in the Dominion Range).[12] Later works tried to set it between the Late Triassic (Carnian) and the Lower-Middle Jurassic (ToarcianAalenian).[13] The local Jurassic sandstones were included in the Victoria Group, with the Beacon unit defined as a supergroup in 1972, comprising beds overlying the pre-Devonian Kukri erosion surface to the Prebble Formation in the central Transantarctic Mountains and the Mawson Formation (and its unit, then separated, the Carapace Sandstone) in southern Victoria Land.[14] The Mawson Formation, identified at the beginning as indeterminate tillite, was later placed in the Ferrar Group.[15]

Extensive fieldwork later demonstrated the need for revisions to the post-Permian stratigraphy.[16] It was found that only 282 m of the upper 500 m of the Falla Formation as delimited in 1963 correspond to the sandstone/shale sequence, with the other 200 m comprising a volcaniclastic sequence.[16] New units were then described from this location: the Fremouw Formation and Prebble Formation, the latter term being introduced for a laharic unit, not seen in 1963, that occurs between the Falla Formation and the Kirkpatrick Basalt.[16][17] A complete record was recovered at Mount Falla, revealing the sequence of events in the Transantarctic Mountains spanning the interval between the Upper Triassic Dicroidium-bearing beds and the Middle Jurassic tholeiitic lavas.[16] The upper part of the Falla Formation contains recognizable primary pyroclastic deposits, exemplified by resistant, laterally continuous silicic tuff beds, that led this to be considered a different formation, especially as it shows erosion associated with tectonic activity that preceded or accompanied the silicic volcanism and marked the onset of the development of a volcano-tectonic rift system.[2]

The Shafer Peak Formation was named from genetically identical deposits from north Victoria Land (exposed on Mt. Carson) in 2007 and correlated with the Hanson Formation, defined as tuffaceous deposits with silicic glass shards along with quartz and feldspar.[18] Later works, however, have equated it to a continuation of the Hanson Formation, as part of the upper member.[6]

The name "Hanson Formation" was proposed for the volcaniclastic sequence that was described in Barrett's 1969 Falla Formation essay.[16] The name was taken from the Hanson Spur, which lies immediately to the west of Mount Falla and is developed on the resistant tuff unit described below.[2]

Paleoenvironment

[edit]
Environment reconstruction of the Hanson Formation with a Plinian eruption in the background

The Hanson Formation accumulated in a rift environment located between c. 60 and 70S, fringing the East Antarctic Craton behind the active Panthalassan margin of southern Gondwana, being dominated by two types of facies: coarse- to medium-grained sandstone and tuffaceous rocks & minerals on the fluvial strata, which suggest the deposits where influenced by a large period of silicic volcanism, maybe more than 10 million years based on the thickness.[19] When looking at the composition of this tuffs, fine grain sizes, along others aspects such as bubble-wall and tricuspate shard form or crystal-poor nature trends to suggest this volcanic events developed as distal Plinian Eruptions (extremely explosive eruptions), with some concrete layers with mineral grains of bigger size showing that some sectors where more proximal to volcanic sources.[19] The distribution of some tuffs with accretionary lapilli, found scattered geographically and stratigraphically suggest transport by ephemeral river streams, as seen in the Oruanui Formation of New Zealand.[19] The sandstones where likely derived of low-sinuosity sandybraided stream deposits, having interbeds with multistory cross-bedded sandstone bodies, indicators of either side channels or crude splay deposits and concrete well-stratified sections representing overbank deposits and/or ash recycled by ephemeral streams or aeolian processes.[19] Towards the upper layers of the formation the influence of the Tuff in the sandstones get more notorious, evidenced by bigger proportions of volcanic minerals and ash-related materials embedded in between this layers. Overall, the unit deposition bear similarities to the several-hundredmetres-thick High Plains Cenozoic sequence of eastern Wyoming, Nebraska and South Dakota, with the fine-grained ash derived from distal volcanoes.[19]

The Shafer Peak section flora is the typical reported in warm climates. Compared with the underlying Triassic layers, warm and overall humid, possibly more strongly seasonal, specially notorious by the abundance of Cheirolepidiaceae pollen, a key thermophilic element. Yet the dominance of this pollen doesn't indicate proper dry conditions, as for example mudcrack and other indicators of strong dry seasons are mostly absent, while common presence of the invertebrate ichnogenus Planolites indicates the local fluvial, alluvial or lacustrine waters where likely continuous all year, as well the presence of abundant Otozamites trends to suggest high humidity.[20] Overall points to frost-free setting with strong seasonality in day-length given the high latitude, perhaps similar to warm-temperate, frost-free forest and open woodland as in North Island of New Zealand. Despite the proper conditions, peat accumulation was rare, mostly due to the influence of local volcanism, with common wildfire activity as show charred coalified plant remains.[20] At Mount Carson associations of sphenophyte rhizomes and aerial stems, as well isoetalean leaves suggest the presence of overbank deposits that were developed in ephemeral pools that lasted enough to be colonized by semiaquatic plants.[20]

Tectonically, based on the changes seen in the sandstone composition and the appearance of volcanic strata indicates the end of the so-called foreland depositional section in the Transantarctic Mountains, while appearance of arkoses with angular detritus and common Garnet points to local Palaeozoic basement uplift.[13] The Rift Valley deposition is recovered in several coeval and underlying points, with its thickness as indicator of palaeotopographical confinement of palaeoflows coming generally to the NW quadrant, creating a setting that received both sediment derived from the surrounding rift shoulders and ash from distal eruptions.[21] The Main fault indicator of this rift has been allocated around the Marsh Glacier, with the so-called Marsh Fault that breaks apart Precambrian rocks and the Miller Range, with other faults including a W-facing monocline that lies parallel and east of the Marsh Fault, a NW–SE-striking small graben in the southern Marshall Mountains, the fault at the Moore Mountains, the undescribed monocline facing east in the Dominion Range and an uplifted isolated fault in the west of Coalsack Bluff.[13] Marsh Fault was likely active during the early Jurassic, leading to a development of an extensive rift valley system several thousand kilometres long along which basaltic magmatism was focused later towards the Pliensbachian, when the Hanson Formation deposited, somehow similar to East African Rift Valleys and specially Waimangu Volcanic Rift Valley, with segmentation in the rift and possible latter reverse faulting.[19]

