Triassic land vertebrate faunachrons

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Land vertebrate faunachrons (LVFs) are

synapsids and faunal assemblage zones estimated to correspond to the Early Triassic. These are followed by the Perovkan and Berdyankian, based on temnospondyl amphibians and Russian assemblages estimated to be from the Middle Triassic. The youngest four Triassic LVFs, the Otischalkian, Adamanian, Revueltian, and Apachean, are based on aetosaur and phytosaur reptiles common in the Late Triassic of the southwestern United States.[1][3][4]

The LVF system, though widely used, is also a controversial application of

index fossils. Limited occurrences, inaccurate age estimates, overlapping LVF faunas, or taxonomic disagreement may jeopardize global correlations between Triassic tetrapods. This could render some LVFs as misleading assessments of Triassic faunal change through time.[5][6][7][8] Regardless, Late Triassic phytosaurs are considered to have strong biostratigraphic utility even among detractors of Lucas's system.[9]

Lucas's LVFs

Tetrapod biostratigraphy has been used for the Triassic of

Land Mammal Age (LMA) system already in use for Cenozoic
faunal assemblages.

Triassic tetrapod biozones, under the term "land vertebrate faunachrons" (LVFs) were formalized on a global level by Lucas in 1998. They were diagnosed by a primary

index fossil (a particular genus of widespread time-constrained tetrapod) and characterized by a faunal type assemblage (distinguishing collection of taxa) from a fossiliferous geological formation. Together, the defining index fossil and assemblage could be used to correlate fossil assemblages worldwide.[1] Updates to this system have been published continuously for Triassic LVFs, which remain a heavily-discussed topic in the study of Triassic chronology.[13][3][14][4] Lucas has also defined LVFs for the Permian,[2][15][16] Jurassic,[17] and Carboniferous,[18]
though these are not as widely used as his Triassic LVFs.

Later authors characterized Lucas's LVFs as "interval eubiochrons". This means that they correspond to a segment of time (and strata) between two paleobiological events: the first appearance datum (FAD) of one index taxon and the FAD of another.[9] A first appearance datum is a point in the geological record with the earliest known fossil of a given animal, which can estimate when that animal speciates or evolves into existence. As an example, the Lootsbergian LVF is defined as the period of time between the FAD (estimated speciation) of Lystrosaurus and the FAD (estimated speciation) of Cynognathus. Some taxa which are index fossils for one stage may persist into a later stage.[1]

List of Triassic LVFs

LVFs of the Triassic Period from youngest to oldest:

LVF name Namesake Primary index fossil Other index fossils Proposed age estimate
(but see below) 		Type assemblage Other correlated assemblages
Apachean Apache Canyon, New Mexico, USA[12]

Redondasaurus
 Redondasuchus, Riojasaurus late Norian to Rhaetian Redonda Formation, New Mexico, USA
Lower Elliot Formation? (South Africa), upper Mercia Mudstone Group? (UK), lower Penarth Group? (UK), Rhaetian fissure fills
? (UK)
Revueltian Revuelto Creek, New Mexico, USA[12]

Typothorax coccinarum[3]
Pseudopalatus-grade phytosaurs, Eudimorphodon[3]
 early to middle Norian

(but see below)

Bull Canyon Formation
, New Mexico, USA
Lower Elliot Formation? (South Africa)[4]
Adamanian Adamana, Arizona, USA[12]

Rutiodon-grade phytosaurs (including Leptosuchus and Smilosuchus)
 Stagonolepis, Spinosuchus,[3] Colognathus,[3] Tecovasaurus,[3] Crosbysaurus[3] late Carnian

(but see below)

Blue Mesa Member, Chinle Formation, Arizona, USA
Kieselsandstein (Germany),[3] DeGeerdalen Formation (Svalbard),[4] Ischigualasto Formation (Argentina), upper Santa Maria Formation (Brazil), Caturrita Formation (Brazil),[3] upper Maleri Formation (India), Isalo II (Madagascar)[3]
Otischalkian Otis Chalk, Texas, USA[12]

