Takumi Maekawa’s scientific contributions

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Publications (4)


Smithian-aged (Early Triassic, Early Olenekian) crinoid ossicles from exotic limestone blocks in the lower part of the Thaynes Formation at Crittenden Springs, Elko County, Nevada
  • Article
  • Full-text available

January 2025

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17 Reads

Paleontological Research

Takumi Maekawa

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James F. Jenks

We document the occurrence of Early Triassic (Olenekian) crinoid ossicles in exotic blocks contained within the black limestone unit of the Thaynes Formation, which overlies the Dinwoody Formation at the classic Crittenden Springs Smithian ammonoid locality. Crinoid ossicles include two species, i.e., Holocrinus sp. and Articulata ord., fam., gen. et sp. indet. Furthermore, two co-occurring, age diagnostic conodonts, i.e., Neospathodus pakistanensis and Ns. posterolongatus, constrain the age of the crinoids from the early Smithian to the earliest middle Smithian. This discovery represents the third report of Smithian Holocrinidae in the Panthalassan area and it provides important data for the study of crinoid recovery during the Early Triassic. Fullsize Image

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OLENEKIAN (EARLY TRIASSIC) AMMONOIDS AND CONODONTS FROM SOUTHERN THAILAND OLENEKIAN (EARLY TRIASSIC) AMMONOIDS AND CONODONTS FROM SOUTHERN THAILAND

January 2023

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133 Reads

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Katsuo Sashida

Abstract We document an extensive biostratigraphic investigation of a section of the Phukhaothong Dolomite Member of the marine Triassic Chaiburi Formation (part of the Sibumasu [or Shan-Thai] Block), which is exposed on the north side of an isolated mountain at Khao Thong in the Phatthalung area of southern Thailand. The 104 m+ thick section, consisting of bedded to massive, light grey dolomite, contains ammonoids in the middle to upper parts, and conodonts occur in abundant throughout the section. Seven distinct early Spathian (late Olenekian) ammonoid assemblages, a late Smithian (early Olenekian) conodont zone and three early Spathian conodont zones are recognized in ascending order as follows: ammonoids-Columbites sp. indet. beds, Arctomeekoceras? sp. indet. beds, Tirolites sp. indet. B beds, Tirolites sp. indet. C beds and Tirolites sp. indet. D bed in the Tirolites-Columbites Zone, and the Idahocolumbites cheneyi beds and Idahocolumbites phatthalungensis beds in the Idahocolumbites Zone; conodonts-late Smithian, Hadrodontina aequabilis-Staeschegnathus perrii Zone, early Spathian Icriospathodus crassatus Zone, Triassospathodus symmetricus-Novispathodus anhuiensis Zone and Novispathodus sp. I-Novispathodus sp. J Zone. The age of the primitive ichthyopterygian Thaisaurus chonglakmanii collected from the Idahocolumbites cheneyi beds is constrained to the early Spathian, thus suggesting it is the oldest known ichthyopterygian, because the range of Marcouxia and Idahocolumbites is limited to the Columbites parisianus Subzone of the lower Spathian in the western USA. The Spathian ammonoid faunas exhibit a very strong relationship with other Tethyan as well as eastern Panthalassa faunas in the low paleolatitudes, but bear very little or no relationship with middle and higher latitudinal faunas, suggesting the existence of a strong latitudinal diversity gradient during the Spathian. Late Smithian and early Spathian conodont faunas also exhibit a strong relationship with low paleolatitudinal faunas. Fifty-eight taxa (ammonoids: 26, conodonts: 32) are documented and one new ammonoid species, i.e., Idahocolumbites phatthalungensis, is described.