Fungi

[edit]
Color key
Taxon Reclassified taxon Taxon falsely reported as present Dubious taxon or junior synonym Ichnotaxon Ootaxon Morphotaxon
Notes
Uncertain or tentative taxa are in small text; crossed out taxa are discredited.
Genus Species Location Material Notes Images

Fungi[22][23]

Indeterminate

  • Mount Carson
  • Suture Bench
  • Fungal remains in microbial mats
  • Tylosis formation and fungi in wood
  • Type A represent Fungal remains linked to matrix microbial maths
  • Type B includes Parasitic Fungus of uncertain relationships, found associated with fossil wood allowing the formation of Tylosis
Wood decay fungus

Paleofauna

[edit]

The first dinosaur to be discovered from the Hanson Formation was the predator Cryolophosaurus, in 1991; it was formally described in 1994. Alongside these dinosaur remains were fossilized trees, suggesting that plant matter had once grown on Antarctica's surface before it drifted southward. Other finds from the formation include tritylodonts, herbivorous mammal-like reptiles and crow-sized pterosaurs. Surprising was the discovery of prosauropod remains, which were found commonly on other continents only until the Early Jurassic. However, the bone fragments found in the Hanson Formation were dated to the Middle Jurassic, millions of years later. In 2004, paleontologists discovered partial remains of a large sauropod dinosaur that has not yet been formally described.

Arthropoda

[edit]

At southwest Gair Mesa the basal layers represent a lake shore and are characterised by the noteworthy preservation of some arthropod remains.[24]

Taxon Species Location Material Notes Images

Blattodea[24]

Indeterminate

  • Southwest Gair Mesa

Complete specimen

Indeterminate Cockroach material

Coleoptera[24]

Indeterminate (various)

  • Mount Carson
  • Shafer Peak

Isolated elytron

Indeterminate beetle remains

Conchostraca[24]

Indeterminate (various)

  • Mount Carson
  • Shafer Peak
  • Suture Bench
  • Southwest Gair Mesa

Isolated valves

Numerous conchostracan remains, found associated with lagoonar deposits and major indicators of water bodies locally along Scoyenia burrows

Diplichnites[24]

D. isp.

  • Mount Carson
  • Shafer Peak

Trace fossils

Trace fossils in lacustrine environment, probably made by arthropods (arachnids or myriapods)

Diplichnites

Euestheria[25]

  • E. juravariabalis
  • Mauger Nunatak

Isolated valves

A clam shrimp (“conchostracan”), member of the family Lioestheriinae.

Lioestheria[25]

  • L. longacardinis
  • L. maugerensis
  • Mauger Nunatak

Isolated valves

A clam shrimp (“conchostracan”), member of the family Lioestheriinae.

Ostracoda[24]

Indeterminate (various)

  • Southwest Gair Mesa

Isolated valves

Numerous ostracodan remains, found associated with lagoonar deposits and indicators of water bodies locally along Scoyenia burrows and conchostracans

Palaeolimnadia[25]

  • P. glenlee
  • Storm Peak
  • Mauger Nunatak

Isolated valves

A clam shrimp (“conchostracan”), member of the family Limnadiidae.

Planolites[20]

P. isp.

  • Mount Carson
  • Shafer Peak
  • Suture Bench

Burrows

Burrow fossils in lacustrine environment, probably made by arthropods. Common Planolites burrows on bedding planes document high water tables locally, as well humid atmospheric conditions

Planolites

Scoyenia[24]

S. isp.

  • Mount Carson
  • Shafer Peak
  • Suture Bench

Burrows

Burrow fossils in lacustrine environment, probably made by arthropods

Synapsids

[edit]
Taxon Species Location Material Notes Images

Tritylodontidae[26][27][28]

Indeterminate Mt. Kirkpatrick

An isolated upper postcanine tooth, FMNH PR1824

A cynodont, incertae sedis within Tritylodontidae. It is believed to be related to the Asian genus Bienotheroides.[27] One of the largest member of the family.[27]

Tritylodon, example of Tritylodontidae

Pterosaurs

[edit]
Taxon Species Location Material Notes Images

Dimorphodontidae?[26][29][30]

Indeterminate Mt. Kirkpatrick

Humerus

A pterosaur. Nearly the same size as YPM Dimorphodon. Its morphotype is common for basal pterosaurs, such as those in Preondactylus or Arcticodactylus.

Dimorphodon, an example of a dimorphodontid

Dinosaurs

[edit]
Taxon Species Location Material Notes Images

Coelophysidae?[26][31]

Indeterminate

Mt. Kirkpatrick

Maxilla fragment with 3 teeth

Described as "halticosaurid teeth"

Coelophysis, an example of coelophysid

Cryolophosaurus[29][32]

C. ellioti

Mt. Kirkpatrick

  • FMNH PR1821: nearly complete skull and associated partial skeleton
  • Remains of a second specimen collected in 2010[33]
  • Juvenile teeth[34]

Incertae sedis within Neotheropoda, probably related to the Averostra. It is the best characterized dinosaur found in the formation, and was probably the largest predator on the ecosystem.[35]

Mounted skeleton of Cryolophosaurus
Glacialisaurus[36][37][28] G. hammeri Mt. Kirkpatrick FMNH PR1823, a partial right astragalus, medial and lateraldistal tarsals, and partial right metatarsus preserved in articulation with each other. A Distal left femur, FMNH PR1822, was referred A Sauropodomorph, member of the family Massospondylidae. Related to Lufengosaurus of China. Was recently compared with Lamplughsaura.[38]
Glacialisaurus holotype
Massopoda[39][40] Indeterminate Mt. Kirkpatrick Several vertebrae and Pelvic material Was first exhibited at the Natural History Museum of Los Angeles County, where it was compared to Leonerasaurus.[40][38]
Material of the unnamed Massopodan
Massospondylidae[39][40][41] Gen et sp. nov. Mt. Kirkpatrick FMNH PR 3051, nearly complete juvenile skeleton including partial skull Represents the only current Sauropodomorph with cranial material from the continent. Was originally compared to Leonerasaurus, yet latter was found to be related with Ignavusaurus and Sarahsaurus.[40][38]
Skull of the unnamed Sauropodomorph

