185 results on '"Conodonta"'
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2. Middle–Upper Ordovician conodonts from the Gunningbland area in central New South Wales with implications for regional correlations.
- Author
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Zhen, Y. Y., Percival, I. G., and Smith, P. M.
- Subjects
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CONODONTS , *FACIES , *CARBONATES , *PROVINCES , *BIOSTRATIGRAPHY , *DEFINITIONS , *LIMESTONE - Abstract
This study documents Middle to Late Ordovician conodont faunas primarily from the Billabong Creek Formation exposed in the Gunningbland area located west of Parkes and northwest of Forbes in central New South Wales. Forty-four identifiable conodont species recovered from 105 limestone samples in this area form the basis of the most complete biostratigraphic succession in shallow-water facies known through this interval from Australia. Four conodont biozones are recognised, extending from the middle Darriwilian Histiodella holodentata–Eoplacognathus pseudoplanus and Eoplacognathus suecicus biozones, through the upper Darriwilian Pygodus serra Biozone, to the Pygodus anserinus Biozone spanning the uppermost Darriwilian to basal Sandbian interval. A lower to middle Sandbian carbonate gap coincides with an unzoned interval, followed by the successively younger Belodina compressa, Phragmodus undatus and Taoqupognathus blandus conodont biozones in the upper Sandbian to lower Katian. The T. blandus Biozone directly correlates with the detailed conodont biozonation established in Katian limestones of the Molong Volcanic Belt further east. These age determinations provide much improved precision for correlation within Phases 2 and 3 in the mineral-rich Macquarie Volcanic Province. Analysis of conodont biofacies data supports an enhanced understanding of the geological evolution of the Macquarie Volcanic Province by interpreting the interplay between volcanic activity and carbonate deposition. Conodont studies in the Billabong Creek Formation of the Gunningbland area reveal the only known biostratigraphic succession in Australia that extends continuously from the middle Darriwilian to basal Sandbian. Three Late Ordovician (late Sandbian to early Katian) conodont biozones in the upper Billabong Creek Formation correlate precisely with carbonates of the Molong Volcanic Belt to the east. Revised stratigraphic definitions of the Billabong Creek and Gunningbland formations are provided. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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3. The Fossil Record of Conodonts in Greece
- Author
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Koukousioura, Olga, Dimou, Vasiliki–Grigoria, and Vlachos, Evangelos, editor
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- 2022
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4. DEVONIAN CONODONTS FROM SPITI HIMALAYA, INDIA
- Author
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A. D. AHLUWALIA, V.J. GUPTA, K. J. BUDUROV, and S. S. KANWAR
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Conodonta ,Biostratigraphy ,Chronostratigraphy ,Devonian ,Himalaya . ,Geology ,QE1-996.5 ,Paleontology ,QE701-760 - Abstract
The present paper describes the lower Upper Devonian conodont fauna from the upper units of Muth Formation, Spiti Valley, Himalaya.
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- 2023
5. Chaetognath grasping spines from the Devonian of Poland: their structure and geochemistry.
- Author
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WIERZBOWSKI, HUBERT and BŁAŻEJOWSKI, BŁAŻEJ
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SEDIMENT-water interfaces , *GEOCHEMISTRY , *SPINE , *CALCIUM phosphate , *ANALYTICAL geochemistry , *IRON - Abstract
Previously unidentified small (up to 1.3 mm in length), gently curved hollow spines composed of calcium phosphate and derived from the upper Famennian (Devonian) of the Holy Cross Mountains in central Poland are described. They are similar to the type species of Phakelodus, but show some distinct morphological differences, therefore, have been included into Phakeloides polonicus gen. et sp. nov. The studied specimens of that species show relatively massive mineral structure characterized by significant porosity with well-preserved major structural features. The outer layer of the spines is, in contrary, fragmentarily preserved, and exposes distinct mosaic-like ornamentation of the surface of the middle layer, which consists of obliquely arranged, shallow furrows. Geochemical analyses of the Devonian Phakeloides polonicus gen. et sp. nov. spines have revealed the presence of a weaker mineralized structure, compared to conodont apatite, composed of a diagenetic phosphate phase. It is characterized by moderate cathodoluminescence intensity, elevated concentrations of iron and sulphur as well as decreased concentrations of strontium, calcium, and phosphorus. The "Orsten" type, early diagenetic phosphatization of the outer layer of the spines is not observed in studied specimens of Phakeloides polonicus gen. et sp. nov., contrary to the previously investigated Furongian (Cambrian) material. This points to the low rate of diagenetic phosphatization, which was likely enabled by very slow sedimentation and long residence time of the spines close to sediment-water interface at varying redox conditions and significant flux of phosphate ions. [ABSTRACT FROM AUTHOR]
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- 2023
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6. A review of the Late Triassic conodont conundrum: survival beyond biotic perturbations.
- Author
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Ruban, Dmitry A.
- Abstract
Significant advance in the understanding of the Late Triassic evolution of conodonts and their final disappearance has been made recently. However, the relevant information is rather fragmented and inconsistent. Its critical assessment is undertaken in order to synthesise the new lines of evidence. The final disappearance of conodonts, which should be distinguished from their regional disappearances and precedent diversity changes, occurred at the Rhaetian–Hettangian transition. It was not preceded by a gradual decline: conodonts were able to diversify in the Late Triassic and to survive several biotic crises/turnovers. Their diversity dynamics corresponded (at least, partly) to the eustatic fluctuations similarly to how this occurred during the entire history of this fossil group. [ABSTRACT FROM AUTHOR]
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- 2022
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7. Conodont Biostratigraphy of Ordovician Deep-Water Turbiditic Sequences in Eastern Australia—A New Biozonal Scheme for the Open-Sea Realm.
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Zhen, Yong Yi, Percival, Ian G., Gilmore, Phil, Rutledge, Jodie, and Deyssing, Liann
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SILICICLASTIC rocks , *SILTSTONE , *BIOSTRATIGRAPHY , *CHERT , *ORDOVICIAN Period , *CONODONTS , *PALEOBIOGEOGRAPHY - Abstract
Ordovician conodonts representing 28 genera and 28 named and three unnamed species were identified from 740 chert and siliceous siltstone spot samples (>3 000 thin sections) from deep-water turbiditic sequences of the Lachlan Orogen in central and southern New South Wales, Australia. Based on these faunas, a new conodont biozonal scheme has been established to divide the Ordovician turbiditic successions of the Lachlan Orogen into 12 superbiozones and biozones. They are (in ascending order) the Paracordylodus gracilis Superbiozone (including the Prioniodus oepiki Biozone), Periodon flabellum Superbiozone (including the Oepikodus evae Biozone in the lower part), Periodon hankensis Biozone, Periodon aculeatus Superbiozone (including the Histiodella labiosa, Histiodella holodentata, Histiodella kristinae, Pygodus serra and Pygodus anserinus biozones) and the Periodon grandis Biozone. The Pygodus anserinus Biozone is divided further into the lower and upper subbiozones. This new conodont biozonation scheme spanning the upper Tremadocian to middle Katian interval permits precise age-dating and correlation of deep-water siliciclastic rocks that characterize the Ordovician Deep-Sea Realm regionally and internationally. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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8. Anisian (Middle Triassic) Conodonts of the Kocaeli Triassic, Western Turkey.
- Author
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Kılıç, Ali Murat
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CONODONTS , *SPECIES , *PENINSULAS - Abstract
The present study of Anisian (Middle Triassic) conodonts from the Kocaeli Peninsula (western Turkey) encompasses over 10 species of the families Gondolellidae and Gladigondolellidae, providing Early and Middle Triassic time constraints, Chiosella timorensis (Nogami, 1968); Cornudina oezdemirae Gedik, 1975; Gladigondolella tethydis (Huckriede, 1958); Neostrachanognathus tahoensis Koike, 1998; Paragondolella aegaea (Bender, 1970); Paragondolella bulgarica Budurov and Stefanov, 1975; Nicoraella kockeli (Tatge, 1956); P. hanbulogi (Sudar and Budurov, 1979), and Gladigondolella sp. A. Newly established are Paragondolella hirschii n. sp. Kılıç and Budurov; P. praecornuta n. sp. Kılıç, Budurov, Petrunova and Mir0103uţ0103; and P. ebruae n. sp. Kılıç. The Kocaeli Anisian conodonts show a faunal affinity with Bulgaria. The present Anisian fauna is characteristic of the Tethys. The strong homeomorphy that characterizes the Anisian in western North America is discussed. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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9. CONODONT FAUNA FROM THE ROTELLIFORME, MEEKI AND OCCIDENTALIS ZONES (MIDDLE TRIASSIC) OF HUMBOLDT RANGE, NEVADA, WESTERN-NORTH AMERICA
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ALDA NICORA and SANDOR KOVACS
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Stratigraphy ,Conodonta ,Middle Triassic ,Anisian/Ladinian ,Nevada (USA) ,Geology ,QE1-996.5 ,Paleontology ,QE701-760 - Abstract
The conodont fauna of the Rotelliforme, Meeki, Occidentalis and lower Subasperum zones of Nevada (Humboldt Range) is here described. The first three zones represent, by means of the American authors, the Upper Anisian of North America, while at the base of the Subasperum Zone is located the Anisian/Ladinian boundary. Three species—groups of conodonts have been emended and revised, they are: Gondolella constricta Mosher & Clark, Gondolella mombergensis mombergensis Tatge and Gondolella mombergensis longa (Budurov & Stefanov). Comparisons with the possible coeval faunas of epicontinental sequences from Europe have been discussed. Within the conodont fauna, the main change has been noted at the base of the Occidentalis Zone. On the base of the conodont fauna, the Anisian/ Ladinian boundary at the base of the Occidentalis Zone seems to be the most supported in Nevada.
- Published
- 2020
10. UPPER DEVONIAN CONODONTS FROM LADAKH, HIMALAYA, INDIA
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V. J. GUPTA and S. UPPAL
- Subjects
Conodonta ,Biostratigraphy ,Chronostratigraphy ,Devonian ,Himalaya. ,Geology ,QE1-996.5 ,Paleontology ,QE701-760 - Abstract
The preserit paper describes Upper Devonian conodont fauna from the black and bluish limestone succession lying immediately above the Muth Quartzite exposed near the village Tanze, Luneak valley, Ladakh.
- Published
- 2020
11. PERMIAN-TRIASSIC BOUNDARY AND EARLY TRIASSIC CONODONTS FROM THE SOUTHERN ALPS, ITALY
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MARIA CRISTINA PERRI and MIRELLA ANDRAGHETTI
- Subjects
Conodonta ,Taxonomy ,Biostratigraphy ,Permian/Triassic ,Southern Alps ,Italy. ,Geology ,QE1-996.5 ,Paleontology ,QE701-760 - Abstract
The Bellerophon (Late Permian) and Werfen (Lower Triassic) Formations were investigated on the basis of conodonts. Fifteen sections were sampled from Carnic Alps and Dolomites area in the Southern Alps. Ten were productive. The Bellerophon Formation yielded a few specimens of Hindeodus typicalis, Ellisonia agordina and Ellisonia sp. In the Werfen Formation were collected Hindeodus typicalis, Ellisonia agordina, E. triassica, Hadrodontina anceps, Xaniognathus gradatus, Isarcicella isarcica, Pachycladina obliqua, Ellisonia delicatula, Neospathodus triangularis. In describing the conodont fauna, multielement taxonomy is applied. Ellisonia agordina is a new species found at the top of the Bellerophon Formation and from the Tesero to the Siusi Members of the Werfen Formation, i, e. at the Permian — Triassic boundary and in the Lower Triassic. The apparatus of this new species is described. In the Southern Alps the range of Hindeodus typicalis, previously known in the Werfen Formation, extends down into the uppermost Bellerophon Formation. All species confirm the ranges found elsewhere in the world. On the basis of only the conodont fauna, it is not possible as yet to recognize the position of the Permian — Triassic boundary more precisely in the Bellerophon/Werfen Formations in the Southern Alps. It is obvious, however, that the recovery of Isarcicella isarcica allows the certain identification of the Triassic.
- Published
- 2020
12. Wenlock-Ludlow boundary sediments on Chernov uplift (Arctic region of Russia).
- Author
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MATVEEV, VLADIMIR A., BEZNOSOVA, TATIANA M., and GÖMZE, LÁSZLÓ A.