Paleorhinus / Parasuchus
 Metoposaurus, Placerias,[3] Hyperodapedon,[3] Doswellia, Angistorhinus, Longosuchus middle Carnian Colorado City Formation, Texas, USA Popo Agie Formation (Wyoming, USA), Salitral Formation (New Mexico, USA), "Sanfordian" strata of the Newark Supergroup (eastern USA and Canada), Stuttgart Formation (Germany), Timezgadiouine Formation (Irohalene Member, Morocco), lower Maleri Formation (India), Tiki Formation (India),[4] Madygen Formation? (Kyrgyzstan)
Berdyankian Berdyanka River, Russia

Mastodonsaurus giganteus[3]
 Massetognathus, Dinodontosaurus, Stahleckeria late Anisian to early Carnian[4]
Bukobay Formation
, Russia
Lower Keuper (Germany), Chañares Formation (Argentina), lower Santa Maria Formation (Brazil), upper Omingonde Formation (Namibia)[4]
Perovkan Perovka, Russia

Eocyclotosaurus[3]
Kannemeyeria cristarhynchus",[3] Arizonasaurus[3]
 Anisian Donguz Formation, Russia
Manda Beds
(Tanzania)
Nonesian Nonesi's Nek Pass, South Africa

Cynognathus
Kannemeyeria simocephalus, Erythrosuchus[3]
 Olenekian Cynognathus Assemblage Zone (Subzones A-B), South Africa
Kingori Sandstone (Tanzania), upper Fremouw Formation
(Antarctica)
Lootsbergian Lootsberg Pass, South Africa

Lystrosaurus
 Wetlugasaurus, Tupilakosaurus, Luzocephalus, Lydekkerina, Scaloposaurus, Thrinaxodon, Procolophon, Prolacerta, Proterosuchus latest
Changxingian) to Induan
 Lystrosaurus Assemblage Zone, South Africa upper Guodikeng Formation (China), lower Jiucaiyuan Formation (China), Heshanggou Formation (China), lower Fremouw Formation (Antarctica), Panchet Formation (India), Wordie Creek Formation (Greenland), Vokhmian Gorizont (Russia),[3] Sludkian Gorizont (Russia),[3] Ustmylian Gorizont (Russia),[3] Sanga do Cabral Formation (Brazil),[3] Rewan Formation (Australia),[3] Arcadia Formation (Australia)[3]

Criticism

Several paleontologists have independently questioned the validity of Lucas’s system, criticizing its inconsistent and often contradictory approach to taxonomy and faunal correlations.[5][6][7][8]

Endemic index taxa

Many index taxa are very rare or endemic to a single continent, and have no relevance to a global biostratigraphy system. These include

dicynodonts are conjectural and based on undiagnostic European fragments.[5][7]

Imprecise or inaccurate time scales

Index taxa for a given LVF often range into the succeeding LVF, blurring the distinction between the two time periods. Angistorhinus, Hyperodapedon, Paleorhinus/Parasuchus (all Otischalkian index taxa) range into the Adamanian, fossils referred to Rutiodon (an Adamanian index taxon) range into the Revueltian, and Metoposaurus can be found throughout the Otischalkian, Apachian, and Revueltian LVFs.[5][6][7][21]

Lucas's approach to correlating LVFs with global marine stages has been met with criticism. The Triassic timescale is under constant revision from a series of age dating methods, including

conchostracan biozones can help correlate terrestrial strata to an extent. One complication is that Lucas's view of the Late Triassic time scale contradicts the consensus established by other biostratigraphers. Most paleontologists estimate that the three stages of the Late Triassic (Carnian, Norian, and Revueltian) are strongly unequal in size, with the Norian far longer than the Carnian. Under this consensus "long-Norian" hypothesis, the Carnian-Norian boundary is close to 228 Ma. Lucas, on the other hand, prefers a "short-Norian" perspective, with a lengthier Carnian stage and a Carnian-Norian boundary at around 220 Ma.[8]