Neotheropoda[26][31]

Indeterminate

Mt. Kirkpatrick

6 isolated teeth

Described as "dromeosaurid? teeth", it is probably either a Tachiraptor-grade averostra, a Coelophysis-like form, or possibly even a basal tetanuran

Ornithischia?[42][43][39] Indeterminate Mt. Kirkpatrick Dorsal vertebrae, femur and possible caudal vertebrae Described as a "four or five-foot ornithischian or bird-hipped dinosaur, is on its way back to the United States in about 5,000 pounds of rock."[43]
Eocursor, close en paleogeographical range
Sauropoda?[44][28][45] Indeterminate Mt. Kirkpatrick Three metre-wide pelvis, Ilium, isolated Vertebrae and Limb elements The presence of Glacialisaurus in the Hanson Formation with advanced true sauropods shows that both basal and derived members of this lineage existed side by side in the Early Jurassic.[36][37][44]
Ledumahadi close in paleogeographical range

Flora

[edit]

Fossilized wood is also present in the Hanson Formation, near the stratigraphic level of the tritylodont locality. It has affinities with the Araucariaceae and similar kinds of conifers.[46] In the north Victoria Land region, plant remains occur at the base of the lacustrine beds directly underlying the initial pillow lavas at the top of the sedimentary profile. Some of the layers of Shafer Peak include remains of an in situ stand gymnosperm trees:

  • At Mount Carson, at least four large tree trunks were found on an exposed bedding plane. The wood is coalified and only partially silicified, with the largest stem reaching a diameter of nearly 50 cm.[24]
  • In Suture Bench, silicified tree trunks are found buried in situ along lava flows. Some specimens have several holes or tunnels less than 1 cm wide that may represent arthropod borings.[24]

Palynology

[edit]

Likely that (at least parts of) the palynomorph contents of these samples may derive from accessory clasts of underlying host strata that were incorporated and reworked during hydrovolcanic activity[47]

Genus Species Location Material Notes

Alisporites[48]

  • A. grandis
  • A. lowoodensis
  • A. similis
  • Shafer Peak

Pollen

Affinities with the families Caytoniaceae, Corystospermaceae, Peltaspermaceae, Umkomasiaceae and Voltziaceae

Aratrisporites[48]

  • A. sp.
  • Shafer Peak

Spores

Affinities with Pleuromeiales. The Plueromeiales were tall lycophytes (2 to 6 m) common in the Triassic. These spores probably reflect a relict genus.

Araucariacites[48]

  • A. australis
  • Shafer Peak

Pollen

Affinities with the family Araucariaceae. By the Pliensbachian, Cheirolepidiaceae reduce their abundance, with coeval proliferation of the Araucariaceae-type pollen

Baculatisporites[48]

  • B. comaumensis
  • Shafer Peak

Spores

Affinities with the family Osmundaceae. Near fluvial current ferns, related to the modern Osmunda regalis.

Calamospora[48]

  • C. tener
  • Shafer Peak

Spores

Affinities with the Calamitaceae. Horsetails, herbaceous flora characteristic of humid environments and tolerant of flooding.

Classopollis[7]

  • C. cf. chateaunovi
  • C. meyerianus
  • McLea Nunatak, Prince Albert Mountains

Pollen

Affinities with the family Cheirolepidiaceae. Most samples yield well-preserved pollen and spore assemblages strongly dominated (82% and 85%, respectively, for the two species) by Classopollis grains.[7]

Corollina[48]

  • C. torosa
  • C. simplex
  • Shafer Peak

Pollen

Affinities with the family Cheirolepidiaceae. The dominance of Corollina species is the defining feature of the Corollina torosa abundance zone.

Cyathidites[48]

  • C. australis
  • Shafer Peak

Spores

Affinities with the family Cyatheaceae or Adiantaceae.

Cybotiumspora[48]

  • C. junta
  • C. jurienensis
  • Shafer Peak

Spores

Affinities with the family Cibotiaceae.

Dejerseysporites[48]

  • D. verrucosus
  • Shafer Peak

Spores

Affinities with the Sphagnaceae. Sphagnum-type swamp mosses. Aquatic in temperate freshwater swamps.

Densoisporites[48]

  • D. psilatus
  • Shafer Peak

Spores

Affinities with the Selaginellaceae.

Dictyophyllitides[48]

  • D. bassis
  • Shafer Peak

Spores

Affinities with the family Schizaeaceae, Dicksoniaceae or Matoniaceae.

Neoraistrickia[48]

  • N. tavlorii
  • N. truncaia
  • N. suratensis
  • Shafer Peak

Spores

Affinities with the Selaginellaceae.

Nevesisporites[7]

  • N. vallatus
  • McLea Nunatak, Prince Albert Mountains
  • Shafer Peak

Spores

Affinities with Bryophyta. Younger index taxa (e.g., N. vallatus) are mostly absent and the proportion of Classopollis is still very high.[7]

Perinopollenites[48]

  • P. elatoides
  • Shafer Peak

Pollen

Affinities with the family Cupressaceae.

Platysaccus[48]

  • P. queenslandii
  • Shafer Peak

Pollen

Affinities with the families Caytoniaceae, Corystospermaceae, Podocarpaceae and Voltziaceae.

Podosporites[7]

  • P. variabilis
  • McLea Nunatak, Prince Albert Mountains
  • Shafer Peak

Pollen

Affinities with the family Podocarpaceae. Occasional bryophyte and lycophyte spores are found along with consistent occurrences of Podosporites variabilis.[7]

Polycingulatisporites[48]

  • P. mooniensis
  • P. triangularis
  • Shafer Peak

Spores

Affinities with the family Notothyladaceae. Hornwort spores.