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RIVER sediments , *SEDIMENTS , *WATERSHEDS , *BRACHIOPODA , *CONODONTS , *TUNDRAS - Abstract
The article presents the results of a study of Wenlock-Ludlow boundary sediments in the river Padimeytyvis basin at Chernov uplift using paleontological, lithological and chemostratic methods. The results of paleontological studies allowed attributing to the Wenlock the carbonate stratum of the upper part of the section along the stream Bezymjannyi and establishing Wenlock-Ludlow boundary only in the section of the river Padimeytyvis. The results of studying the isotope δ13Ccarb. in Wenlock-Ludlow boundary sediments are also presented. In the upper part of the section along the stream Bezymyanny a positive C-isotopic shift of the curve which possibly marks the late Wenlock global biotic event of Mulde was observed. Keywords: Ludlow, Wenlock, conodonts, brachiopods, Arctic region, Timan-Northern Ural region, isotope δ13Ccarb. [ABSTRACT FROM AUTHOR]
- Published
- 2020
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13. A new species of the conodont genus Siphonodella Branson & Mehl (late Tournaisian)
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Andrey V. Zhuravlev
- Subjects
Conodonta ,new species ,Siphonodella carinata n. sp. ,Lower Carboniferous ,Tournaisian. ,Geology ,QE1-996.5 - Abstract
A new upper Tournaisian (Lower Carboniferous) siphonodellid conodont species Siphonodella carinata n. sp. is described. The material comes from the shallow-water carbonate sediments of the Pechora Swell (Timan-Pechora region or NE of European Russia). The co-occurrence of conodonts Hindeodus cristulus (Youngquist & Miller), Bispathodus stabilis (Branson & Mehl) Morphotype 1, Polygnathus longiposticus Branson & Mehl and Pseudopolygnathus nodomarginatus (Branson) suggests the late Tournaisian (Lower Siphonodella crenulata Zone) age of the deposits. Morphologically the new species is similar to Siphonodella semichatovae Kononova & Lipnjagov and S. ludmilae Zhuravlev & Plotitsyn, but differs in possessing three rostral ridges at the late stages of ontogeny and Class III symmetry. The presence of the shallow-water siphonodellids Siphonodella bella Kononova & Migdisova and S. quasinuda Gagiev, Kononova & Pazuhin in the upper part of the Tournaisian is detected for the first time.
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- 2017
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14. DEVONIAN CONODONTS FROM SPITI HIMALAYA, INDIA
- Author
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AHLUWALIA, A. D., GUPTA, V.J., BUDUROV, K. J., and KANWAR, S. S.
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Conodonta ,Biostratigraphy ,Chronostratigraphy ,Devonian ,Himalaya - Abstract
The present paper describes the lower Upper Devonian conodont fauna from the upper units of Muth Formation, Spiti Valley, Himalaya.
- Published
- 2023
15. Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
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Nicholas J. Hogancamp, James E. Barrick, and Richard E. Straus
- Subjects
Conodonta ,Idiognathodus ,morphometrics ,Pennsylvanian ,Gzhelian ,North America ,Midcontinent ,Fossil man. Human paleontology ,GN282-286.7 ,Paleontology ,QE701-760 - Abstract
A new morphometric approach was developed to study morphological variation within P1 elements commonly referred to as Idiognathodus simulator, which was selected to be the biostratigraphic marker for the base of the global Gzhelian Stage (Carboniferous). This new approach combines landmark-based geometric morphometrics with eigen analyses to analyze shape variation within P1 elements of the I. simulator group, and could be used to analyze shape variation in other morphologically similar conodont groups. Specimens analyzed were obtained from three sections of the early Gzhelian Heebner Shale of the Oread cyclothem in the North American Midcontinent region, the cyclothem from which I. simulator was originally named. This analysis shows that the I. simulator group comprises a set of at least five species with asymmetrical P1 element pairs, relatively short adcarinal ridges, and a variably developed eccentric groove. Species discrimination is based on the presence of caudal and rostral lobes, character of the adcarinal ridges, and platform shape. The species I. simulator is restricted to P1 elements with a caudal adcarinal ridge that is isolated from the caudal platform margin. Idiognathodus lateralis sp. nov. is erected to include P1 elements with a caudal adcarinal ridge that is not isolated from the caudal platform margin.
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- 2016
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16. New group of the Early Palaeozoic conodont-like fossils
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Hubert Szaniawski
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Cambrian ,Conodonta ,Chaetognatha ,evolution ,Ordovician ,paraconodonts. ,Geology ,QE1-996.5 - Abstract
The paper is devoted to the Upper Cambrian and Tremadocian organophosphatic microfossils which were hitherto treated as conodonts and assigned mainly to the genera Coelocerodontus and Viirodus. Individual elements of the fossils, similarly to the elements of conodonts, belonged originally to the multi-element apparatuses. Present studies, based mainly on the collections from Sweden, Poland (core sections), Estonia and Kazakhstan, show that despite the similarities of their individual elements to conodonts, they significantly differ from them in the inner structure, as well as in the construction of the apparatuses composed of them. Elements of their apparatuses are matched in shape to each other and certainly functioned in conjunction, while those belonging to the euconodont apparatuses are usually differentiated in shape and usually functioned in separation. All fossils of this group are provisionally named coelocerodonts in this paper. Their individual elements, as well as the apparatuses composed of them, are similar in construction to those of the genus Phakelodus, which is an ancestor of chaetognaths.
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- 2015
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17. Origin and evolution of the Early Ordovician conodont genus Prioniodus Pander, 1856 — New evidence from South China.
- Author
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Zhen, Yong Yi, Zhang, Yuan-Dong, Chen, Zhong-Yang, and Wang, Long-Wu
- Subjects
- *
CONODONTS , *WATER depth - Abstract
A conodont fauna of late Tremadocian to early Floian age (Early Ordovician) is documented from the Yinchufu Formation of Zhejiang Province, South China. It is characterized by the occurrence of two species of Prioniodontidae, a new species of Prioniodus and Acodus triangularis. Prioniodus antiquus sp. nov. may represent the most primitive species of Prioniodus , which is one of the earliest conodont genera with a ramiform—pectiniform apparatus. Based on the review of nearly 200 species originally assigned to Prioniodus , six multielement species are confirmed to belong to this genus. Morphological changes of these six species shows that they form an evolutionary lineage directly evolved from an adentate species, likely Acodus triangularis which has been reported from South China, Australia and from the Precordillera of western Argentina. Origination of the ramiform—pectiniform apparatuses as represented by the appearances of Prioniodus through late Tremadocian to Floian of the Early Ordovician might be a major response of the 'conodont animals' to occupy and adapt to the increasingly diversified environments in the shelf and slope settings. The biofacies distribution of the six Prioniodus species indicates that Prioniodus might have originated in deep-water slope settings and progressively spread into distal and then interior shelves in the late Tremadocian and diversified in the Floian, with Prioniodus amadeus possibly representing a relict species that survived into the Middle Ordovician and was restricted to shallow water environments. • A case study investigates the origination of the ramiform—pectiniform apparatus. • The grouping of the six Prioniodus species and their evolutionary relationships are discussed. • Prioniodus probably originated in deep-water environments and progressively spread into distal and then interior shelves. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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18. CONODONTS FROM THE LOWER TRIASSIC SEQUENCE OF CENTRAL DOLPO, NEPAL
- Author
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ALDA NICORA
- Subjects
Stratigraphy ,Conodonta ,Lower Triassic ,Scythian ,Central Dolpo ,Nepal. ,Geology ,QE1-996.5 ,Paleontology ,QE701-760 - Abstract
In the present paper, the conodont fauna from three detailed sections surveyed in the Lower Triassic sequence of Central Dolpo, Nepal (Tarap-Atali area) is illustrated. Combining faunas from the three sections, it was possible to recognize a succession of faunal events that covers most of the Scythian and the Lower Anisian. In the whole, 11 faunas have been recognized and discussed.
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- 2017
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19. FRASNIAN AND VISEAN-NAMURIAN CONODONT FAUNAS AT PRAPROTNO, SLOVENIA
- Author
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TEA KOLAR-JURKOVSEK and BOGDAN JURKOVSEK
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Conodonta ,Devonian ,Carboniferous ,Slovenia. ,Geology ,QE1-996.5 ,Paleontology ,QE701-760 - Abstract
Conodont faunas from the limestone pebbles of the Upper Paleozoic Conglomerate at Praprotno, Slovenia demonstrate the presence of two faunas. The older fauna, marked by Palmatolepis surecta and Polygnathus decorosus is indicative of the Frasnian stage (Upper Devonian). The younger fauna is dominated by Gnathodus bilineatus and contains Lochriea commutata and L. nodosa. This fauna is characteristic of the Late Visean-Namurian (Lower Carboniferous).
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- 2017
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20. PERMIAN STRATIGRAPHY IN THE NORTHERN KARAKORUM, PAKISTAN
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MAURIZIO GAETANI, LUCIA ANGIOLINI, EDUARDO GARZANTI, FLAVIO JADOUL, ERNST YA. LEVEN, ALDA NICORA, and DARIO SCIUNNACH
- Subjects
Permian ,Stratigraphy ,Foraminifera ,Coelenterata ,Brachiopoda ,Bivalvia ,Conodonta ,Sandstone petrography ,Microfacies ,Paleogeography ,Karakorum ,Pakistan. ,Geology ,QE1-996.5 ,Paleontology ,QE701-760 - Abstract
The stratigraphical data collected during four geological expeditions to the Northern Karakorum (1996,1991,1992a,1992b) are discussed. The sedimentary succession has been classified by 9 formations, here formalised, and subdivided into members and lithozones. The biochronology has been established on fusulinids, brachiopods, and conodonts. Several plates illustrate the most significant fossil species as well as the litho- and microfacies. The sedimentary succession may be roughly subdivided into three parts. The lower part consists of terrigenous rocks, mostly pelitic and less frequently arenaceous(quartzarenites with thick arkose intervals during the latest Asselian-early Sakmarian). They are evidence of a continental to coxtal environment, with short term marine ingressions. The second part begins with the Sakmarian, when the marine environment spread over most of the studied area. Bioclastic sand bars with brachiopods and crinoids at the base are followed by huge fusulinid packages. In Hunza oolitic bars and dolostone peritidal cycles also follow. The carbonate ramp is often polluted by terrigenous sediments, especially westwards. Temporary arenaceous spillovers (quartzarenites), often linked to minor sedimentation gaps, occur both westwards in the Baroghil area, and eastwards in the Hunza-Shimshal area. In the centre, in the Upper Karambar valley, a large gap most probably occurs, with reappearance of the sedimentation only with the dolostones of the Upper Permian. These erosional episodes with arenaceous spillovers are interpreted as being linked to rifting events of the Neotethys opening, active southwards. The third part of rhe succession concerns the Late Permian. Towards the end at the Murgabian or at the beginning of the Midian, the Northern Karakorum is subdivided into two major areas. To the west, after a transgressive episode with ironstone deposition, a wide peritidal carbonate platform spread over from Baroghil to Chillinji in Karambar and the Pasu area in Hunza. This palaeogeographic pattern extends up to the Triassic. However, biostratigraphic control is poor. Instead to the north-east, a progressive sinking of the slope is observed, with spreading of deeper environments and cherty limestone deposition. The down-warping is activated by block-faulting resulting in huge megabreccia bodies interbedded with the cherty limestones. During the Dzhulfian, significant clay inputs dilute the carbonate mud accumulation and shales are dominant around the Permian-Triassic boundary. Pelagic carbonate sedimentation gradually recovers from the Smithian onward. The Permian of the Karakorum is the sedimentary evidence of the passive margin of a lithospheric block, detached from the Gondwana continent during the Permian, that will later migrate towards the centre of the Paleo-Tethys, along with other lithospheric blocks of the Mega Lhasa plate.
- Published
- 2017
- Full Text
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21. Upper Devonian conodonts of northeastern European Russia.
- Author
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Ovnatanova, N., Kononova, L., Kolesnik, L., and Gatovsky, Yu.
- Abstract
The conodont succession in the Upper Devonian facially different sections of northeastern European Russia (Chernyshev Ridge, Subpolar and Polar Urals, Pai-Khoi) are studied. The sections are subdivided and correlated taking into account the global standards for stages. The Frasnian Montagne Noire zonation (Klapper, 1989) is used for the first time for northeastern European Russia; the authors correlated this zonation with the scale of Ziegler and Sandberg (1990). Famennian deposits are subdivided using scale of Ziegler and Sandberg (1984) and miospore zonation. The age of local geological units (formations) is specified; the formations of different regions of northeastern European Russia are correlated to each other and to the regional subdivisions of EEP and Southern Urals. A total of 93 species of Ancyrodella, Mesotaxis, Palmatolepis, Polygnathus, and Zieglerina are described. Two new species Ctenopolygnathus parallelus sp. nov. and Polygnathus masonae sp. nov. are distinguished and five species are described in the open nomenclature. Special chapter is devoted to the phylomorphogenesis of Ancyrodella. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
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22. A new species of the conodont genus Siphonodella Branson & Mehl (late Tournaisian).
- Author
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Zhuravlev, Andrey V.