For example, Lucas has maintained that the lower part of the Chinle Formation (the Blue Mesa Member and equivalent units) is Carnian (>220 Ma) in age. This was justified by the assumption that fossils of Stagonolepis, a European aetosaur, can be found in North and South America, allowing correlation between these regions. However, this proposed widespread occurrence of Stagonolepis is a debatable, as many species assigned to the genus may not be closely related (see below).[1][3][6][21]

According to the "short-Norian" interpretation, these lower Chinle Formation, and other strata of the Adamanian LVF, would be firmly pre-Norian in age, suggesting that any taxonomic change between the Adamanian and Revueltian represents a Carnian-Norian extinction event. However, the consensus "long-Norian" interpretation firmly places Adamanian strata of North America into the Norian stage (<228 Ma). The Norian age of the lower Chinle Formation has been independently confirmed by

U-Pb dating and magnetostratigraphic correlations to global time scales.[8][27][28] Conversely, other "Adamanian" strata, such as fossiliferous layers in the lower Ischigualasto Formation of Argentina, can be assigned to the late Carnian (~231 Ma).[6][29] This supports the conclusion that LVFs such as the Adamanian are fraught with uncertain time estimates brought on by weak correlations on a global scale.[6][8]

Some authors have elected to ignore LVFs in favor of older and more localized biostratigraphic units. Named tetrapod assemblages zones (AZs) were well-established for the Triassic of Gondwana prior to the LVF, and recent updates have helped to constrain these units with greater clarity and agreement than global correlations. In Argentina,

cynodont Exaeretodon, as well as the aetosaur Aetosauroides and herrerasaurid dinosaurs.[6]

Taxonomic uncertainty and dubious correlations

Mastodonsaurus, a purported index fossil of the Berdyankian LVF

Some correlations are based on connections between fragmentary or poorly-constrained taxa rather than direct correlations between type assemblages or LVF-defining index taxa. For example, the Ermaying Formation of China is correlated with the Moenkopi Formation of the United States via a tenuous (and likely unjustifiable) comparison between proposed erythrosuchid fossils. The primary index fossil of the Perovkan LVF, Eocyclotosaurus, is absent from China.[5][7]

One particularly contradictory index fossil is Mastodonsaurus, the defining index fossil of the Berdyankian LVF. Fossils referable to this genus can be found across Ladinian-age Europe, but the proposed Russian species (M. torvus) may be unrelated to the endemic German type species (M. giganteus). Moreover, if one approaches Mastodonsaurus from a broader taxonomic perspective (as expected if M. torvus is included), they must also incorporate Anisian and Carnian material referred to the genus, including the small species “Heptasaurus” cappelensis. This precludes any reason to use Mastodonsaurus as a time-constrained index taxon.[5][7]

Some LVFs are based on evolutionary grades as index taxa. This ignores the potential for high diversity and long temporal ranges within a given grade, and may lead to arbitrary and subjective inclusion or exclusion of descendant taxa. “Stagonolepis”, in its broadest form, is a wastebasket taxon of basal aetosaurs ranging through the Otischalkian and Apachean. Lucas’s usage of Stagonolepis lumps in many genera separated by other authors, such as Aetosauroides and Calyptosuchus.[6][7] A similar situation occurs in Paleorhinus/Parasuchus, which has historically been used as a persistent grade of early phytosaurs. On the other hand, the characteristic phytosaur (Redondasaurus) and aetosaur (Redondasaurus) genera of the Apachean LVF are very similar to, and perhaps synonymous with, index taxa of the underlying Revueltian LVF: “Pseudopalatus” (Machaeroprosopus) and Typothorax, respectively.[5][7]