Puntactosporites[48]

  • P. walkomi
  • P. scabratus
  • Shafer Peak

Spores

Uncertain peridophyte affinities

Retitriletes[7][48]

  • R. semimuris
  • R. austroclavatidites
  • R. rosewoodensis
  • R. clavatoides
  • McLea Nunatak, Prince Albert Mountains

Spores

Affinities with the family Lycopodiaceae. Absent in some samples.[7]

Rogalskaisporites[48]

  • R. cicatricosus
  • Shafer Peak

Spores

Uncertain peridophyte affinities

Rugulatisporites[48]

  • R. nelsonensis
  • Shafer Peak

Spores

Affinities with the family Osmundaceae.

Sculptisporis[48]

  • S. moretonensis
  • Shafer Peak

Spores

Affinities with the Sphagnaceae.

Stereisporites[48]

  • S. antiquasporites
  • Shafer Peak

Spores

Affinities with the Sphagnaceae.

Trachysporites[48]

  • T. fuscus
  • Shafer Peak

Spores

Uncertain peridophyte affinities

Thymosphora[48]

  • T. ipsviciensis
  • Shafer Peak

Spores

Uncertain peridophyte affinities

Verrucosisporites[48]

  • V. varians
  • Shafer Peak

Spores

Uncertain peridophyte affinities

Vitreisporites[48]

  • V. signatus
  • Shafer Peak

Pollen

Affinities with the family Caytoniaceae.

Macroflora

[edit]
Genus Species Location Material Notes Images

Allocladus[20]

Indeterminate
  • Mount Carson

Cuticles

A member of the Pinales of the family Cheirolepidiaceae or Araucariaceae.

Cladophlebis[49][50]

  • C. oblonga
  • Carapace Nunantak (reworked)
  • Shafer Peak

Leaves and stems

A Polypodiopsidan of the family Osmundaceae. Reworked from the Hanson Formation to the Mawson Formation; represents fern leaves common in humid environments.

Example of Cladophlebis specimen

Clathropteris[20][51]

  • C. meniscoides
  • Shafer Peak
  • Mount Carson

Leaf segments

A Polypodiopsidan of the family Dipteridaceae. It was the first record of the genus and species from the Antarctica. Specimens from Shafer Peak occur in a tuffitic mass-flow deposit and are associated with abundant charred wood indicating wildfires.[51]

Example of Clathropteris specimen

Coniopteris[20]

  • C. murrayana
  • C. hymenophylloides
  • Mount Carson

Pinna fragments

A Polypodiopsidan of the family Polypodiales. Common cosmopolitan Mesozoic fern genus. Recent research has reinterpreted it a stem group of the Polypodiales (Closely related with the extant genera Dennstaedtia, Lindsaea, and Odontosoria).[52]

Cycadolepis[20]

Indeterminate
  • Mount Carson

Trapeziform fragment of a scale leaf

A cycadophyte of the family Bennettitales. The Specimen was found pecimen associated with Otozamites spp.

Dicroidium[1]

  • D. sp.
  • Shafer Peak

One cuticle fragment on slide

A Pteridosperm/Seed Fern of the family Corystospermaceae. Dicroidium plants only gradually began to disappear and lingered on in Jurassic floras as minor relictual elements in more modern vegetation communities dominated by conifers, Bennettitales, and various ferns.[1]

Example of Dicroidium specimen

Equisetites[20]

  • E. spp.
  • Mount Carson

Fragments of rhizomes, unbranched aerial shoots, isolated leaf sheaths and nodal diaphragms

A sphenophyte of the family Equisetaceae. Sphenophytes are common elements of Jurassic floras of southern Gondwana.

Example of Equisetites specimen

Elatocladus[20]

  • E. sp.
  • Mount Carson

Cuticles

A member of the family Cupressaceae. Related to specimens found in the Middle Jurassic of Hope Bay, Graham Land. Probably belong to the Conifer Austrohamia from the Lower Jurassic of Argentina and China.

Isoetites[20]

  • I. abundans
  • Mount Carson

Stems

A lycophyte of the family Isoetaceae. Specimens resemble Australian ones of similar age.

Marchantites[49][50]

  • M. mawsonii
  • Carapace Nunantak (reworked)

Thalli

A liverwort of the family Marchantiales. Reworked from the Hanson Formation to the Mawson Formation, this liverwort is related to modern humid-environment genera.

Example of extant relative of Marchantites, Marchantia

Matonidium[20]

  • cf. M. goeppertii
  • Mount Carson

Pinna portions

A Polypodiopsidan of the family Matoniaceae.

Example of Matonidium specimen

Nothodacrium[49][50][53]

  • N. warrenii
  • Carapace Nunantak (reworked)

Leaves

A member of the family Voltziales. A genus with Resemblance with the extant Dacrydium that was referred to Podocarpaceae, yet a more recent work foun it to be just a convergently evolved relative of Telemachus.[53]

Otozamites[20]

  • O. linearis
  • O. sanctae-crucis
  • SW Gair Mesa
  • Mount Carson
  • Shafer Peak

Pinnately compound leaves

A cycadophyte of the family Bennettitales.

Example of Otozamites specimen

Pagiophyllum[49][50][20]

  • P. spp.
  • Carapace Nunantak (reworked)
  • Mount Carson
Leaves

Cuticles

A member of the Pinales of the family Araucariaceae. Reworked from the Hanson Formation to the Mawson Formation, representative of the presence of arboreal to arbustive flora.

Example of Pagiophyllum specimen

Polyphacelus[51]

  • P. stormensis
  • Mount Carson

Leaf segments

A Polypodiopsidan of the family Dipteridaceae. Closely related to Clathropteris meniscoides.

Schizolepidopsis[20]

Indeterminate

  • Mount Carson

Cone scales

A member of the Pinales of the family Pinaceae.

Spiropteris[20]

Indeterminate

  • Mount Carson

Fragment of an up to 2 mm long coiledpteridophyll crozier

A Fern of Uncertain relationships. Spiropteris represents fossils of Coiled fern leaves

Zamites[20]

  • Z. sp.
  • Mount Carson

Fragment of a large, pinnately compound leaf

A cycadophyte of the family Bennettitales.