- Subjects
- *
CONODONTS , *TOURNAISIAN Stage , *ONTOGENY , *ANIMAL morphology , *CARBONATES , *SEDIMENTATION & deposition - Abstract
A new upper Tournaisian (Lower Carboniferous) siphonodellid conodont species Siphonodella carinata n. sp. is described. The material comes from the shallow-water carbonate sediments of the Pechora Swell (Timan-Pechora region or NE of European Russia). The co-occurrence of conodonts Hindeodus cristulus (Youngquist & Miller), Bispathodus stabilis (Branson & Mehl) Morphotype 1, Polygnathus longiposticus Branson & Mehl and Pseudopolygnathus nodomarginatus (Branson) suggests the late Tournaisian (Lower Siphonodella crenulata Zone) age of the deposits. Morphologically the new species is similar to Siphonodella semichatovae Kononova & Lipnjagov and S. ludmilae Zhuravlev & Plotitsyn, but differs in possessing three rostral ridges at the late stages of ontogeny and Class III symmetry. The presence of the shallow-water siphonodellids Siphonodella bella Kononova & Migdisova and S. quasinuda Gagiev, Kononova & Pazuhin in the upper part of the Tournaisian is detected for the first time. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
23. Icriodus marieae, a new icriodontid conodont species from the Middle Devonian.
- Author
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Suttner, Thomas, Kido, Erika, and Suttner, Andreas
- Abstract
Copyright of Paläontologische Zeitschrift is the property of Springer Nature and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2017
- Full Text
- View/download PDF
24. Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America.
- Author
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HOGANCAMP, NICHOLAS J., BARRICK, JAMES E., and STRAUSS, RICHARD E.
- Subjects
- *
MORPHOMETRICS , *CONODONTS , *GZHELIAN Stage (Geology) - Abstract
A new morphometric approach was developed to study morphological variation within P1 elements commonly referred to as Idiognathodus simulator, which was selected to be the biostratigraphic marker for the base of the global Gzhelian Stage (Carboniferous). This new approach combines landmark-based geometric morphometrics with eigen analyses to analyze shape variation within P1 elements of the I. simulator group, and could be used to analyze shape variation in other morphologically similar conodont groups. Specimens analyzed were obtained from three sections of the early Gzhelian Heebner Shale of the Oread cyclothem in the North American Midcontinent region, the cyclothem from which I. simulator was originally named. This analysis shows that the I. simulator group comprises a set of at least five species with asymmetrical P1 element pairs, relatively short adcarinal ridges, and a variably developed eccentric groove. Species discrimination is based on the presence of caudal and rostral lobes, character of the adcarinal ridges, and platform shape. The species I. simulator is restricted to P1 elements with a caudal adcarinal ridge that is isolated from the caudal platform margin. Idiognathodus lateralis sp. nov. is erected to include P1 elements with a caudal adcarinal ridge that is not isolated from the caudal platform margin. [ABSTRACT FROM AUTHOR]
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- 2016
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25. Drepanoistodus svendi Rasmussen & Eriksson & Lindskog 2021, sp. nov
- Author
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Rasmussen, Jan Audun, Eriksson, Mats E., and Lindskog, Anders
- Subjects
Conodonta ,Drepanoistodus ,Animalia ,Drepanoistodontidae ,Biodiversity ,Drepanoistodus svendi ,Chordata ,Taxonomy ,Distacodontina - Abstract
Drepanoistodus svendi sp. nov. urn:lsid:zoobank.org:act: 0921F27A-ECF6-498C-8943-4DEB96CFBB38 Fig. 6I–L Drepanoistodus aff. basiovalis (Sergeeva) - Rasmussen 2001: 73–74, pl. 5 fig. 17.— Mellgren et al. 2012: fig. 5u. Diagnosis A Drepanoistodus species characterised by a geniculate element with a recurved cusp and distinct keels on both the cusp and the upper margin of the base. Weakly curved but distinct carinas are developed on both sides of the cusp, especially well developed on the inner side. Etymology Named after the Danish palaeontologist and conodont specialist Svend S. Stouge, Natural History Museum of Denmark, University of Copenhagen. Material examined Five geniculate elements including three from the Lynna section. Holotype, geniculate element (Fig. 6J–K); LO 12483T. Type locality River bank near the mouth of Lynna River, village of Kolchanovo, St. Petersburg region, Russia (60°00′39″ N, 32°33′49″ E). Type stratum Approximately 40 cm below the local top of the Volkhov Formation, sample LY 12-14, ca 20 cm above the base of the Lenodus variabilis Zone sensu Lindskog et al. (2020). Description Cusp is recurved (bent weakly downward), with distinct keels developed along the anterior (upper) and posterior (lower) margins. A median, longitudinal, weakly curved carina is developed on both sides of the cusp, most distinct on the inner side of the cusp. Cusp is almost twice as long as the upper margin of the cusp; the mean ratio between the length of the free upper margin and the free cusp (Fig. 3) is ca 0.55 with a standard deviation of 0.13. Basal margin varies from rounded (convex) to almost straight. A distinct keel is developed on the upper margin. Anterior margin is rounded or weakly rounded (convex). Angle A (Fig. 3) between the cusp and upper margin of the base varies considerable with a mean of 24° and standard deviation of 6.9 (Fig. 5B). Zone. L. Same specimen as I in outer view. M–O. Drepanoistodus viirae sp. nov. M. LO 12484T, holotype, inner view, sample LY12-31, interzone (“uncertain interval”) between the Lenodus variabilis Zone and the Yangtzeplacognathus crassus Zone sensu Lindskog et al. (2020). N. Same specimen as M in outer view. O. LO 12485t, inner view, sample LY 12-31, interzone (“uncertain interval”) between the Lenodus variabilis Zone and the Yangtzeplacognathus crassus Zone sensu Lindskog et al. (2020). P–Q. Drepanoistodus aff. basiovalis (Sergeeva, 1963), LO 12486t, inner and outer view, respectively, sample LY12-9, L. antivariabilis Zone. R –S. Drepanoistodus stougei Rasmussen, 1991, LO 12487t, inner and outer view, respectively, sample LY12-13, L. variabilis Zone. T. Drepanoistodus cf. suberectus (Branson & Mehl, 1933), LO 12488t, inner view, sample LY14-2, Y. crassus Zone. Scale bar = 200 μm (all specimens illustrated at same scale). Remarks Drepanoistodus svendi sp. nov. is distinguished from all the other Drepanoistodus species in the present study by the recurved cusp and the curved carina on each side of the cusp. Like D. iommii sp. nov., it is characterised by a clearly longer upper margin of the base compared to the cusp length than in D. basiovalis. The D. svendi sp. nov. population is located in the lower, right quadrangle of the PCA plot, far from any other species of Drepanoistodus, and the biplot vectors representing the recurved cusp and the curved carina point in this direction (Fig. 4). The PERMANOVA test on the first seven PCA axis shows that the probability that the D. basiovalis and D. svendi sp. nov. populations are the same, is exceedingly low (p (same) = 1.00E- 04). Occurrence The lower part of the L. variabilis Zone (samples LY12-13, LY12-14). Moreover, D. svendi sp. nov. has been recorded from Steinsodden, Norway, from the top of the B. norrlandicus – D. stougei Zone and the base of the overlying B. medius – H. holodentata Zone, which correlate with the middle part of the L. variabilis Zone (as D. aff. basiovalis sensu Rasmussen 2001), and from the L. pseudoplanus Zone or E. suecicus Zone at the island Osmussaar, Estonia (Mellgren et al. 2012; reported as D. aff. basiovalis)., Published as part of Rasmussen, Jan Audun, Eriksson, Mats E. & Lindskog, Anders, 2021, Middle Ordovician Drepanoistodus (Vertebrata, Conodonta) from Baltica, with description of three new species, pp. 106-134 in European Journal of Taxonomy 774 on pages 122-123, DOI: 10.5852/ejt.2021.774.1533, http://zenodo.org/record/5557148, {"references":["Rasmussen J. A. 2001. Conodont biostratigraphy and taxonomy of the Ordovician shelf margin deposits in the Scandinavian Caledonides. Fossils and Strata 48: 1 - 180.","Mellgren J. I. S., Schmitz B., Ainsaar L., Kirsimae K. & Eriksson M. E. 2012. Conodont dating of the Middle Ordovician breccia cap-rock limestone on Osmussaar Island, northwestern Estonia. Estonian Journal of Earth Sciences 61: 133 - 148. https: // doi. org / 10.3176 / earth. 2012.3.01","Lindskog A., Eriksson M. E., Rasmussen J. A., Dronov A. & Rasmussen C. M. O. 2020. Middle Ordovician carbonate facies development, conodont biostratigraphy and faunal diversity patterns at the Lynna River, northwestern Russia. Estonian Journal of Earth Sciences 69: 37 - 61. https: // doi. org / 10.3176 / earth. 2020.1.03","Sergeeva S. P. 1963. [Conodonts from the Lower Ordovician in the Leningrad region.] Paleontologicheshij Zhurnal 1963 (2): 93 - 108. [In Russian.]","Rasmussen J. A. 1991. Conodont stratigraphy of the Lower Ordovician Huk Formation at Slemmestad, southern Norway. Norsk Geologisk Tidsskrift 71: 265 - 88.","Branson E. B. & Mehl M. G. 1933. Conodont studies no. 2; conodonts from Joachim (Middle Ordovician) of Missouri; from the Plattin (Middle Ordovician) of Missouri; from the Maquoketa-Thebes (Upper Ordovician) of Missouri; a study of Hinde's types of conodonts preserved in the British Museum. Missouri University Studies 8: 77 - 167."]}
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- 2021
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26. Drepanoistodus viirae Rasmussen & Eriksson & Lindskog 2021, sp. nov
- Author
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Rasmussen, Jan Audun, Eriksson, Mats E., and Lindskog, Anders
- Subjects
Conodonta ,Drepanoistodus ,Animalia ,Drepanoistodontidae ,Biodiversity ,Drepanoistodus viirae ,Chordata ,Taxonomy ,Distacodontina - Abstract
Drepanoistodus viirae sp. nov. urn:lsid:zoobank.org:act: AD10D9B3-9802-4DAC-97C0-B44EB8DE195D Fig. 6M–O Drepanoistodus basiovalis (Sergeeva, 1963) – Löfgren 2000b: fig. 4p; 2003: fig. 7aa. — Lindskog et al. 2020: fig. 7v–w. partim Drepanoistodus cf. basiovalis – Rasmussen 2001: 73, pl. 5 fig. 16 (only). Drepanoistodus cf. stougei Rasmussen, 1991 – Rasmussen 2001: 76, pl. 6 fig. 12. Drepanoistodus aff. suberectus (Branson & Mehl, 1933) – Mellgren & Eriksson 2010: fig. 7f. aff. Drepanoistodus basiovalis – Feltes & Albanesi 2013: fig. 3.12. ? partim Drepanoistodus basiovalis – Zhen 2020: 18–19, fig. 7b (only). Diagnosis A Drepanoistodus species characterised by a geniculate element with a wide, straight, compressed cusp and a very short base, where the free cusp typically is ca 4 times longer than the upper margin of the base. Etymology Named after the Estonian palaeontologist and conodont specialist Viive Viira, Tallinn University of Technology, Estonia. Material examined Nine geniculate elements including five from the Lynna section. Holotype, geniculate element (Fig. 6M–N); LO 12484T. Type locality River bank near the mouth of Lynna River, village of Kolchanovo, St. Petersburg region, Russia (60°00′39″ N, 32°33′49″ E). Type stratum Approximately 15 cm above the local base of the Sillaoru Formation, sample LY 12-31. Lower part of the 90 cm thick interzone (“uncertain interval”) between the Lenodus variabilis Zone and the Yangtzeplacognathus crassus Zone sensu Lindskog et al. (2020). Description Cusp is reclined, wide (from upper to lower margin) and straight, with keels developed along the anterior (upper) and posterior (lower) margins. A weak, median, longitudinal carina is developed on the inner side of the cusp. Occasionally, the carina may be distinct. Basal margin is weakly rounded or straight. A distinct keel is developed on the upper margin. Anterior margin is rounded or weakly rounded (convex). Angle A (Fig. 3) between the cusp and upper margin of the base is ca 30° (mean) with a standard deviation of 4.3 (Fig. 5B), and mean ratio between length of the free upper margin and the free cusp is ca 0.25 with a standard deviation of 0.05. Remarks Drepanoistodus viirae sp. nov. is situated in the lower left quadrangle of the PCA plot (Fig. 4). Like D. basiovalis, it is clearly separated from D. iommii sp. nov. and D. svendi sp. nov., whereas it partly overlaps with the D. basiovalis population, when only the PC 1 (x) and PC 2 (y) axis is plotted. The vectors in the biplot reinforce that D. viirae sp. nov. is characterised by a convex basal margin, a weakly developed carina and a short upper margin on the base (= low b/c value), the latter because it is situated in the opposite direction