Martz & Parker (2017) revision

Although the utility of a global LVF system is questionable, LVF-derived biostratigraphy may be useful in limited circumstances. Phytosaurs in particular have played a large role in the tetrapod biostratigraphy of the Chinle and Dockum Group of the southwest United States. A revision of the LVF system in this narrow context was undertaken by Jeff Martz and Bill Parker (2017), retaining several names and concepts previously used by Lucas and colleagues.[9]

Martz and Parker argued that the term "faunachron" was misleading and redundant, as each "faunachron" is bound by a single taxon rather than an assemblage (fauna) of multiple taxa. They preferred using a specific type of interval biozone known as a teilzone, referring to a local interval of strata equivalent to an interval of time.[9][30] The base of each teilzone was marked by the Lowest known Occurrence (LOk) of a particular category of phytosaur, i.e. the oldest layer where fossils of that category are found in the study area. LOks are local points in time and stratigraphy, disregarding occurrences in other regions or the estimated time of speciation. For the Otischalkian, Adamanian, and Revueltian, the top of each teilzone is marked by the LOk of a more exclusive subgroup of phytosaurs. The top of the Apachean is marked by the LOk of Protosuchus, an Early Jurassic crocodylomorph, as with Lucas's system.[9]

"Faunachrons" could also be defined beyond the constraints of teilzones; other biozonation categories include holochronozones (a stratigraphic interval, involving multiple study areas) and holochrons (an estimated time interval, involving the time of speciation or immigration into the region). Each phytosaur-based "faunachron" could be considered a teilzone (in local biostratigraphy), an estimated holochronozone (in regional chronostratigraphy), or an estimated holochron (in regional biochronology).[9]

One complication in defining biozones based on phytosaurs is instability in phytosaur systematics. Many proposed phytosaur taxa are dubious, paraphyletic (such as Leptosuchus and Machaeroprosopus) or have unclear relationships to each other. Nevertheless, a series of nested clades is apparent in most recent overviews. Rather than relying on a single index taxon per biozone, Martz and Parker allowed multiple representatives per a given stage of phytosaur evolution. These representatives were chosen based on their occurrence in the southwest United States, commonness, and relatively stable phylogenetic position despite paraphyly in some circumstances.[9]

Name Base-defining event Representative phytosaurs Estimated age Included Chinle units Included Dockum units
Apachean LOk of "Redondasaurus" "Redondasaurus" (subgenus of Machaeroprosopus?) Rhaetian (207-202 Ma)
  • Rock Point Member
  • Church Rock Member
  • "siltstone member”
  • Owl Rock Member
    (in part)
Revueltian LOk of
Pseudopalatinae (= Mystriosuchini
)
sensu lato
) 		middle to late Norian (Alaunian to
Sevatian
, 215-207 Ma)
Adamanian LOk of Leptosuchomorpha Smilosuchus, Leptosuchus, "Phytosaurus" doughtyi early to middle Norian (Lacian to early
Alaunian
, 224-215 Ma)
Otischalkian LOk of Phytosauria Wannia, Parasuchus (Paleorhinus) bransoni earliest
Lacian
, 227-224 Ma)

Adamanian-Revueltian turnover

Although most LVFs or equivalent concepts are not marked by major biotic changes, one exception is apparent in the southwest United States. The boundary between the Adamanian and Revueltian zones is marked by a faunal turnover, an event where several tetrapod species quickly disappear from the fossil record as others appear for the first time. At

pedogenic carbonate nodules may also support increasing aridity.[21][31]

The cause and relevance of this turnover is debatable, as it may indicate only a small localized extinction. The

K-Pg Mass Extinction at 66 Ma), is dated to around 215.4 Ma.[32][33] While certainly large enough to momentarily devastate areas near the impact point in Quebec, broader environmental effects of the Manicouagan impact are mostly conjectural.[8] Besides the Adamanian-Revueltian turnover, the impact has also been linked to a minor marine extinction in eastern Panthalassa.[34]