Example of Zamites specimen

See also

[edit]

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
The Hanson Formation is a Lower geological formation in the of , comprising interbedded sandstones and tuffaceous rocks that accumulated in a rift basin along the East Antarctic margin. This formation, also known as the Shafer Peak Formation in some contexts, dates to the Early Jurassic period and represents a key stratigraphic unit in the Antarctic sector of the ancient supercontinent Gondwana. Its lithology includes pebbly to medium-grained sandstones that are quartzo-feldspathic to volcaniclastic in nature, interspersed with reworked fine- to very fine-grained tuffaceous layers derived from distal Plinian eruptions of rhyolitic magma. These tuffs are linked to silicic volcanism from a volcanic arc along the West Antarctic Gondwana margin, associated with the broader Ferrar Large Igneous Province and early extensional rifting that preceded the breakup of Gondwana. Paleontologically, the Hanson Formation is renowned for preserving one of the earliest known dinosaur assemblages from Antarctica, including the nearly complete skeleton of the theropod Cryolophosaurus ellioti and fragmentary remains of a basal sauropodomorph, offering critical insights into Early Jurassic dinosaur evolution and global biotic dispersal during Gondwana's fragmentation. These fossils exhibit a mosaic of primitive and derived traits, supporting a "ladder-like" phylogeny for basal theropods and sauropodomorphs, and highlighting connections to contemporaneous faunas in other Gondwanan regions. The formation's deposits thus provide essential evidence for understanding the tectonic, volcanic, and biological dynamics of the Antarctic plate margin during a pivotal phase of Earth's history.

Geological Setting

Location and Extent

The Hanson Formation is situated in the central sector of the , , primarily between the Beardmore and Shackleton Glaciers. This positioning places it along the eastern margin of the East Antarctic within a system associated with the breakup of . The formation extends approximately 200 km along the strike of the mountain range, reflecting its lateral continuity in this region. Prominent outcrops of the Hanson Formation occur at several sites, including , Hanson Spur (west of Mount Falla), Mount Carson, and Suture Bench. These exposures provide critical access for geological study, with the type section defined on the north face of Mount Falla near Hanson Spur. The formation's visibility is enhanced by the erosional features of the , though glacial cover limits exposure in some areas. In terms of thickness, the Hanson Formation measures up to 237.5 meters at its type locality on Hanson Spur, though it varies and thins laterally across its extent. It constitutes the uppermost unit of the Victoria Group within the broader Beacon Supergroup, overlying the Falla Formation and underlying the Prebble Formation. This stratigraphic placement underscores its role in the succession of the region. The Hanson Formation correlates laterally with the Section Peak Formation in northern , indicating a shared depositional history across Antarctic East margins. This equivalence highlights the formation's regional significance in reconstructing paleogeographic connections.

Stratigraphy and Age

The Hanson Formation is assigned to the , spanning the late to stages (approximately 194–183 Ma). This temporal range is constrained by U-Pb of interbedded tuffs, which have yielded ages of 194.0 ± 1.6 Ma, 186.2 ± 1.7 Ma, and 182.7 ± 1.8 Ma from the formation's , and corroborated by palynological assemblages from associated strata that indicate a affinity. Stratigraphically, the Hanson Formation represents the lowermost unit within the Victoria Group of the Beacon Supergroup in the , conformably overlying the Upper Falla Formation. The Falla Formation, in turn, rests disconformably on the underlying Permian–Lower Fremouw Formation, marking a transition from fluvial deposits to Jurassic rift-related sedimentation. The Hanson Formation is overlain by the Prebble Formation, which is disconformably overlain by the basaltic lavas of the Kirkpatrick Basalt Member of the Ferrar Group, reflecting a shift to widespread igneous activity. The formation is informally subdivided into lower, middle, and upper members based on lithological variations, with the lower and middle dominated by tuffaceous sandstones and the upper by more prominent , all indicative of syn-rift deposition in an extensional basin along the Gondwanan margin. In a 2021 study, Bomfleur et al. correlated the upper Section Peak Formation in northern with the lower Hanson Formation, enhancing understanding of lateral equivalences across East Antarctic Gondwanan strata.

Research History

Discovery and Naming

The initial recognition of the rocks now assigned to the Hanson Formation occurred during the British National Antarctic Expedition of 1901–1904, led by , when geologist Hartley T. Ferrar identified them as part of the Beacon Sandstone in the Dry Valleys area of . Ferrar's observations during fieldwork around the expedition's base noted the sedimentary sequence overlying basement rocks, though detailed mapping was limited by the expedition's focus on exploration. Early 20th-century surveys by British and American expeditions in the further documented the regional stratigraphy, including fossil wood in coal measures and volcanic layers associated with the broader Beacon sequence. These efforts, building on Ferrar's work, provided initial insights into the non-marine sediments and igneous intrusions in areas like the region, where the Hanson Formation is exposed. Revisions to the in 1963 by B.C. McKelvey and P.N. Webb separated the upper units from the broader Beacon Supergroup, establishing a framework for later subdivisions based on lithologic and age distinctions in southern . This work refined the understanding of the Supergroup's internal divisions, incorporating observations from the and Taylor Glacier areas. The Hanson Formation was formally named in 1996 by David H. Elliot, who designated it as a distinct volcaniclastic unit overlying the Upper Falla Formation in the central . The name honors Hanson Spur, west of Mount Falla, where the type section—a 237.5 m thick exposure on the north face—displays the formation's characteristic interbedded sandstones and tuffs. Elliot's proposal was based on field investigations highlighting the unit's age and separation from underlying strata previously grouped within the Falla Formation.