of the b/c vector, as seen in Fig. 4. The partial overlap with D. basiovalis occurs because the two species share some characters. A significant difference, however, is that D. viirae sp. nov. has a relatively shorter upper margin of the base, where the mean b/c ratio is 0.40 in D. basiovalis but only 0.25 in D. viirae sp. nov. (Fig. 5B). Moreover, D. viirae sp. nov. is characterised by a wider cusp when viewed from the side and, typically, a less developed carina on the cusp. The hypothesis that the D. viirae sp. nov. population is morphologically separate from the D. basiovalis population is supported by the PERMANOVA test (Fig. 5A), which shows that the probability that the two populations are the same is low (p (same) = 8.00E- 03). Drepanoistodus viirae sp. nov. is distinguished from the stratigraphically older Drepanoistodus contractus on the relatively wider and more compressed cusp and the usually less distinct longitudinal carina, and from D. cf. suberectus on the markedly smaller angle between the cusp and the upper margin of the base (mean angle = 46° in D. cf. suberectus, 30° in D. viirae sp. nov.). Occurrence The lower part of the L. variabilis Zone (sample LY12-13) to the lower part of the interzone (“uncertain interval”) between the L. variabilis Zone and the Y. crassus Zone (sample LY12-31) sensu Lindskog et al. (2020). In addition, D. viirae sp. nov. has been recorded from the B. norrlandicus and basal Y. crassus zones at Gillberga, Sweden (Löfgren 2000b, 2003); the uppermost part of the P. rectus – M. parva Zone at Steinsodden, Norway, which correlates with the uppermost P. originalis Zone (as D. cf. stougei sensu Rasmussen 2001); the lower part of the B. medius – H. holodentata Zone at Andersön, Sweden, correlating with the uppermost part of the L. variabilis Zone (as D. cf. basiovalis sensu Rasmussen 2001), and the L. variabilis Zone at Hällekis, Sweden (as D. aff. suberectus sensu Mellgren & Eriksson 2010). Moreover, it shares some characteristics with the geniculate element from strata correlated with the L. pseudoplanus Zone of the Canning Basin, Australia, which was included in D. basiovalis (Zhen 2020: fig. 7b), but this identification is questionable., Published as part of Rasmussen, Jan Audun, Eriksson, Mats E. & Lindskog, Anders, 2021, Middle Ordovician Drepanoistodus (Vertebrata, Conodonta) from Baltica, with description of three new species, pp. 106-134 in European Journal of Taxonomy 774 on pages 123-124, DOI: 10.5852/ejt.2021.774.1533, http://zenodo.org/record/5557148, {"references":["Sergeeva S. P. 1963. [Conodonts from the Lower Ordovician in the Leningrad region.] Paleontologicheshij Zhurnal 1963 (2): 93 - 108. [In Russian.]","Lofgren A. 2000 b. Early to early Middle Ordovician conodont biostratigraphy of the Gillberga quarry, northern Oland, Sweden. GFF 122: 321 - 338. https: // doi. org / 10.1080 / 11035890001224321","Lindskog A., Eriksson M. E., Rasmussen J. A., Dronov A. & Rasmussen C. M. O. 2020. Middle Ordovician carbonate facies development, conodont biostratigraphy and faunal diversity patterns at the Lynna River, northwestern Russia. Estonian Journal of Earth Sciences 69: 37 - 61. https: // doi. org / 10.3176 / earth. 2020.1.03","Rasmussen J. A. 2001. Conodont biostratigraphy and taxonomy of the Ordovician shelf margin deposits in the Scandinavian Caledonides. Fossils and Strata 48: 1 - 180.","Rasmussen J. A. 1991. Conodont stratigraphy of the Lower Ordovician Huk Formation at Slemmestad, southern Norway. Norsk Geologisk Tidsskrift 71: 265 - 88.","Branson E. B. & Mehl M. G. 1933. Conodont studies no. 2; conodonts from Joachim (Middle Ordovician) of Missouri; from the Plattin (Middle Ordovician) of Missouri; from the Maquoketa-Thebes (Upper Ordovician) of Missouri; a study of Hinde's types of conodonts preserved in the British Museum. Missouri University Studies 8: 77 - 167.","Feltes N. A. & Albanesi G. L. 2013. The Periodon and Paroistodus conodont biofacies in the lower member of the Las Aguaditas Formation (Middle Ordovician), Central Precordillera, Argentina. In: Albanesi G. L. & Ortega G. (eds) Conodonts from the Andes International Conodont Symposium: 17 - 23. Asociacion Paleontologica Argentina, Buenos Aires 3.","Zhen Y. Y. 2020. Revision of the Darriwilian (Middle Ordovician) conodonts documented by Watson (1988) from subsurface Canning Basin, Western Australia. Alcheringa 44: 217 - 252. https: // doi. org / 10.1080 / 03115518.2020.1737227","Lofgren A. 2003. Conodont faunas with Lenodus variabilis in the upper Arenigian to lower Llanvirnian of Sweden. Acta Palaeontologica Polonica 48: 417 - 436."]}
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- 2021
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27. Drepanoistodus Lindstrom 1971
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Rasmussen, Jan Audun, Eriksson, Mats E., and Lindskog, Anders
- Subjects
Conodonta ,Drepanoistodus ,Animalia ,Drepanoistodontidae ,Biodiversity ,Chordata ,Taxonomy ,Distacodontina - Abstract
Genus Drepanoistodus Lindström, 1971 Type species Oistodus forceps Lindström, 1955, subsequently designated by Lindström (1971). Remarks Drepanoistodus is here interpreted as quinquemembrate and comprises four nongeniculate coniform elements and one geniculate coniform element that collectively make a curvature-transition series from erect to recurved element types (e.g., Stouge & Bagnoli 1990; Rasmussen 1991). The nongeniculate elements comprise a suberectiform element associated with drepanodontiform type-l, type-2 and type-3 elements. In general, Middle Ordovician nongeniculate Drepanoistodus elements from Baltica can be described as follows: the suberectiform element is characterised by a straight, erect cusp. The drepanodontiform type-1 element has a strongly recurved cusp, which is keeled both anteriorly and posteriorly. The anterior keel is twisted strongly inwards. An extension, sometimes triangular in outline, may occur at the anterobasal corner. The drepanodontiform type-2 element has a recurved cusp which is keeled. It is separated from the drepanodontiform type-l element by the straight or only weakly twisted anterior margin, and by the consistent presence of an anterobasal flare, commonly with a triangular outline. The drepanodontiform type-3 element is typified by a slightly recurved cusp, which is anteriorly and posteriorly keeled and not twisted. As opposed to the drepanodontiform type-1 and type-2 elements, it lacks the anterior triangular flare. For a more comprehensive description, see Rasmussen (1991). Many coniform conodont apparatuses are not easily placed in the locational PMS notation scheme favoured by Sweet (1981, 1988), or the more biologically correct terminology advocated by Purnell et al. (2000), because it is very difficult or even impossible to identify locational homologues with the ozarkodinid notation (Smith et al. 2005). This is primarily a consequence of the lack of natural assemblages in many conodont genera and families, including Drepanoistodus. In most cases, it is extremely difficult to distinguish between individual Middle Ordovician Drepanoistodus species based on the largely homeomorphic nongeniculate elements (van Wamel 1974; Dzik 1983; Stouge 1984; Rasmussen 2001), and this is indeed also the case with respect to the species studied herein. Because our material includes nothing but isolated conodont elements (as opposed to articulated clusters or natural multi-element assemblages), the identification of Drepanoistodus at the species level is solely based on the geniculate element, which are described below. The stratigraphical distribution of the studied specimens of Drepanoistodus is shown in Table 3., Published as part of Rasmussen, Jan Audun, Eriksson, Mats E. & Lindskog, Anders, 2021, Middle Ordovician Drepanoistodus (Vertebrata, Conodonta) from Baltica, with description of three new species, pp. 106-134 in European Journal of Taxonomy 774 on pages 117-118, DOI: 10.5852/ejt.2021.774.1533, http://zenodo.org/record/5557148, {"references":["Lindstrom M. 1971. Lower Ordovician conodonts of Europe. Geological Society of America Memoirs 127: 21 - 61. https: // doi. org / 10.1130 / MEM 127 - p 21","Stouge S. & Bagnoli G. 1990. Lower Ordovician (Volkhovian - Kundan) conodonts from Hagudden, northern Oland, Sweden. Palaeontographica Italica 77: 1 - 54.","Rasmussen J. A. 1991. Conodont stratigraphy of the Lower Ordovician Huk Formation at Slemmestad, southern Norway. Norsk Geologisk Tidsskrift 71: 265 - 88.","Sweet W. C. 1981. Macromorphology of elements and apparatuses. In: Robison R. A. (ed.) Treatise on Invertebrate Paleontology, Part W, Miscellanea, Suppl. 2, Conodonta: 5 - 20. Geological Society of America and the University of Kansas Press, Lawrence.","Sweet W. C. 1988. The Conodonta: morphology, taxonomy, paleoecology, and evolutionary history of a long-extinct animal phylum. Oxford Monographs on Geology and Geophysics 10: 1 - 212.","Purnell M. A., Donoghue P. C. J. & Aldridge R. J. 2000. Orientation and anatomical notation in conodonts. Journal of Paleontology 74: 113 - 122. https: // doi. org / 10.1666 / 0022 - 3360 (2000) 074 2.0. CO; 2","Smith M. P., Donoghue P. C. J. & Repetski J. E. 2005. The apparatus composition and architecture of Cordylodus Pander - Concepts of homology in primitive conodonts. Bulletin of American Paleontology 369: 19 - 33.","Van Wamel W. A. 1974. Conodont biostratigraphy of the Upper Cambrian and Lower Ordovician of north-western bland, south-eastern Sweden. Utrecht Micropaleontological Bulletins 10: 1 - 126.","Dzik J. 1983. Early Ordovician conodonts from the Barrandian and Bohemian-Baltic faunal relationships. Acta Palaeontologica Polonica 28: 327 - 368.","Stouge S. 1984. Conodonts of the Middle Ordovician Table Head Formation, western Nemoundland. Fossils and Strata 16: 1 - 145.","Rasmussen J. A. 2001. Conodont biostratigraphy and taxonomy of the Ordovician shelf margin deposits in the Scandinavian Caledonides. Fossils and Strata 48: 1 - 180."]}
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- 2021
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28. Drepanoistodus suberectus
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Rasmussen, Jan Audun, Eriksson, Mats E., and Lindskog, Anders
- Subjects
Conodonta ,Drepanoistodus ,Animalia ,Drepanoistodontidae ,Biodiversity ,Chordata ,Drepanoistodus suberectus ,Taxonomy ,Distacodontina - Abstract
Drepanoistodus cf. suberectus (Branson & Mehl, 1933) Fig. 6T Drepanoistodus cf. suberectus (Branson & Mehl, 1933) – Löfgren 2003: fig. 7s–u. — Mellgren & Eriksson 2010: fig. 7k (only). — Hints et al. 2012: fig. 6h. Material examined Four geniculate elements including three from the Lynna section. Remarks Drepanoistodus cf. suberectus is included in the present work because it superficially resembles Drepanoistodus viirae sp. nov. Originally, D. suberectus was described as Oistodus suberectus from the Upper Ordovician strata of Missouri, USA, by Branson & Mehl (1933), but it was not until 1966 that conodont specialists included the geniculate element in the apparatus (see Bergström & Sweet 1966 and Webers 1966, for details). The D. suberectus type locality near Ozora, Missouri, was located and restudied by Bergström & Leslie (2010) who documented the conodont fauna and illustrated three different elements of D. suberectus, including the geniculate element. The Upper Ordovician geniculate D. suberectus elements (e.g., Stauffer 1935; Nowlan 2002; Bergström & Leslie 2010) are generally more rounded anteriorly and carry more pronounced keels on the cusp than the three geniculate elements at hand, thus leading us to leave the Lynna River specimens in open nomenclature. Drepanoistodus cf. suberectus occurs only sporadically in the Lynna River section samples. It is characterised by a short upper margin of the base compared to the free cusp (b/c ratio near 0.20 in the three specimens found). Angle A between the upper margin of the cusp and the carina on the cusp (see Fig. 3) varies considerably (41–52°) but it is wider than that of the other Drepanoistodus species described here. Moreover, it is typified by a convex basal margin; weakly rounded anterior margin, and a weakly developed carina on the straight cusp, which is located on the lower half part of the cusp. Superficially, D. cf. suberectus resembles D. viirae sp. nov. because of the relatively short base, but the latter species is distinguished by a narrower angle A (see Fig. 3); wider sides anteriorly on the cusp; laterally compressed cusp with distinct keels, and a median, as opposed to a lower, carina. Occurrence The Yangtzeplacognathus crassus Zone at Lynna River (samples LY12-34, LY14-2 and LY14-5). Drepanoistodus cf. suberectus has also been documented from the L. variabilis Zone of Hällekis, Sweden (Mellgren & Eriksson 2010)., Published as part of Rasmussen, Jan Audun, Eriksson, Mats E. & Lindskog, Anders, 2021, Middle Ordovician Drepanoistodus (Vertebrata, Conodonta) from Baltica, with description of three new species, pp. 106-134 in European Journal of Taxonomy 774 on page 127, DOI: 10.5852/ejt.2021.774.1533, http://zenodo.org/record/5557148, {"references":["Branson E. B. & Mehl M. G. 1933. Conodont studies no. 2; conodonts from Joachim (Middle Ordovician) of Missouri; from the Plattin (Middle Ordovician) of Missouri; from the Maquoketa-Thebes (Upper Ordovician) of Missouri; a study of Hinde's types of conodonts preserved in the British Museum. Missouri University Studies 8: 77 - 167.","Lofgren A. 2003. Conodont faunas with Lenodus variabilis in the upper Arenigian to lower Llanvirnian of Sweden. Acta Palaeontologica Polonica 48: 417 - 436.","Hints O., Viira V. & Nolvak J. 2012. Darriwilian (Middle Ordovician) conodont biostratigraphy in NW Estonia. Estonian Journal of Earth Sciences 61: 210 - 226. https: // doi. org / 10.3176 / earth. 