Smithian (Olenekian, Early Triassic) Conodonts from Ammonoid-Bearing Limestone Blocks at Crittenden Springs, Elko County, Nevada, USA

July 2021

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30 Reads

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11 Citations

Paleontological Research

The ammonoid-bearing limestone blocks at the classic Crittenden Springs ammonoid site belong to the lower part of the Lower Triassic Thaynes Group. These 0.5–1.2 m thick blocks, consisting mainly of bioclastic floatstone and rudstone, contain abundant macro- and micro-fossils such as ammonoids, gastropods, bivalves and scaphopod shells, as well as conodont elements, fish and echinoid remains. Ammonoid and conodont assemblages obtained from three blocks are utilized for biostratigraphical analysis. Twelve informal Smithian ammonoid biostratigraphic intervals from a previous study are condensed into four ammonoid beds, based on the range of age-diagnostic taxa, in ascending order: Meekoceras millardense-M. aff. olivieri beds, Owenites koeneni beds, Anasibirites multiformis bed, and Condensoceras youngi bed. Conodonts recovered from the three blocks consist of 30 species distributed among 15 genera, including one newly described taxon, i.e., Guangxidella minuta Maekawa and Jenks sp. nov. The blocks are divided into two conodont interval zones, i.e., the Novispathodus ex gr. waageni Interval Zone and Nv. pingdingshanensis Interval Zone, based on the first occurrences of their eponymous taxa. Additionally, four conodont range zones, i.e., the Paullella meeki Range Zone, Guangxidella bransoni Range Zone, Scythogondolella milleri Range Zone, and Borinella buurensis Range Zone are recognized, based on the ranges of these four index species. Conodonts within these interval and range zones vary in age from middle Smithian to latest Smithian. The presence of key ammonoid and conodont taxa regarding the Smithian-Spathian boundary (SSB) such as the AW (Anasibirites and Wasatchites) and GXP (Glyptophiceras, Xenoceltites and Pseudosageceras) ammonoid assemblages and the conodonts B. buurensis, Nv. pingdingshanensis and S. milleri demonstrate that the study area is an important reference site for the SSB in the eastern Panthalassa area.


FIGURE 1. A, Generalized map showing location of the Griesbachian ammonoid and nautiloid sites in the Dinwoody Formation (indicated by black dot in Long Canyon) at Crittenden Springs. B, Location of Crittenden Springs area in relation to other western USA Dienerian and Griesbachian localities mentioned in text: 1) Crittenden Springs, 2) Montpelier Canyon, 3) Sleight Canyon, 4) Melrose, 5) Frying Pan Gulch, 6) Candelaria, 7) Willow Spring. Other Triassic exposures mentioned in text: 8) Immigrant Canyon, 9) Windemere Hills, 10) O'Neil Pass, 11) southern end of Pequop Range, 12) Dolly Varden Valley. C. Early Triassic paleoposition of the western USA basin in relation to other world-wide localities discussed in text. (A to C modified from Jenks and Brayard, 2018).
FIGURE 4. A, Gently sloping, east-facing hillside immediately west of ammonoid site with sampled beds demarcated. Nautiloids (five specimens) were found as float within the 2.5 m-thick interval indicated by double-ended arrow (locality NMMNH L-12683) between beds 5 (-1) and 5 (+1), e,g., in B, NMMNH P-81691, Xiaohenautilus mulleni n. sp. and C, NMMNH P-81692, Xiaohenautilus mulleni n. sp. Of these sampled beds, only 5 (+2), a silty limestone bivalve coquina, yielded conodonts.
FIGURE 9. Scatter diagram comparison of H and U, and H/D and U/D for Wordieoceras wordiei (Spath) (gray-shaded circles and triangles) and Wordieoceras mullenae n. sp. (white circles and triangles).
FIGURE 10. Box plot comparison of H/D and U/D for Wordieoceras wordiei (Spath) vs. specimens from Arctic Canada, East Greenland and Siberia. Asterisks indicate values for holotypes of W. wordiei (blue) and W. decipiens (red).
FIGURE 11. A-H, Ophimullericeras paullae n. gen., n. sp. A-C, NMMNH P-81686, paratype, in A, lateral, B, ventral (sub-tabulate venter preserved near end of phragmocone) and C, apertural views. D-F, NMMNH P-81685, paratype, in D, lateral, E, ventral and F, apertural views. G-H, suture lines, in G, NMMNH P-81684, H = 26 mm, H, NMMNH P-81687, H = 29 mm. I-D', Xiaohenautilus mulleni n. sp. I-N, NMMNH P-81692, paratype, in I, lateral (right), J, apertural, K, lateral (left), L, ventral, M, unwhitened left lateral, and N, unwhitened ventral views. O-S, NMMNH P-81691, paratype, in O, lateral (right), P, apertural, Q, lateral (left), and R, ventral views. S, close-up view of venter (Fig. 11P) showing V-shaped hyponomic sinus. T-W, NMMNH P-81693, holotype, in T, lateral (right), U, apertural, V, lateral (left), and W, ventral views. X-Y, D', NMMNH P-81694, paratype, in X, lateral (right), Y, ventral and D', lateral (left). Z-C', NMMNH P-81695, paratype, in Z, lateral (right), A', apertural, B' lateral (left), and C' ventral views. All scale bars = 1 cm.