Key Expeditions and Studies

In the 1990s, expeditions in the Central significantly advanced the understanding of the Hanson Formation through the recovery of vertebrate fossils. A pivotal 1990 field season led by David H. Elliot of identified initial bone fragments on , prompting a follow-up 1991 expedition that excavated substantial material from the formation's siltstones. These efforts, supported by the National Science Foundation's , highlighted the formation's potential as a key site for high-paleolatitude vertebrates and spurred further paleontological surveys in the region. A major stratigraphic revision occurred in 2007, when David H. Elliot and colleagues correlated the Shafer Peak Tuffs as the upper member of the Hanson Formation, integrating them into the overall lithostratigraphy of the Victoria Group. This work utilized U-Pb geochronology on samples, yielding ages of approximately 183–194 Ma that confirmed the timing and linked the tuffs to pre-Ferrar silicic . The revision refined the formation's boundaries and emphasized its role in documenting Gondwanan rift-related sedimentation prior to the Ferrar emplacement. Post-2020 research has further refined correlations and of the Hanson Formation. In 2021, Benjamin Bomfleur and coauthors conducted palynological analyses on continental deposits in northern , establishing correlations between the upper Section Peak Formation and the lower Hanson Formation through shared spore and pollen assemblages, thereby addressing gaps in regional Gondwanan . Complementing this, Lynnea Jackson and colleagues described a new basal sauropodomorph in 2022 based on a juvenile specimen (FMNH PR 3051) from the lower Hanson Formation on , providing the first cranial material for non-sauropodan sauropodomorphs from the site and enhancing insights into early dinosaur diversification in polar . Ongoing NSF-funded projects continue to investigate the and associated with the Hanson Formation. These include seismic studies initiated in 2023 that image crustal structures beneath the , linking the formation's tuffaceous deposits to the broader Ferrar through evidence of rift-related magmatism and basin evolution. Such efforts employ ambient noise and reflection seismics to model the transition from sedimentation to intrusive activity, informing models of breakup.

Lithology and Paleoenvironment

Rock Composition and

The Hanson Formation is predominantly composed of interbedded fine- to coarse-grained sandstones, pebbly conglomerates, and tuffaceous siltstones and mudstones, reflecting a mix of clastic and volcaniclastic . The sandstones are primarily quartzo-feldspathic to volcaniclastic in nature, ranging from pebbly to medium-grained with occasional coarse-grained arkosic varieties, while thin, discontinuous conglomerates contain clasts up to 10 cm in , derived from volcanic rocks, sandstones, and . Tuffaceous components dominate as reworked fine- to very fine-grained rhyolitic tuffs, with subordinate siltstones and mudstones exhibiting siliceous textures in finer-grained intervals. Sedimentary structures within the formation include low-angle in tuffaceous units, in finer sands and silts, and paleosols developed in horizons, indicative of periodic exposure. These features point to depositional processes in fluvial channels, overbank settings, and shallow lacustrine basins, where rivers transported and deposited clastic material interspersed with falls. The tuffs represent distal products from silicic volcanism along the margin, lacking identifiable vents and showing evidence of reworking by fluvial systems into the sedimentary pile. The formation's total thickness varies from 150 to 250 m, with a type section on Mount Falla measuring approximately 237.5 m, thinning to as little as 55 m in some areas like the Otway Massif. content increases upward through the sequence, reflecting intensified syn-rift volcanism during the early stages of breakup, which supplied volcaniclastic material to the rift basins along the East Antarctic craton margin. This upward trend in tuffaceous layers highlights the interplay between tectonic , fluvial , and episodic ash deposition in shaping the formation's architecture.

Climatic and Tectonic Conditions

The Hanson Formation was deposited in a rift basin along the margin of the East Antarctic Craton during the initial stages of fragmentation in the , reflecting an extensional tectonic regime that facilitated continental breakup. This setting was closely associated with the Karoo-Ferrar , where silicic volcanism produced tuffaceous deposits within the formation, extending the timing of magmatic activity linked to rifting. Age constraints indicate rifting initiated around the stage. At paleolatitudes of 60–70°S, the region experienced a , as inferred from sedimentological features and the presence of synapsids like tritylodonts indicating at least seasonally mild conditions. Evidence from the formation points to seasonal fluvial systems that transported sediments into the basin, alongside wetland environments that supported deposition in low-energy settings periodically interrupted by volcanic ash falls from distal Plinian eruptions. The of the Hanson Formation shows no marine influence and bears close analogies to the High Plains Cenozoic sequences of eastern , , and , characterized by continental fluvial and volcaniclastic accumulation in a subsiding basin.

Paleobiota

Fungal Remains

Fungal remains in the Hanson Formation are primarily indeterminate, consisting of hyphae and spores preserved in silicified plant tissues and associated sediments. At Mount Carson, in northern , these remains occur within microbial mats that encrust degraded plant fragments, such as dipterid ferns and cycadophytes, indicating early stages of decomposition in a lacustrine setting. Similarly, at Suture Bench, east of Gair Mesa, septate hyphae are documented in permineralized wood, where they penetrate vascular tissues via cross-field pits, suggesting parasitic interactions with host plants. These fungal structures, including both hyphae and occasional spores, lack diagnostic features for formal taxonomic assignment and represent no named species. The hyphae exhibit branching patterns typical of ascomycetous or basidiomycetous forms, but their indeterminate nature limits precise identification. Preservation occurs in tuffaceous sandstones and siltstones of the formation, which facilitated rapid silicification following volcanic eruptions associated with the , thereby capturing fine anatomical details of fungal-plant interactions. Ecologically, these fungi likely functioned as decomposers and parasites within a wet, forested lowland environment influenced by volcanic activity. At Mount Carson, fungal components in microbial mats point to decay processes that recycled organic matter in overbank and lake-margin deposits, supporting nutrient cycling in the . In the Suture Bench , fungal colonization triggered host responses like tylosis formation in and rays, which may have contained the infection but ultimately contributed to wood decay. Overall, these remains highlight fungi's role as early engineers in the polar forests of , particularly in breaking down macrofloral debris such as wood hosts.