2012.4.03","Bergstrom S. M. & Sweet W. C. 1966. Conodonts from the Lexington Limestone (Middle Ordovician) of Kentucky and its lateral equivalents in Ohio and Indiana. Bulletin of American Paleontology 50: 269 - 441.","Webers G. F. 1966. The Middle and Upper Ordovician Conodont Faunas of Minnesota. Minnesota Geological Survey, Special Publication 4: 1 - 123.","Bergstrom S. M. & Leslie S. A. 2010. The Ordovician zone index conodont Amorphognathus ordovicicus Branson & Mehl, 1933 from its type locality and the evolution of the genus Amorphognathus Branson & Mehl, 1933. Journal of Paleontology 29: 73 - 80. https: // doi. org / 10.1144 / jm. 29.1.73","Stauffer C. R. 1935. Conodonts of the Glenwood beds. Geological Society of America Bulletin 46: 125 - 168. https: // doi. org / 10.1130 / GSAB- 46 - 125","Nowlan G. S. 2002. Stratigraphy and conodont biostratigraphy of Upper Ordovician strata in the subsurface of Alberta, Canada. Special Papers in Palaeontology 67: 185 - 203."]}
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- 2021
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29. Drepanoistodus iommii Rasmussen & Eriksson & Lindskog 2021, sp. nov
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Rasmussen, Jan Audun, Eriksson, Mats E., and Lindskog, Anders
- Subjects
Conodonta ,Drepanoistodus ,Drepanoistodus iommii ,Animalia ,Drepanoistodontidae ,Biodiversity ,Chordata ,Taxonomy ,Distacodontina - Abstract
Drepanoistodus iommii sp. nov. urn:lsid:zoobank.org:act: 0E2832F5-672E-4FAE-B5A5-CBA5DE1A4824 Fig. 6E–H partim Drepanoistodus aff. basiovalis – Mellgren & Eriksson 2010: fig. 7m (only). Drepanoistodus cf. basiovalis – Mellgren et al. 2012: fig. 5e. Diagnosis A Drepanoistodus species characterised by a geniculate element with distinct keels on the cusp and upper margin of the base; a straight basal margin; a straight to weakly rounded (convex) anterior margin and cusp which is approximately twice the length of the upper margin of the base. Etymology Named in honour of legendary guitarist Tony Iommi, founding member of heavy metal band Black Sabbath. Material examined Ten geniculate elements including eight from the Lynna section. Holotype, geniculate element (Fig. 6E–F); LO 12479T. Type locality River bank near the mouth of Lynna River, village of Kolchanovo, St. Petersburg region, Russia (60°00′39″ N, 32°33′49″ E). Type stratum Approximately 10 cm above the local base of the Lynna Formation, sample LY 12-16. Lower part of the Lenodus variabilis Zone. Description Cusp reclined and straight with distinct keels developed on the anterior (upper) and posterior (lower) margins. A median, longitudinal carina is developed on both sides of the cusp, but it is especially distinct on the inner side. Base is characterised by a straight or almost straight basal margin and a distinct keel on the upper margin. Whereas this keel is slightly convex, the upper margin below the keel is straight. Anterior margin is usually straight or weakly rounded (convex), but occasionally, it is strongly rounded. Angle A between the cusp and upper margin of the base is ca 30° (mean) with a standard deviation at 4.2 (Fig. 5B), and the mean ratio between length of the free upper margin (b) and the free cusp (c) is 0.54 (standard deviation 0.10). Remarks In the PCA plot (Fig. 4), the population of D. iommii sp. nov. is situated in the upper right corner, separated from the D. basiovalis population as well as the other two new species populations described herein. The vectors in the biplot demonstrate that this is mainly due to the straight basal margin, the relatively long upper margin (high b/c values), and the usually straight anterior margin in D. iommii sp. nov., which is in accordance with the characters diagnosed above. The hypothesis that the population of D. iommii sp. nov. is morphologically different from the D. basiovalis population is supported by the PERMANOVA test (Fig. 5A), which shows that the probability that the two populations are the same is exceedingly low (p (same) = 1.00E- 04). Occurrence The L. antivariabilis Zone (sample LY12-9) to the L. variabilis Zone (sample LY12-21b). Outside the St. Petersburg region, D. iommii sp. nov. has been recorded from the L. variabilis Zone at the Hällekis quarry in Västergötland, Sweden (Mellgren & Eriksson 2010; referred to as D. aff. basiovalis) and from the L. pseudoplanus Zone or E. suecicus Zone of the island Osmussaar, Estonia (Mellgren et al. 2012; reported as D. cf. basiovalis)., Published as part of Rasmussen, Jan Audun, Eriksson, Mats E. & Lindskog, Anders, 2021, Middle Ordovician Drepanoistodus (Vertebrata, Conodonta) from Baltica, with description of three new species, pp. 106-134 in European Journal of Taxonomy 774 on pages 119-120, DOI: 10.5852/ejt.2021.774.1533, http://zenodo.org/record/5557148, {"references":["Mellgren J. I. S., Schmitz B., Ainsaar L., Kirsimae K. & Eriksson M. E. 2012. Conodont dating of the Middle Ordovician breccia cap-rock limestone on Osmussaar Island, northwestern Estonia. Estonian Journal of Earth Sciences 61: 133 - 148. https: // doi. org / 10.3176 / earth. 2012.3.01"]}
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- 2021
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30. Drepanoistodus basiovalis
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Rasmussen, Jan Audun, Eriksson, Mats E., and Lindskog, Anders
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Conodonta ,Drepanoistodus ,Animalia ,Drepanoistodontidae ,Biodiversity ,Chordata ,Drepanoistodus basiovalis ,Taxonomy ,Distacodontina - Abstract
Drepanoistodus basiovalis (Sergeeva, 1963) Fig. 6A–D Oistodus basiovalis Sergeeva, 1963: 96, pl. 7 figs 6–7, text-fig. 3. Drepanoistodus basiovalis – Lindström 1971: 43, text-figs 6, 8. — Stouge & Bagnoli 1990: 15, pl. 5 figs 18–24. — Dzik 1990: fig. 12; 1994: 78, pl. 16 figs. 16–20, text-fig. 12a; 2020: fig. 7A–E. — Rasmussen 1991: 277, fig. 6l; 2001: 71–73, pl. 5: 9 (cum. syn.). — Löfgren 1994: fig. 6.30; 2000a: fig. 4w; 2006: figs 3n, 3ab. — Viira et al. 2001: fig. 5z. — Zhen & Percival 2004: 93, fig. 11a–j. — Tolmacheva et al. 2013: pl. 3, fig. 24. partim Drepanoistodus basiovalis – Löfgren 1978: 55–56, pl. 1 figs 11–16 (only), non 17 (= D. contractus (Lindström, 1955)). — Olgun 1987: 49, pl. 6w (only). — Landing et al. 2003: fig. 4e (only). — Zhen et al. 2011: 222–227, fig. 12a?, b–n, p–q (only). cf. Drepanoistodus basiovalis – Zhang 1998: 61–62, pl. 5 figs 5–12 (unusually short upper margin of the base). ? Drepanoistodus basiovalis – Lehnert et al. 1998: 55, pl. 3 figs 6, 12 (12 may belong to Paroistodus originalis (Sergeeva, 1963)). — Boncheva et al. 2009: text-fig. 3.8 (broken element). — Albanesi & Ortega 2016: fig. 7(6) (shares characters with D. basiovalis and D. cf. balticus). — Feltes et al. 2016: fig. 3ac. — Wu et al. 2018: fig. 5e (unusually long base compared to the cusp). non Drepanoistodus basiovalis – Gutiérrez-Marco et al. 2008: 153, figs 3.29–3.31 (may be Drepanoistodus cf. basiovalis or Drepanoistodus cf. suberectus (Branson & Mehl, 1933). — Hints et al. 2012: fig. 6h (= Drepanoistodus cf. suberectus). — Wu et al. 2017: fig. 7u (= Drepanoistodus contractus (Lindström)). — Lindskog et al. 2020: fig. 7v–w (= Drepanoistodus viirae sp. nov.). Original diagnosis (translated from Sergeeva, 1963 [in Russian]) Inclined conodonts, almost symmetrical, with a wide shortened base, the edge of which is rounded. Material examined 33 geniculate elements including 24 from the Lynna section. Original description, slightly shortened (translated from Sergeeva, 1963 [in Russian]) Medium-sized conodonts (0.52–0.92 mm), inclined; the degree of inclination of the cusp is 45–60°, sometimes up to 80°. Base high, not very long, elongated along the CD; base length 2.5–3 times its height (comment by the authors: “ we find the meaning of the latter measure ambiguous ”). Base wall slightly transparent near the edge, rounded. The angle between the sides AC is more than 90°; angle between AD 40–45°; corners are smoothly obtuse. Transverse in cross section, the base is oval, elongated along CD and compressed along L1L2. From the C side, the base is compressed, sometimes with a thin keel near the tip, with a small keel on side D. The sides of the base L1 and L2 are smooth and flat. Basal cavity is not always visible, it is wide, but not deep, without visible tops. The cusp is long, straight or slightly curved towards L1, sharply tapering towards the tip; compressed. The sides of the cusp are almost flat, with a welldeveloped longitudinal, wide carina on L1 and less developed carina on the side L2. The carinae usually run from the base to the tip of the cusp. Thin keels occur on the lower (D) and upper (C) parts of the cusp. Remarks In her original diagnosis, Sergeeva (1963) only included geniculate elements with a rounded basal margin in “ Oistodus ” basiovalis, which is also evident from the species epithet: basiovalis (meaning oval base). This interpretation of the geniculate element in Drepanoistodus basiovalis is followed here. Additional typical characters that may be added to the original species description include: anterior margin and upper anterior corner rounded or weakly rounded; cusp usually straight; a median or median to lower, longitudinal carina present on the inner (sometimes slightly concave) side of the element. Carina is more distinct in Darriwilian specimens than in Dapingian ones. Whereas angle A (Fig. 3) between the cusp and the upper margin is 29.6° with a standard deviation at 5.6, the mean ratio between the length of the free upper margin and free cusp (b/c ratio) reaches 0.40 with a standard deviation of 0.1 (Fig. 5B). Occurrence Drepanoistodus basiovalis occurs from the L. antivariabilis Zone (sample LY12-9) to the interzone (“uncertain interval”) between the L. variabilis Zone and the Y. crassus Zone sensu Lindskog et al. (2020) in the Lynna River section (sample LY12-21b; between LY12-21 and LY12-22). In addition, D. basiovalis has been reported from several other localities in Baltoscandia and Poland, and also outside the Baltica palaeocontinent, e.g., New Brunswick, Argentina, Australia and China (for references, see the synonymy list above)., Published as part of Rasmussen, Jan Audun, Eriksson, Mats E. & Lindskog, Anders, 2021, Middle Ordovician Drepanoistodus (Vertebrata, Conodonta) from Baltica, with description of three new species, pp. 106-134 in European Journal of Taxonomy 774 on pages 118-119, DOI: 10.5852/ejt.2021.774.1533, http://zenodo.org/record/5557148, {"references":["Sergeeva S. P. 1963. [Conodonts from the Lower Ordovician in the Leningrad region.] Paleontologicheshij Zhurnal 1963 (2): 93 - 108. [In Russian.]","Lindstrom M. 1971. Lower Ordovician conodonts of Europe. Geological Society of America Memoirs 127: 21 - 61. https: // doi. org / 10.1130 / MEM 127 - p 21","Stouge S. & Bagnoli G. 1990. Lower Ordovician (Volkhovian - Kundan) conodonts from Hagudden, northern Oland, Sweden. Palaeontographica Italica 77: 1 - 54.","Dzik J. 1990. Conodont evolution in high latitudes of the Ordovician. Courier Forschungsinstitut Senckenberg 117: l - 28.","Rasmussen J. A. 1991. Conodont stratigraphy of the Lower Ordovician Huk Formation at Slemmestad, southern Norway. Norsk Geologisk Tidsskrift 71: 265 - 88.","Lofgren A. 1994. Arenig (Lower Ordovician) conodonts and biozonation in the eastern Siljan district, central Sweden. Journal of Paleontology 68: 1350 - 1368. https: // doi. org / 10.1017 / S 0022336000034338","Viira