Alternatively, the Adamanian-Revueltian turnover may be a consequence of the gradual aridification of western Pangea as it drifted north into arid latitudes.[31] Comparative estimates of extinction rates and occurrences find little support for a synchronized Adamanian-Revueltian turnover, and instead support a model where extinctions are stretched out over several million years. For most species, extinction probabilities are "decoupled" in time from other species, as well as geological or climatological drivers. The only plausible correlation is between the Manicouagan Impact and palynomorph turnover, and even then the probability of synchronicity is only about 34%.[35]

References

  1. ^
    ISSN 0031-0182
    .
  2. ^ a b Lucas, Spencer G. (2005). "Permian Tetrapod Faunachrons". New Mexico Museum of Natural History and Science Bulletin. 30: 197–201.
  3. ^
    S2CID 128911449
    .
  4. ^
    ISBN 978-3-319-68009-5
    , retrieved 2020-05-31
  5. ^
    S2CID 129914103
    .
  6. ^
    ISSN 0895-9811
    .
  7. ^
    S2CID 86502146
    .
  8. ^ a b c d e f g Irmis, Randall B.; Martz, Jeffrey W.; Parker, William G.; Nesbitt, Sterling J. (March 2010). "Re-evaluating the correlation between Late Triassic terrestrial vertebrate biostratigraphy and the GSSP-defined marine stages" (PDF). Albertiana. 38: 40–53.
  9. ^
    ISBN 978-0-12-803243-5
    , retrieved 2022-08-28
  10. ^ Lucas, Spencer G. (1993). "Vertebrate biochronology of the Triassic of China". New Mexico Museum of Natural History & Science Bulletin. 3: 301–306.
  11. ^ Huber, Phillip; Lucas, Spencer G.; Hunt, Adrian P. (1993). "Vertebrate biochronology of the Newark Supergroup Triassic, eastern North America". New Mexico Museum of Natural History & Science Bulletin. 3: 179–186.
  12. ^ a b c d e Lucas, Spencer G.; Hunt, Adrian P. (1993). "Tetrapod biochronology of the Chinle Group (Upper Triassic), western United States". New Mexico Museum of Natural History & Science Bulletin. 3: 327–329.
  13. ^ Lucas, S.G.; Hunt, A.P.; Heckert, A.B.; Spielmann, J.A. (2007). "Global Triassic tetrapod biostratigraphy and biochronology: 2007 status" (PDF). In Lucas, S.G.; Spielmann, J.A. (eds.). The Global Triassic. New Mexico Museum of Natural History and Science Bulletin. Vol. 41. pp. 229–240. Archived from the original (PDF) on 2011-09-27. Retrieved 2010-07-17.
  14. ISBN 978-3-319-04364-7
    .
  15. S2CID 129613959
    .
  16. S2CID 134768451
    .
  17. ^ Lucas, S. (2008). "Global Jurassic tetrapod biochronology". Volumina Jurassica. 6 (1): 99–108.
  18. S2CID 235528136
    .
  19. doi:10.14241/asgp.2015.024
    .
  20. S2CID 91926999
    .
  21. ^
    S2CID 140536630
    .
  22. doi:10.3389/feart.2020.00196
    .
  23. PMID 17919771
    .
  24. ^ Retallack, G. J.;
    doi:10.1130/0016-7606(1996)108<0195:GCGBPT>2.3.CO;2
    . Retrieved 2007-09-29.
  25. S2CID 35498132
    .
  26. ISBN 978-0-444-63771-0
    .
  27. ISSN 0016-7606
    .
  28. ISSN 0016-7606
    .
  29. S2CID 37918101
    .
  30. ISBN 978-0-12-803243-5
    , retrieved 2022-08-28
  31. ^
    S2CID 216308379
    .
  32. S2CID 134725972
    .
  33. S2CID 207980627
    .
  34. PMID 27387863
    .
  35. S2CID 213822986
    .
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