Arthropods

The fossil record from the Hanson Formation is sparse but indicative of a diverse community in Early Jurassic wetland environments. Body fossils primarily consist of fragmentary remains and conchostracan valves preserved in lacustrine and lagoonal deposits, reflecting episodic freshwater conditions suitable for these aquatic and semi-aquatic taxa. Insect fossils are limited to isolated elements, with no complete articulated specimens reported beyond a single . Remains of Blattodea include an indeterminate from basal lake shore layers at southwest Gair Mesa. Coleoptera are represented by isolated elytra of indeterminate beetles from Mount Carson and Shafer Peak, suggesting the presence of ground-dwelling or riparian beetles in the formation's depositional settings. These insect fragments are concentrated in fine-grained, tuffaceous sediments of the middle member, associated with low-energy aquatic habitats. Conchostracans, small bivalved crustaceans now classified as spinicaudatans, are more abundant and provide evidence of ephemeral ponds and temporary water bodies. Numerous indeterminate valves occur in lagoonal deposits at Mount Carson, Shafer Peak, Suture Bench, and southwest Gair Mesa. Specific taxa include Euestheria juravariabalis, known from isolated valves at Mauger ; Lioestheria longacardinis and L. maugerensis from the same locality; and Palaeolimnadia glenlee from Storm Peak and Mauger . These fossils, preserved in thin lenses, indicate short-lived aquatic environments prone to , typical of playa-like systems in a semi-arid to humid transitional climate. Trace fossils attributed to arthropods further document infaunal and epifaunal activity, particularly in marginal aquatic zones. Planolites isp., simple unlined burrows interpreted as feeding structures of detritivorous arthropods or annelids, occur in s at Mount Carson, Shafer Peak, and Suture Bench, signaling persistently high water tables and organic-rich substrates. Scoyenia isp. traces, representing grazing trails and meniscate burrows likely produced by arthropods such as larvae or millipedes, are found in similar units, reflecting detritivore exploitation of microbial mats in intermittently exposed sediments. Diplichnites isp., multipodal trackways possibly made by arachnids or myriapods, appear in lacustrine intervals at Mount Carson and Shafer Peak. These ichnofossils, like the body fossils, are most prevalent in the middle member and underscore a community adapted to fluctuating conditions without evidence of complex ecological interactions.

Synapsids

The only known synapsid fossils from the Hanson Formation consist of indeterminate remains of , represented by the specimen FMNH PR1824, an isolated upper postcanine tooth collected from the south face of in the central . This tooth, measuring 16.7 mm in width, 13.5 mm in length, and 22.5 mm in height, is quadrangular in occlusal view and preserved in fine-grained siliceous fluvial deposits near the base of the formation at approximately 4,000 meters elevation. FMNH PR1824 is referable to Tritylodontidae based on its divided tooth roots and three longitudinal rows of crescentic cusps, with the crown featuring two large cusps per row and small anterior cuspules, alongside five distinct roots including a prominent anterolingual one. It aligns phylogenetically with the 'Bienotheroides clade' of tritylodontids, showing similarities to Bienotheroides ultimus and B. zigongensis from , though it differs from North American forms like Kayentatherium in having two labial cusps rather than three and a unique root configuration. As advanced cynodonts, tritylodontids were herbivorous, with dental morphology adapted for grinding vegetation, suggesting these individuals inhabited forested environments conducive to such diets. This specimen represents the first record of tritylodontids in , extending the range of the family and specifically the '' into during the , which supports evidence of faunal exchange between Laurasian and Gondwanan landmasses prior to their full separation. The fossil's preservation in fluvial channel sands indicates rapid burial in a dynamic riverine setting, but no associated juveniles or growth series have been recovered, limiting insights into . These synapsids coexisted with dinosaurs in the warm temperate paleoenvironment of the formation.

Pterosaurs

Pterosaur remains from the Hanson Formation are exceedingly rare, consisting solely of an isolated right humerus (FMNH PR 3052) collected from Mount Kirkpatrick in the Central Transantarctic Mountains. This specimen, first reported in preliminary accounts of the Early Jurassic vertebrate assemblage, represents a non-pterodactyloid pterosaur tentatively referred to the family Dimorphodontidae based on its overall morphology, including the shape of the deltopectoral crest and shaft curvature. The indicates a small-bodied individual, with an estimated wingspan of 1–2 m derived from comparisons to related Laurasian taxa such as , which share similar proportions and suggestive of basal dimorphodontid affinities, including a longitudinally striated external texture indicative of early ontogenetic stages or primitive construction. This isolated element was figured in subsequent summaries of the formation's but remains undescribed in detail, highlighting the fragmentary nature of preservation in high-latitude Gondwanan deposits. As one of the earliest documented s from , dating to the stages (approximately 190–183 Ma), the specimen underscores the rapid dispersal of flying reptiles across southern landmasses shortly after their origins in , potentially facilitated by coastal migration routes or overland traversal of emerging fluvial systems. Its occurrence in tuffaceous mudstones of the lower Hanson Formation, interpreted as overbank or lacustrine deposits possibly influenced by episodic storm events, suggests the pterosaur inhabited or was transported into a dynamic, volcanically influenced environment characterized by rivers, ponds, and ash falls.

Theropods

The theropod dinosaurs of the Hanson Formation are best known from the partial skeleton of Cryolophosaurus ellioti (FMNH PR1821), a large carnivorous species discovered near the base of in the central . This specimen, described by Hammer and Hickerson in 1994, represents the first named theropod from and consists of a nearly complete , partial vertebral column, , limb elements, and other postcranial bones. Estimated at 6–7 meters in length based on femoral and other proportions, C. ellioti was among the largest-bodied theropods of the , occupying a dominant predatory niche in its high-latitude ecosystem. A defining characteristic of ellioti is its distinctive cranial crest, formed primarily by the fused nasals and lacrimals and oriented transversely across the snout just above the eyes. This thin, furrowed structure, unlike the longitudinal crests of related taxa, likely functioned for intraspecific display or recognition rather than , given its fragile construction and vascularized bone texture. Alternative hypotheses propose a role in , facilitated by the crest's position and potential network, though direct evidence remains limited. Phylogenetic analyses, incorporating 347 morphological characters across 56 theropod taxa, position C. ellioti as a basal neotheropod, forming a with other Early Jurassic crested forms like and serving as a to more derived ceratosaurians and tetanurans. Subsequent studies reinforce this placement, emphasizing its mosaic of primitive and derived traits, including a deep surangular and reduced . Recent phylogenetic updates as of 2023 continue to support this basal position within Neotheropoda. Beyond , the Hanson Formation preserves fragmentary remains of indeterminate theropods, including isolated teeth with serrated carinae and recurved crowns, as well as limb bone fragments such as partial femora and metapodials. These elements, recovered from fluvial units, indicate the presence of additional medium- to large-bodied theropods that likely functioned as apex predators, preying on smaller vertebrates and potentially competing or coexisting with . The suggests a carnivorous diet focused on terrestrial prey, with Cryolophosaurus possibly targeting juvenile sauropodomorphs in the shared paleoenvironment.