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Late Griesbachian (early Triassic) ammonoids and nautiloids from the Dinwoody Formation at Crittenden Springs, Elko County, Nevada.

May 2021

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533 Reads

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4 Citations

Abstract—We document a relatively small but very important late Griesbachian ammonoid and nautiloid assemblage from the Dinwoody Formation at Crittenden Springs, Elko County, Nevada. This discovery represents the first significant report of late Griesbachian ammonoids in the low-paleolatitudes of eastern Panthalassa, and it also signifies the first report of Wordieoceras wordiei and two co-occurring taxa outside of the Boreal Realm. This similarity in ammonoid faunas, irrespective of paleolatitude, provides support for the concept of weak latitudinal diversity gradients following the end-Permian extinction. The finding is even more noteworthy given the Dinwoody Formation’s reputation for poor fossil preservation and a near complete absence of documented and identifiable ammonoid and nautiloid occurrences. Consisting of four taxa of which two are newly described, the ammonoid fauna includes Wordieoceras wordiei (Spath), Kyoktites cf. K. hebeiseni Ware and Bucher, Wordieoceras mullenae n. sp. and a new taxon belonging to the Mullericeratidae family, Ophimullericeras paullae n. gen., n. sp. The nautiloids are attributed to a newly described species, i.e., Xiaohenautilus mulleni n. sp., a genus heretofore unknown in eastern Panthalassa but commonly reported from the late Griesbachian of South Primorye and the late Griesbachian/early Dienerian of South China.

Citations (2)


... North America and West Australia became important regions for the study of Lower Triassic sections of conodont biostratigraphy in the second half of the last century, but there have been only a few continuing studies in this century (Sweet et al., 1971;McTavish, 1973;Paull, 1982Paull, , 1988Paull et al., 1997;Orchard and Zonneveld, 2009;Metcalfe et al., 2013). More recently, a couple of related studies of Smithian-Spathian conodont biostratigraphy have been completed (Maekawa and Jenks, 2021;Golding, 2021;Orchard, 2021). ...

Reference:

High-resolution conodont unitary association zonations (UAZs) across the Induan-Olenekian boundary (Lower Triassic): A global correlation
Smithian (Olenekian, Early Triassic) Conodonts from Ammonoid-Bearing Limestone Blocks at Crittenden Springs, Elko County, Nevada, USA
  • Citing Article
  • July 2021

Paleontological Research

... The Thaynes Formation of northeastern Nevada, which consists of various sedimentary rocks such as limestone, mudstone, shale and sandstone beds, contains abundant marine fossils, i.e., ammonoids, gastropods, bivalves, conodonts and echinoderms (Goodspeed and Lucas, 2007;Lucas et al., 2007a, b). These sediments were traditionally divided into the Dinwoody and Thaynes formations and their geological ages were generally defined by age-diagnostic ammonoids and conodonts (Clark, 1957(Clark, , 1959Kummel and Steel, 1962;Sweet et al., 1971;Solien, 1979;Paull, 1980;Carr, 1981;Clark and Carr, 1984;Mullen, 1985;Jenks, 2007;Jenks et al., 2010Jenks et al., , 2013Jenks et al., , 2021Jenks and Brayard, 2018;Maekawa and Jenks, 2021). Considerable biostratigraphical research has been conducted on the ammonoids and conodonts contained within the discontinuous ammonoid-bearing blocks in recent years, but taxonomic work on other groups, e.g. ...

Late Griesbachian (early Triassic) ammonoids and nautiloids from the Dinwoody Formation at Crittenden Springs, Elko County, Nevada.