V., Lofgren A., Magi S. & Wickstrom J. 2001. An Early to Middle Ordovician succession of conodont faunas at Maekalda, northern Estonia. Geological Magazine 138: 699 - 718. https: // doi. org / 10.1017 / S 0016756801005945","Zhen Y. Y. & Percival I. G. 2004. Middle Ordovician (Darriwilian) conodonts from allochthonous limestones in the Oakdale Formation of central New South Wales. Alcheringa 28: 77 - 111. https: // doi. org / 10.1080 / 03115510408619276","Tolmacheva T. Yu., Zaitsev A. V. & Alekseev A. S. 2013. Middle and Upper Ordovician conodonts of the Moscow Syneclise: new data on stratigraphy of the borehole Gavrilov Yam- 1 section. Stratigrafiya. Geologicheskaya Korrelyatsiya 21: 52 - 77. https: // doi. org / 10.1134 / S 0869593813040096","Lofgren A. 1978. Arenigian and Llanvirnian conodonts from Jamtland, northern Sweden. Fossils and Strata 13: 1 - 129.","Olgun O. 1987. Komponenten-Analyse und Conodonten-Stratigraphie der Orthoceratenkalksteine im Gebiet Falbygden, Vastergotland, Mittelschweden. Sveriges Geologiska Undersokning, Ser. Ca 70: 1 - 78.","Landing E., Westrop S. R. & Kim D. H. 2003. First Middle Ordovician biota from southern New Brunswick: stratigraphic and tectonic implications for the evolution of the Avalon continent. Canadian Journal of Earth Sciences 40: 715 - 730. https: // doi. org / 10.1139 / E 03 - 009","Zhen Y. Y., Wang Z. H., Zhang Y. D., Bergstrom S. M., Percival I. G. & Chen J. F. 2011. Middle to Late Ordovician (Darriwilian - Sandbian) conodonts from the Dawangou Section, Kalpin area of the Tarim Basin, northwestern China. Records of the Australian Museum 63: 203 - 266. https: // doi. org / 10.3853 / j. 0067 - 1975.63.2011.1586","Zhang J. 1998. Conodonts from the Guniutan Formation (Llanvirnian) in Hubei and Hunan Provinces, south-central China. Stockholm Contributions in Geology 46: 1 - 161.","Lehnert D., Keller M. & Bordonaro D. 1998. Early Ordovician conodonts from the southern Cuyania terrane (Mendoza Province, Argentina). In: H. Szaniawski (ed.) Proceedings of the Sixth European Conodont Symposium (ECOS VI). Palaeontologia Polonica 58: 47 - 65.","Boncheva I., Goncuoglu M. C., Leslie S. A., Lakova I., Sachanski V., Saydam G., Gedik I. & Koenigshof P. 2009. New conodont and palynological data from the Lower Palaeozoic in Northern Camdag, NW Anatolia, Turkey. Acta Geologica Polonica 59: 157 - 171.","Albanesi G. L. & Ortega G. 2016. Conodont and graptolite biostratigraphy of the Ordovician System of Argentina. In: Montenari M. (ed.) Stratigraphy and Timescales 1: 61 - 121. https: // doi. org / 10.1016 / bs. sats. 2016.10.002","Feltes N. A., Albanesi G. L. & Bergstrom S. M. 2016. Conodont biostratigraphy and global correlation of the Middle Darriwilian - Lower Sandbian Las Aguaditas Formation, Precordillera of San Juan, Argentina. Andean Geology 43: 60 - 85. https: // doi. org / 10.5027 / andgeoV 43 n 1 - a 04","Wu R. - C., Calner M., Lehnert O., Lindskog A. & Joachimski M. 2018. Conodont biostratigraphy and carbon isotope stratigraphy of the Middle Ordovician (Darriwilian) Komstad Limestone, southern Sweden. GFF 140: 44 - 54. https: // doi. org / 10.1080 / 11035897.2018.1435561","Gutierrez-Marco J. C., Albanesi G. L., Sarmiento G. N. & Carlotto V. 2008. An Early Ordovician (Floian) Conodont Fauna from the Eastern Cordillera of Peru (Central Andean Basin). Geologica Acta 6: 147 - 160.","Branson E. B. & Mehl M. G. 1933. Conodont studies no. 2; conodonts from Joachim (Middle Ordovician) of Missouri; from the Plattin (Middle Ordovician) of Missouri; from the Maquoketa-Thebes (Upper Ordovician) of Missouri; a study of Hinde's types of conodonts preserved in the British Museum. Missouri University Studies 8: 77 - 167.","Hints O., Viira V. & Nolvak J. 2012. Darriwilian (Middle Ordovician) conodont biostratigraphy in NW Estonia. Estonian Journal of Earth Sciences 61: 210 - 226. https: // doi. org / 10.3176 / earth. 2012.4.03","Wu R. - C., Calner M. & Lehnert O. 2017. Integrated conodont biostratigraphy and carbon isotope chemostratigraphy in the Lower-Middle Ordovician of southern Sweden reveals a complete record of the MDICE. Geological Magazine 154: 334 - 353. https: // doi. org / 10.1017 / S 0016756816000017","Lindskog A., Eriksson M. E., Rasmussen J. A., Dronov A. & Rasmussen C. M. O. 2020. Middle Ordovician carbonate facies development, conodont biostratigraphy and faunal diversity patterns at the Lynna River, northwestern Russia. Estonian Journal of Earth Sciences 69: 37 - 61. https: // doi. org / 10.3176 / earth. 2020.1.03"]}
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- 2021
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31. Kovács Sándor conodonta-gyűjteménye.
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Viktor, Karádi and Alfréd, Dulai
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The collection of the Department of Palaeontology and Geology of the Hungarian Natural History Museum was enriched by a microfossil material which is scientifically greatly important and unique in Hungary. In 2010, when Sándor Kovács passed away, his conodont collection was moved to the Department of Palaeontology of the Eötvös Loránd University. Following years of classification and partly processing, the material was donated to the museum. Conodonts are known from marine beds of the Palaeozoic and the Triassic and they are highly significant from the stratigraphical point of view. Due to their rapid evolution, conodont elements are used worldwide for correlating different successions, despite their uncertain systematic affinities. Beside conodonts, other microfossil groups can also be found in the collection that contains thousands of fossils. The material is mostly from Hungary, but localities from other countries are represented as well. [ABSTRACT FROM AUTHOR]
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- 2016
32. A new early Silurian prioniodontid conodont with three P elements from Iran and associated species.
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MÄNNIK, PEEP, MILLER, C. GILES, and HAIRAPETIAN, VACHIK
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CONODONTS , *LLANDOVERY series , *SILURIAN Period , *BRACHIOPODA - Abstract
A prioniodontid conodont Arianagnathus jafariani gen. et sp. nov. from the late Llandovery part of the Niur Formation of the Derenjal Mountains, East Central Iran had an apparatus bearing 3 pairs of P elements. Pa elements of its apparatus are closest to those of Icriodella sandersi (Llandovery-Wenlock boundary interval, Wales, Great Britain) in the weak development of an icrion. Due to the small sample size not all S-elements have been identified but those present are similar to those described in the Icriodella and Icriognathus apparatuses. Based on similarities with previously described apparatus Notiodella we suggest that Arianagnathus jafariani gen. et sp. nov. probably had an apparatus of 17 elements. Arianagnathus is therefore an important additional example that has potential for aiding the future revision of the palaeobiological arrangement of elements within and the phylogeny of conodont apparatuses with 3 P elements, one of which is icrion bearing. The completely known apparatus of associated Ozarkodina derenjalensis sp. nov. shows similarity to some unnamed Ozarkodina from Wales, Great Britain. Many of the conodonts found in the Llandovery part of the studied section are cosmopolitan; the new conodont species seem to have their possible closest relatives in Avalonia. [ABSTRACT FROM AUTHOR]
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- 2015
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33. Taxonomy and evolution of the Triassic conodont Pseudofurnishius.
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PLASENCIA, PABLO, HIRSCH, FRANCIS, JINGENG SHA, and MÁRQUEZ-ALIAGA, ANA
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TRIASSIC paleontology , *CONODONTS , *FOSSIL animals , *TRIASSIC Period , *BIOLOGICAL classification - Abstract
Pseudofurnishius is a late Anisian (Pelsonian)--early Carnian (Cordevolian) conodont genus of gondolellid stock, characteristic for the Sephardic Province and restricted to the "Southern Tethys" region of the northern margin of Gondwana. Its most commonly found species, Pseudofurnishius murcianus, appears at the base of the Ladinian (Fassanian). The Ladinian material of Spain reveals its ontogeny characterised by initial lateral protrusions from the carina that may develop first mono-platform and later bi-platform units, finally evolving into elaborated multi-denticulated forms. The late Anisian-- early Carnian phylogenesis of Pseudofurnishius priscus → P. shagami → P. murcianus is proposed. At the end of the Ladinian, Pseudofurnishius expanded to the entire "Southern Tethys" shelf and into Cimmerian terranes that drifted away from northern Gondwana, now accreted to Eurasia, such as the Sibumasu terrane (Southwest China--Malayan Peninsula). [ABSTRACT FROM AUTHOR]
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- 2015
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34. New group of the Early Palaeozoic conodont-like fossils.
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Szaniawski, Hubert
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FOSSIL microorganisms , *CONODONTS , *FOSSILS , *CAMBRIAN Period ,CAMBRIAN stratigraphic geology - Abstract
The paper is devoted to the Upper Cambrian and Tremadocian organophosphatic microfossils which were hitherto treated as conodonts and assigned mainly to the genera Coelocerodontus and Viirodus. Individual elements of the fossils, similarly to the elements of conodonts, belonged originally to the multi-element apparatuses. Present studies, based mainly on the collections from Sweden, Poland (core sections), Estonia and Kazakhstan, show that despite the similarities of their individual elements to conodonts, they significantly differ from them in the inner structure, as well as in the construction of the apparatuses composed of them. Elements of their apparatuses are matched in shape to each other and certainly functioned in conjunction, while those belonging to the euconodont apparatuses are usually differentiated in shape and usually functioned in separation. All fossils of this group are provisionally named coelocerodonts in this paper. Their individual elements, as well as the apparatuses composed of them, are similar in construction to those of the genus Phakelodus, which is an ancestor of chaetognaths. [ABSTRACT FROM AUTHOR]
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- 2015
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35. Middle Ordovician Drepanoistodus (Vertebrata, Conodonta) from Baltica, with description of three new species
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Jan Audun Rasmussen, Mats Eriksson, and Anders Lindskog
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Range (biology) ,Zoology ,Biology ,Baltica ,Conodonta ,Sensu ,ddc:590 ,Conodont ,Animalia ,Chordata ,Open nomenclature ,Ecology, Evolution, Behavior and Systematics ,conodont ,Taxonomy ,new species ,Drepanoistodus ,Holotype ,Botany ,Ordovician ,Biodiversity ,biology.organism_classification ,New species ,Taxon ,QL1-991 ,QK1-989 ,Drepanoistodontidae ,Distacodontina - Abstract
Drepanoistodus basiovalis (Sergeeva, 1963) is a common conodont species in Middle Ordovician strata of Baltica. For many years it has been widely accepted that the species encompasses a wide range of morphological plasticity. Hence, several different morphotypes that significantly deviate from the holotype have nonetheless been included in the broad species concept. In this study, we performed a detailed taxonomical study on 112 predominantly well-preserved specimens (geniculate elements) from the St. Petersburg region of Russia; 37 of these were selected for morphometric analyses together with 21 well-illustrated specimens from the published literature. The results demonstrate that, among the morphotypes that share some characteristics with D. basiovalis sensu lato, at least five species can be readily distinguished. Hence, three new species – Drepanoistodus iommii sp. nov., D. svendi sp. nov. and D. viirae sp. nov. – are here added to the previously known D. basiovalis and D. contractus (Lindström, 1955). In addition, some specimens were left under open nomenclature and assigned to Drepanoistodus aff. basiovalis and D. cf. suberectus (Branson & Mehl, 1933). In order to objectively compare the Drepanoistodus taxa and test the validity of the new species, we performed a Principal Component Analysis combined with non-parametric (PERMANOVA) tests based on 21 morphological characters.