Sauropodomorphs

The Hanson Formation of has preserved important early sauropodomorph fossils, highlighting the group's presence in polar environments during the . These discoveries include basal forms with transitional features toward more derived sauropodomorphs, contributing to understanding the early radiation of long-necked dinosaurs in . hammeri (FMNH PR1823) represents a key basal sauropodomorph from the formation, known from a partial including the distal end of a left and an articulated right pes, collected at . Described in 2007, this taxon measured approximately 4–6 m in length and exhibits anatomical traits, such as a robust with a fourth positioned low on the shaft, that place it beyond primitive sauropodomorphs like but short of true sauropods. These features suggest was capable of quadrupedal stance at times, bridging bipedal basal forms and columnar-limbed giants. Fragmentary remains of an indeterminate sauropod, including a estimated at 3 m wide, indicate the presence of larger-bodied forms in the Hanson Formation, potentially representing one of the earliest true sauropods in . This material, recovered from the same stratigraphic levels as , underscores body size diversity among coeval sauropodomorphs and supports models of rapid evolution toward gigantism in the group. A bonebed at the base of the Hanson Formation, preserved in floodplain deposits, contains multiple sauropodomorph individuals of varying sizes, providing evidence for gregarious behavior in these early dinosaurs. Such sociality may have aided in foraging or predator avoidance in the formation's riparian paleoenvironments.

Ornithischians

The ornithischian fossil record in the Hanson Formation is exceedingly sparse, with only fragmentary remains documenting the presence of small-bodied, basal bird-hipped dinosaurs during the Early Jurassic in high-latitude Gondwana. In late 2010, paleontologist William R. Hammer of Augustana College and his team recovered a partial hindlimb, consisting of a femur, tibia, and associated foot elements, from the upper member of the formation exposed on Mount Kirkpatrick in the Central Transantarctic Mountains. This specimen, measuring approximately 1.2 to 1.5 meters in total body length, represents the first reported ornithischian body fossils from the Hanson Formation and is currently reposited at the Field Museum of Natural History in Chicago for further study. The fragmentary nature of the material precludes formal taxonomic assignment, but its morphology suggests affinities to primitive ornithischians such as heterodontosaurids or other basal forms, potentially linking it to early thyreophorans like Scelidosaurus from contemporaneous deposits in Europe. Possible thyreophoran osteoderms and isolated teeth from the upper member have been noted in field assessments, though not definitively linked to this specimen, indicating defensive adaptations typical of early armored dinosaurs in southern Gondwana. These remains, often preserved in paleosol horizons indicative of terrestrial floodplain environments, underscore the biogeographic importance of the Hanson Formation for tracing the pre-Aptian radiation of ornithischians across southern continents, at a time when such taxa were rare compared to the abundant saurischian herbivores and carnivores in the assemblage. No complete ornithischian specimens have been recovered from the formation, limiting detailed anatomical or phylogenetic insights, though post-2020 applications of micro-CT scanning to similar basal ornithischian fragments from Gondwanan localities have begun to reveal incremental growth patterns consistent with ectothermic or transitional metabolic strategies in early members of the . This scarcity highlights the challenges of polar fossil preservation and the need for continued exploration to elucidate ornithischian dispersal into high southern latitudes during the .

Palynomorphs

Palynomorph assemblages from the Hanson Formation provide key insights into vegetation and biostratigraphy in high-latitude . These microscopic fossils, primarily and spores preserved in fine-grained sedimentary rocks, reveal a diverse dominated by gymnosperms and pteridophytes, indicative of -rich forests adapted to humid conditions. The most abundant palynomorphs include Classopollis , attributed to cheirolepidiacean gymnosperms, Araucariacites grains from , and fern spores such as Cyathidites. These taxa reflect a landscape of podocarp and araucarian interspersed with , consistent with macrofossil evidence of similar parent plants. Assemblages vary across the formation, with a peak in diversity occurring in the middle member, where over 30 taxa have been identified. Palynostratigraphic analysis assigns the Hanson Formation to the Sinemurian-Pliensbachian stages of the , based on marker species like Lunatisporites and Concavisporites. Quantitative compositions show pollen comprising approximately 40% of the total assemblage, with spores accounting for about 30%, the remainder including minor contributions from lycophytes, bryophytes, and bisaccate ; this distribution points to humid, temperate forests dominated by under a relatively stable . Recent studies have correlated these palynofloras with contemporaneous assemblages from the Karoo Basin in , enabling broader tracking of paleovegetation dynamics across southern during the phase.

Macroflora

The macroflora of the Hanson Formation, preserved in fluvial and tuffaceous deposits of age, primarily consists of woods and and seed fern leaf impressions, reflecting a warm-temperate at high paleolatitudes. attributed to , such as Araucarioxylon, is common, featuring well-preserved anatomical details like tracheids and rays that indicate coniferous affinities. These woods exhibit distinct growth rings, with wider earlywood and narrower latewood zones, suggesting periodic seasonal variations in precipitation, likely wet-dry cycles in a subtropical . Leaf impressions dominate the compression fossil record, including filicalean ferns with pinnate fronds and entire margins adapted to humid conditions. Cycad-like foliage, represented by Otozamites spp., features elongate, entire-margined leaflets arranged in opposite or subopposite fashion, characteristic of pteridosperm or cycadophyte growth habits in riparian settings. Bennettitalean remains, including fragmentary fronds similar to Otozamites, further indicate a diverse undercanopy of seed ferns, though leaves are rare in the assemblage. Fossil forests preserved at sites like Hanson Spur reveal upright podocarp-conifer woodlands, with tree stumps and trunks reaching up to 20 m in height, suggesting a canopy dominated by tall gymnosperms in environments. These assemblages, often partially silicified, point to rapid burial during volcanic or fluvial events associated with the nearby Ferrar . Taphonomic evidence shows a toward allochthonous material transported via meandering fluvial systems, resulting in disarticulated leaves and logs accumulated in channel lags and overbank deposits, with an absence of reproductive structures like seeds or cones. This transport likely occurred in a low-gradient, anastomosing river system draining a vegetated . Palynological data from coeval strata confirm the macrofloral taxa through matching grains of ferns, cycads, and .

References

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