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- 2021
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36. Global climate changes account for the main trends of conodont diversity but not for their final demise
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Nicolas Goudemand, Samuel Ginot, Laboratoire d'Ecologie des Hydrosystèmes Naturels et Anthropisés (LEHNA), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-École Nationale des Travaux Publics de l'État (ENTPE)-Centre National de la Recherche Scientifique (CNRS), Inflammasome NLRP3 – NLRP3 Inflammasome, Centre International de Recherche en Infectiologie - UMR (CIRI), Institut National de la Santé et de la Recherche Médicale (INSERM)-École normale supérieure - Lyon (ENS Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-École normale supérieure - Lyon (ENS Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS), ANR-14-ACHN-0010,EvoDevOdonto,Origine et evolution des appendices epitheliaux chez les vertebres: une perspective interdisciplinaire(2014), Centre International de Recherche en Infectiologie (CIRI), École normale supérieure de Lyon (ENS de Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure de Lyon (ENS de Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), CCSD, Accord Elsevier, Accueil de Chercheurs de Haut Niveau - Origine et evolution des appendices epitheliaux chez les vertebres: une perspective interdisciplinaire - - EvoDevOdonto2014 - ANR-14-ACHN-0010 - @RAction - VALID, École normale supérieure - Lyon (ENS Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure - Lyon (ENS Lyon)-Université Claude Bernard Lyon 1 (UCBL), and Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
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010504 meteorology & atmospheric sciences ,Permian ,Paleobiology Database ,Early Triassic ,02 engineering and technology ,Oceanography ,Marine regression ,01 natural sciences ,Mass extinction ,Paleontology ,Conodonta ,0202 electrical engineering, electronic engineering, information engineering ,14. Life underwater ,Sea level ,0105 earth and related environmental sciences ,Extinction event ,Global and Planetary Change ,biology ,Court Jester ,020206 networking & telecommunications ,biology.organism_classification ,Abiotic drivers ,[SDE.BE] Environmental Sciences/Biodiversity and Ecology ,Past climate ,Past climate Court Jester Abiotic drivers Conodonta Mass extinction ,13. Climate action ,Ordovician ,[SDE.BE]Environmental Sciences/Biodiversity and Ecology ,Conodont ,Geology - Abstract
International audience; Conodonts, one of the longest-lived early groups of vertebrates, have a very complete fossil record ranging from the late Cambrian to the end of the Triassic and persisted through many global climatic and biotic events. In this paper, we analyse a large dataset harvested from the Paleobiology Database to compute global diversity curves at the generic level and explore patterns of conodont paleogeographic distribution. Our results partly confirm the most prominent findings of earlier studies including the occurrence of an Ordovician acme, a Permian nadir and a short-lived Triassic recovery. Major peaks of origination were found in the Early Ordovician and Early Triassic, while major extinctions occurred in the Upper Ordovician and Pennsylvanian. Paleogeographical extent of conodonts was impacted by i) the position of paleo-continents (notably impacting the latitudinal gradient of diversity), ii) the available continental shelf area and iii) ice sheets expansion. Diversity trends were mostly impacted by transitions between hothouse and icehouse ages, with major glaciations and associated marine regressions co-occurring with major extinctions. The influence of global sea level was less marked than that of temperature. However, the final demise of conodonts at the end of the Triassic did not coincide with either a major glaciation or marine regression. This supports the view that extinction of the group was mostly due to biotic factors such as competition with ‘Mesozoic’ taxa.
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- 2020
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37. Upper Furongian (Cambrian) conodonts from the Degerhamn quarry road section, southern Öland, Sweden.
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Bagnoli, Gabriella and Stouge, Svend
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CONODONTS , *CAMBRIAN explosion (Evolution) , *SHALE , *GEOLOGICAL formations , *STRATIGRAPHIC geology - Abstract
The Alum Shale Formation exposed at the Degerhamn quarry road section, southern Öland, Sweden, contains a diversified assemblage of euconodonts, paraconodonts and protoconodonts, the majority of which have ranges confined to the Furongian Series (Cambrian). The first occurrence (FO) of the cosmopolitan euconodont speciesProconodontus muelleriis recorded in the uppermost part of theCtenopyge spectabilistrilobite Zone and the first appearance datum ofCordylodus?andresiis in the upper part of theParabolina lobatatrilobite Zone. Three new successive paraconodont associations are introduced: (1) theFurnishinaAssociation, (2) theProoneotodusAssociation and (3) theWestergaardodinaAssociation, which, respectively, correspond to deeper marine, deep marine and shallow marine conditions. The genusStenodontusChen & Gong is revised in multielement taxonomy. New species formally named areFurnishina holmiandWestergaardodina asinina;Furnishinasp. A andFurnishinasp. B are described in open nomenclature. [ABSTRACT FROM AUTHOR]
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- 2014
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38. UPPER DEVONIAN CONODONTS FROM LADAKH, HIMALAYA, INDIA
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GUPTA, V. J. and UPPAL, S.
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lcsh:Geology ,lcsh:Paleontology ,lcsh:QE1-996.5 ,Conodonta ,Biostratigraphy ,Chronostratigraphy ,Devonian ,Himalaya ,lcsh:QE701-760 - Abstract
The preserit paper describes Upper Devonian conodont fauna from the black and bluish limestone succession lying immediately above the Muth Quartzite exposed near the village Tanze, Luneak valley, Ladakh.
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- 2020
39. PERMIAN-TRIASSIC BOUNDARY AND EARLY TRIASSIC CONODONTS FROM THE SOUTHERN ALPS, ITALY
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PERRI, MARIA CRISTINA and ANDRAGHETTI, MIRELLA
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lcsh:Geology ,Conodonta ,Taxonomy ,Biostratigraphy ,Permian/Triassic ,Southern Alps ,Italy ,lcsh:Paleontology ,lcsh:QE1-996.5 ,lcsh:QE701-760 - Abstract
The Bellerophon (Late Permian) and Werfen (Lower Triassic) Formations were investigated on the basis of conodonts. Fifteen sections were sampled from Carnic Alps and Dolomites area in the Southern Alps. Ten were productive. The Bellerophon Formation yielded a few specimens of Hindeodus typicalis, Ellisonia agordina and Ellisonia sp. In the Werfen Formation were collected Hindeodus typicalis, Ellisonia agordina, E. triassica, Hadrodontina anceps, Xaniognathus gradatus, Isarcicella isarcica, Pachycladina obliqua, Ellisonia delicatula, Neospathodus triangularis. In describing the conodont fauna, multielement taxonomy is applied. Ellisonia agordina is a new species found at the top of the Bellerophon Formation and from the Tesero to the Siusi Members of the Werfen Formation, i, e. at the Permian — Triassic boundary and in the Lower Triassic. The apparatus of this new species is described. In the Southern Alps the range of Hindeodus typicalis, previously known in the Werfen Formation, extends down into the uppermost Bellerophon Formation. All species confirm the ranges found elsewhere in the world. On the basis of only the conodont fauna, it is not possible as yet to recognize the position of the Permian — Triassic boundary more precisely in the Bellerophon/Werfen Formations in the Southern Alps. It is obvious, however, that the recovery of Isarcicella isarcica allows the certain identification of the Triassic.
- Published
- 2020
40. Faunal dynamics across the Silurian-Devonian positive isotope excursions (δ13C, δ18O) in Podolia, Ukraine: Comparative analysis of the Ireviken and Klonk events.
- Author
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RACKI, GRZEGORZ, BALIŃSKI, ANDRZEJ, WRONA, RYSZARD, MAŁKOWSKI, KRZYSZTOF, DRYGANT, DANIEL, and SZANIAWSKI, HUBERT
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DEVONIAN Period , *CARBONATES , *BIOTIC communities , *ECOLOGICAL research - Abstract
Two global isotopic events, the early Sheinwoodian (early Wenlock) and that at the Silurian-Devonian transition, have been comprehensively studied in representative carbonate successions at Kytayhorod and Dnistrove, respectively, in Podolia, Ukraine, to compare geochemistry and biotic changes related correspondingly to the Ireviken and Klonk events. These two large-scale isotope excursions reveal different regional ecosystem tendencies. The well-defined increasing trend across the Llandovery-Wenlock boundary in siliciclastic input, redox states and, supposedly, bioproductivity, was without strict correlative relations to the major 13C enrichment event. The environmental and biotic evolution was forced by eustatic sea-level fluctuations and two-step climate change toward a glaciation episode, but strongly modified by regional epeirogeny movements due to location near the mobile Teisseyre-Törnquist Fault Zone. Thus, the global early Sheinwoodian biogeochemical perturbation was of minor depositional significance in this epeiric sea, as in many other Laurussian domains. Conversely, the Podolian sedimentary record of the Klonk Event exhibits temporal links to the abrupt δ13C anomaly, overprinted by a tectonically driven deepening pulse in the crucial S-D boundary interval. This carbon cycling turnover was reflected in the regional carbonate crisis and cooling episodes, paired with a tendency towards eutrophication and recurrent oxygen deficiency, but also with major storms and possible upwelling. Faunal responses in both Podolian sections follow some characters of the Silurian pattern worldwide, as manifested by conodont changeover prior to the major early Sheinwoodian isotopic/climatic anomaly. This contrasts with the relative brachiopod and chitinozoan resistances in the course of the Ireviken Event. Also, during the Klonk Event, a moderate faunal turnover, both in benthic and pelagic groups, occurred only near the very beginning of the prolonged 13C-enriched timespan across the system boundary, possibly due to progressive dysoxia and temperature drop. The characters point to a peculiarity of the Klonk Event by comparison with the Silurian global events, and some similarity already to the succeeding Devonian transgressive/anoxic episodes. [ABSTRACT FROM AUTHOR]
- Published
- 2012
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41. Lochkovian conodonts from Podolia, Ukraine, and their stratigraphic significance.
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DRYGANT, DANIEL and SZANIAWSKI, HUBERT
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GEOLOGICAL basins , *CARBONATES , *CONODONTS - Abstract
In the Podolian Dniester Basin (southwestern Ukraine) the Lower Devonian marine deposits are represented by about 530 m thick continuous sequence of interlaminated carbonate and schale outcrops at several localities. Conodonts occur in most of the carbonate layers of the whole Lochkovian but are not abundant and their ramiform elements are mostly broken or lacking. Therefore, only the pectiniform, Pa elements of twenty five stratigraphically important conodont species occurring in the region are discussed and two new species, Caudicriodus schoenlaubi and Pandorinellina? parva are proposed. The hypothetical phyletic relationships within the main representatives of the icriodontid and spathognathodontid genera, Caudicriodus, Zieglerodina, and Pandorinellina? are traced. Comparison of the previously published and newly obtained data revealed discrepancies in the hitherto used interpretation of some of the conodont taxa and their stratigraphic ranges. Contrary to the earlier reports, Caudicriodus postwoschmidti does not occur in the lower Lochkovian but only in the middle part of the Chortkiv Formation, high above the Monograptus uniformis Zone. Based on new material and verification of the previous determinations, a modified scheme of the Lochkovian conodont zonation in Podolia is proposed. Conodont zones: Caudicriodus hesperius, C. transiens, C. postwoschmidti, C. serus, and ?Caudicriodus steinachensis are distinguished. The zones are correlated with conodont zonations in other regions--Barrandian, Cantabrian Mountains, Pyrenees, and Nevada. Biostratigraphy of the Siluro-Devonian transition and Lochkovian is integrated with the carbon isotope stratigraphy. [ABSTRACT FROM AUTHOR]
- Published
- 2012
42. Untangling a Darriwilian (Middle Ordovician) palaeoecological event in Baltoscandia: conodont faunal changes across the ‘Täljsten’ interval.
- Author
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Mellgren, Johanna I. S. and Eriksson, Mats E.
- Abstract
Conodont faunal dynamics and high-resolution biostratigraphy in the lithologically and faunally anomalous ‘Täljsten’ succession, which spans the Darriwilian Lenodus variabilis–Yangtzeplacognathus crassus Zone boundary, were investigated in a 2·5 m-thick section on Mt Kinnekulle that includes an interval yielding fossil meteorites and extraterrestrial chromite. The previous interpretation that this interval reflects a regression is consistent with the occurrence and abundance patterns of some conodont taxa. The disappearance of e.g., Periodon, suggests that the regression began prior to the deposition of the grey ‘Täljsten’. The transition from red to grey limestone coincides with a conspicuous faunal re-arrangement. The lower half of the ‘Täljsten’ reflects a gradual shallowing favourable for some taxa, such as Lenodus, and the immigration of Microzarkodina cf. ozarkodella and Histiodella holodentata. In the middle of the ‘Täljsten’ interval, coinciding with the appearance of abundant cystoids, conditions became less hospitable for conodonts, resulting in a low diversity and low abundance fauna, which occurs to the top of the interval. The overlying red limestone, apparently deposited during a deepening event, marks a return to pre-‘Täljsten’ conditions with a re-organised fauna. The close correlation between the lithologic shifts and conodont faunal changes demonstrates the usefulness of conodonts as environmental indicators. [ABSTRACT FROM PUBLISHER]
- Published
- 2009
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43. Graptolite and conodont biostratigraphy of the upper Telychian-lower Sheinwoodian (Llandovery-Wenlock) strata, Jabalón River section, Corral de Calatrava, central Spain.
- Author
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LOYDELL, D. K., SARMIENTO, G. N., ŠTORCH, P., and GUTIÉRREZ-MARCO, J. C.
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GRAPTOLITES , *CONODONTS , *BIOSTRATIGRAPHY , *FOSSIL animals - Abstract
A graptolite biostratigraphy is erected for the upper Telychian (upper crenulata Biozone) to lower Sheinwoodian (riccartonensisor dubiusBiozone) strata of the Jabalón River section, Spain. Two unconformities are recognized in the section: one between the lapworthiand murchisonibiozones; the other between the murchisoniand riccartonensisbiozones. These unconformities coincide with intervals of lowered eustatic sea-level. Graptolite assemblages include both cosmopolitan taxa and some which have been recorded previously from Morocco and/or other Spanish sections. At some stratigraphical levels Pristiograptusor Euroclimacisspecies are abundant; Monoclimacis, Streptograptusand Mediograptusspecies are generally uncommon. Conodonts were examined from the upper spiralisthrough to lower murchisoniBiozone; the occurrences of Pterospathodus amorphognathoidesare consistent with the species' known range elsewhere. Four new graptolite species are described: Euroclimacis jabalonensis, E. hamata, Monoclimacis flexaand Stimulograptus pradoi. [ABSTRACT FROM AUTHOR]
- Published
- 2009
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44. Morphology, evolution and stratigraphic distribution in the Middle Ordovician conodont genus Microzarkodina.
- Author
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Löfgren, Anita and Tolmacheva, Tatiana
- Abstract
Microzarkodina is a genus of mainly Middle Ordovician conodonts that has its centre of distribution in Baltoscandia, and much less commonly occurs in southern China, Australia, Argentina and Laurentia. In Baltica a series of species, Microzarkodina russica n. sp., M. flabellum, M. parva, M. bella, M. hagetiana and M. ozarkodella, established themselves successfully. The succession of species ranges from just below the base of the Middle Ordovician (M. russica) to the upper part of the Middle Ordovician (M. ozarkodella). The species are frequently used for biostratigraphical purposes. The largely contemporaneous species Microzarkodina bella and M. hagetiana probably both evolved from M. parva and mostly occurred in separate areas. Microzarkodina ozarkodella probably evolved from M. hagetiana. This present investigation is based on a total of 94,208 elements, collected from 20 sections and one drill-core site in Sweden, one drill-core site and one outcrop in Estonia and two sections in the St Petersburg area in Russia. The Microzarkodina apparatus probably consisted of 15 or 17 elements: four P, two or four M and nine S elements. The S elements include different Sa, Sb1, Sb2, and Sc element types. [ABSTRACT FROM PUBLISHER]
- Published
- 2008
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45. Biostratigraphic data from the Çetmi Melange, northwest Turkey: Palaeogeographic and tectonic implications
- Author
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Beccaletto, L., Bartolini, A.-C., Martini, R., Hochuli, P.A., and Kozur, H.
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SEDIMENTARY rocks , *PETROLOGY , *PLATE tectonics , *CRYSTALLINE rocks - Abstract
Abstract: The Çetmi accretionary melange is cropping out in the Biga Peninsula of northwest Turkey. It is characterised by an isolated position, relatively far from the accretion complexes of the nearest suture zones, which raises the question of its lateral correlations. A detailed biostratigraphic investigation of the limestone and radiolarite blocks and the matrix of the Çetmi melange allowed to propose a solution for this palaeogeographic problem. Scarce red nodular limestones in the Han Bulog facies represent the oldest lithology in the melange. Their Late Scythian–Ladinian age is based on Chiosella gondolleloides, the co-occurrence of Gladigondolella sp. and Nicoraella cf. kockeli, and Paragondolella fuelopi. Light grey limestone blocks are a characteristic feature of the Çetmi melange. They occur in two distinct facies. Facies A consists of packstone to grainstone, and is characterised by unsorted and poorly washed pelbiosparites. Facies B consists of wackestone to packstone, and is characterised by poorly washed biopelmicrites to biopelsparites. The foraminiferal assemblage of Facies A, containing Triasina hantkeni, is of Late Norian to Rhaetian age. The foraminiferal assemblage of Facies B never contains T. hantkeni, and is characteristic of a Late Triassic (Carnian? to Norian–Rhaetian) age. Radiolarian cherts are widely distributed in the Çetmi melange. They record fully pelagic sedimentation from the Upper Bajocian to the Aptian. The matrix of the Çetmi melange consists of brown to black shales, sometimes silty or siliceous, intercalated with dark grey greywackes. Palynomorphs of one sample of brownish silty shale yielded an Early to Middle Albian age, based on the co-occurrence of several dinoflagellate cysts. The age of the matrix, representing the youngest lithology within the melange, and of the unconformable overlaying section (latest Albian–Cenomanian) indicate that the melange-forming process stopped between the Early Albian and the latest Albian–Cenomanian. At a regional scale, the Çetmi melange has little in common with the melanges from the İzmir–Ankara and Intra–Pontide sutures of northwestern Turkey precluding a direct correlation. On the other hand, the Çetmi melange shares several characteristics with the melange-like units of the eastern Rhodope Zone (Bulgaria and Greece), like a major Cenomanian transgression, the reworking of Triassic limestones and Middle Jurassic–Lower Cretaceous radiolarians, and the absence of Jurassic–Cretaceous passive margin lithologies. The occurrence of Rhodopian units on the Biga Peninsula suggests that the studied units represent an isolated fragment of the Rhodope Zone in NW Turkey. [Copyright &y& Elsevier]
- Published
- 2005
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46. BASAL TISSUE STRUCTURE IN THE EARLIEST EUCONODONTS: TESTING HYPOTHESES OF DEVELOPMENTAL PLASTICITY IN EUCONODONT PHYLOGENY.
- Author
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Xi-Ping Dong, Donoghue, Philip C. J., and Repetski, John E.
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VERTEBRATES , *HISTOLOGY , *SKELETON , *DENTIN , *CONODONTS - Abstract
The hypothesis that conodonts are vertebrates rests solely on evidence of soft tissue anatomy. This has been corroborated by microstructural, topological and developmental evidence of homology between conodont and vertebrate hard tissues. However, these conclusions have been reached on the basis of evidence from highly derived euconodont taxa and the degree to which they are representative of plesiomorphic euconodonts remains an open question. Furthermore, the range of variation in tissue types comprising the euconodont basal body has been used to establish a hypothesis of developmental plasticity early in the phylogeny of the clade, and a model of diminishing potentiality in the evolution of development systems. The microstructural fabrics of the basal tissues of the earliest euconodonts (presumed to be the most plesiomorphic) are examined to test these two hypotheses. It is found that the range of microstructural variation observed hitherto was already apparent among plesiomorphic euconodonts. Thus, established histological data are representative of the most plesiomorphic euconodonts. However, although there is evidence of a range in microstructural fabrics, these are compatible with the dentine tissue system alone, and the degree of variation is compatible with that seen in clades of comparable diversity. [ABSTRACT FROM AUTHOR]
- Published
- 2005
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47. Conodont biostratigraphy and faunal assemblages in radiolarian ribbon-banded cherts of the Burubaital Formation, West Balkhash Region, Kazakhstan.
- Author
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Tolmacheva, Tatiana, Holmer, Lars, Popov, Leonid, and Gogin, Ivan
- Subjects
- *
CONODONTS , *ORDOVICIAN stratigraphic geology , *PALEOZOIC stratigraphic geology , *FOSSIL animals - Abstract
Biostratigraphical study of the early to mid-Ordovician conodont fauna from ribbon-banded radiolarian cherts of the middle Burubaital Formation in Central Kazakhstan reveals an almost complete succession of conodont biozones from the late Tremadocian to the early Darriwilian. During this interval, biosiliceous sediments were deposited in basinal environments, inhabited by lingulate brachiopods, sponges, pterobranchs and caryocaridids in conditions of high fertility and primary productivity of surface water. The community structure of taxonomically diverse conodont assemblages typifying open oceanic environments is not significantly different from that of epicratonic basins of the North Atlantic conodont province. The regional increase of oxygenated bottom waters at the base of the Oepikodus evae Biozone is possibly related to considerable changes in palaeo-oceanographical circulation patterns. The finds of three natural clusters of Prioniodus oepiki (McTavish) enable us to propose an emended diagnosis of this species. [ABSTRACT FROM AUTHOR]
- Published
- 2004
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48. Variation in the outline and distribution of epithelial cell imprints on the surface of polygnathacean conodont elements.
- Author
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Zhuravlev, Andrey V.
- Subjects
- *
CONODONTS , *REGENERATION (Biology) - Abstract
The elements of many conodont taxa exhibit a polygonal surface micro-ornamentation. Four main types are recognized (striation, linear texture, regular (idiomorphic) texture and granular texture) and their distribution over the conodont elements of different morphology is considered. The intraspecific (ontogenetic and ecological) and interspecific (phylogenetic) causes of the reticulation texture variations are also considered. [ABSTRACT FROM AUTHOR]
- Published
- 2001
- Full Text
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49. CONODONTS FROM THE LOWER TRIASSIC SEQUENCE OF CENTRAL DOLPO, NEPAL
- Author
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NICORA, ALDA
- Subjects
lcsh:Geology ,Conodonta ,lcsh:Paleontology ,Stratigraphy ,Lower Triassic ,lcsh:QE1-996.5 ,Scythian ,Central Dolpo ,Nepal ,lcsh:QE701-760 - Abstract
In the present paper, the conodont fauna from three detailed sections surveyed in the Lower Triassic sequence of Central Dolpo, Nepal (Tarap-Atali area) is illustrated. Combining faunas from the three sections, it was possible to recognize a succession of faunal events that covers most of the Scythian and the Lower Anisian. In the whole, 11 faunas have been recognized and discussed., Rivista Italiana di Paleontologia e Stratigrafia (Research In Paleontology and Stratigraphy), V. 97, N. 3-4
- Published
- 2017
50. Global climate changes account for the main trends of conodont diversity but not for their final demise.
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Ginot, Samuel and Goudemand, Nicolas
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- *
CLIMATE change , *COMPETITION (Biology) , *ICE sheets , *CONTINENTAL shelf , *FOSSILS , *ORDOVICIAN Period - Abstract
Conodonts, one of the longest-lived early groups of vertebrates, have a very complete fossil record ranging from the late Cambrian to the end of the Triassic and persisted through many global climatic and biotic events. In this paper, we analyse a large dataset harvested from the Paleobiology Database to compute global diversity curves at the generic level and explore patterns of conodont paleogeographic distribution. Our results partly confirm the most prominent findings of earlier studies including the occurrence of an Ordovician acme, a Permian nadir and a short-lived Triassic recovery. Major peaks of origination were found in the Early Ordovician and Early Triassic, while major extinctions occurred in the Upper Ordovician and Pennsylvanian. Paleogeographical extent of conodonts was impacted by i) the position of paleo-continents (notably impacting the latitudinal gradient of diversity), ii) the available continental shelf area and iii) ice sheets expansion. Diversity trends were mostly impacted by transitions between hothouse and icehouse ages, with major glaciations and associated marine regressions co-occurring with major extinctions. The influence of global sea level was less marked than that of temperature. However, the final demise of conodonts at the end of the Triassic did not coincide with either a major glaciation or marine regression. This supports the view that extinction of the group was mostly due to biotic factors such as competition with 'Mesozoic' taxa. • Conodont biodiversity was significantly impacted by sea-level and sea temperature; • Hit by end-Ordovician and end-Carboniferous extinction peaks; • Major extinctions were related to glaciation and sea-level drop; • Abiotic context of final extinction was different, suggesting biotic effects. [ABSTRACT FROM AUTHOR]
- Published
- 2020
- Full Text
- View/download PDF
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