Two new mammal localities within the Lower Cretaceous Ilek Formation of West Siberia, Russia

Two new mammal localities within the Lower Cretaceous Ilek Formation of West Siberia, Russia

Accepted Manuscript Title: Two new mammal localities within the Lower Cretaceous Ilek Formation of West Siberia, Russia Author: Alexander Averianov Al...

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Accepted Manuscript Title: Two new mammal localities within the Lower Cretaceous Ilek Formation of West Siberia, Russia Author: Alexander Averianov Alexey Lopatin Pavel Skutschas Sergey Leshchinskiy PII: DOI: Reference:

S0016-6995(15)00015-7 http://dx.doi.org/doi:10.1016/j.geobios.2015.02.004 GEOBIO 700

To appear in:

Geobios

Received date: Revised date: Accepted date:

10-10-2014 3-1-2015 3-2-2015

Please cite this article as: Averianov, A., Lopatin, A., Skutschas, P., Leshchinskiy, S.,Two new mammal localities within the Lower Cretaceous Ilek Formation of West Siberia, Russia, Geobios (2015), http://dx.doi.org/10.1016/j.geobios.2015.02.004 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

Two new mammal localities within the Lower Cretaceous Ilek Formation of West Siberia, Russia  Alexander Averianov a,b,*, Alexey Lopatin c, Pavel Skutschas b,d, Sergey Leshchinskiy b

Zoological Institute of the Russian Academy of Sciences, Universitetskaya nab. 1, 199034

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a

Saint Petersburg, Russia

Laboratory of Mesozoic and Cenozoic Continental Ecosystems, Tomsk State University,

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b

c

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Prospekt Lenina 36, 634050 Tomsk, Russia

Borissiak Paleontological Institute of the Russian Academy of Sciences, Profsoyuznaya 123,

Vertebrate Zoology Department, Saint Petersburg State University, Universitetskaya Nab.

7/9, 199034 Saint Petersburg, Russia

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d

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117997 Moscow, Russia

Corresponding editor: Gilles Escarguel.

Abstract

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* Corresponding author. E-mail address: [email protected] (A. Averianov).

Two new mammal localities have been discovered in the Lower Cretaceous Ilek

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Formation of West Siberia, Russia, during a field work in 2014. The Smolenskii Yar locality in the Chebula District of Kemerovo Province produced an upper molariform tooth (M2) of a Gobiconodontidae indet. The Ust’-Kolba locality in the Tisul’ District of Kemerovo Province yielded a lower molar (m2) of the zhangheotherian Kiyatherium sp. These are the ninth and tenth Mesozoic mammal localities for Russia. The Kiyatherium-bearing vertebrate assemblage from the Shestakovo 3 and Ust’-Kolba localities is likely to be the youngest within the Ilek Formation, reflecting the time after the extinction of the Tritylodontidae.

Keywords:

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Mammalia Gobiconodontidae Zhangheotherian Kiyatherium sp. Early Cretaceous Ilek Formation

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Siberia

1. Introduction

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A rich vertebrate fauna, including various dinosaurs and mammals, have been recovered during the last two decades at Shestakovo 1 and 3 localities from the Lower

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Cretaceous Ilek Formation in West Siberia (Maschenko and Lopatin, 1998; Alifanov et al., 1999; Tatarinov and Maschenko, 1999; Efimov and Leshchinskiy, 2000; Averianov and Fayngertz, 2001; Averianov and Voronkevich, 2002; Averianov et al., 2002, 2003a, b, 2006;

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Maschenko et al., 2003; Lopatin et al., 2005, 2009, 2010a, b; Averianov and Lopatin, 2008; Kurochkin et al., 2011; O'Connor et al., 2014; Skutschas, 2014). The Ilek Formation is widely

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distributed in West Siberia. Extensive exploration of various outcrops of this formation by the field parties of the Tomsk State University and affiliated colleagues led to the discovery of some other vertebrate localities, but so far only new localities within the Bol’shoi Kemchug

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River basin, Krasnoyarsk Territory, produced fossil mammals (Leshchinskiy and Fayngertz, 2001; Averianov et al., 2005).

Here we report on the discovery of two new mammal localities from the Ilek Formation in the Kiya River basin, Kemerovo Province, close to the Shestakovo localities

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(Fig. 1; Table 1). Both vertebrate localities, namely Ust’-Kolba and Smolenskii Yar, have been found during prospections in 2000 and 2001 (Leshchinskiy and Fayngertz, 2001). Some additional screen-washing was made at these localities in 2002 and 2005. The first mammal specimens have been found in 2011 after screen-washing of ~230 kg of matrix from Ust’Kolba locality and ~380 kg from Smolenskii Yar locality. These mammal specimens are described herein. The specimens are housed in the collection of the Laboratory of Mesozoic and Cenozoic Continental Ecosystems, Tomsk State University (LMCCE).

2. Geographic and geological setting

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The Ust’-Kolba locality (GPS coordinates: N 55°52’36.2’’, E 88°19’07.6’’) is a small quarry on the left bank of the Serta River near the Ust’-Kolba settlement, ~2 km upstream from the mouth of the river (Tisul’ District, Kemerovo Province). The visible section (Fig. 1(c)) starts at the altitude of ~187 m and encompass approximately 20 m of fluvial facies of the Ilek Formation. It is dominated by yellowish-green assorted sands with an admixture of pebble and gravel, confined mainly to the bottom of cross-bedded layers and lenses. Pebbles

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and gravel are presented by pellets (up to 0.1 m) of thick clays, silts, and carbonate nodules. Vertebrate fossils (scales, bone fragments, and teeth) are confined mainly to the gravel lenses

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at the bottom of the visible part of the section. These sediments represented a relatively high energy condition, but the preservation of the fossils, although fragmentary, indicates that they

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were not reworked.

The Smolenskii Yar locality (GPS coordinates: N 55°58’23.9’’, E 88°05’35.9’’) is

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confined to a natural outcrop on the right bank of Serta River, 1 km downstream from the Kursk-Smolenka settlement (Chebula District, Kemerovo Province). The section is similar to that of the Shestakovo 1 locality (Leshchinskiy et al., 1997). Eleven layers can be recognized

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in the section at the southwest part of the escarpment from the water level (Fig. 1(d); from bottom to top):

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1) Yellowish to green, assorted dense sand (> 2.5 m); 2) Green coarse-grained sand with dense pellets of clay, silt and carbonate nodules. The vertebrate fossils (mainly scales, bone fragments, and teeth) are confined to the roof of

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this layer which has a cross-bedded texture; 3) Yellowish to green, fine-grained dense sand. In some places there are small ripple flow textures. At the top there is a body of dense calcareous sandstone (up to 0.5 m) projecting from the outcrop as a cornice (~3.6 m);

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4) Dark gray compact clay (~0.3 m);

5) Yellowish to green fine to medium-sized dense sand (~0.7 m); 6) Bluish-gray stratified tight siltstone (~2.5 m); 7) Brown-red marly dense clay (~1.5 m); 8) Alternating layers of bluish-gray siltstone and brownish-red clay (~2 m); 9) Yellowish-green, fine-grained sand interbedded with gray siltstone (~5 m); 10) Alternating layers of bluish-gray siltstone and brownish-red clay (> 15 m); 11) Quaternary deposits (subaerial loam, sandy loam, and modern soil) (~1 m); The vertebrate assemblages from both localities are globally similar (Table 1). Most taxa are represented by isolated and usually fragmentary specimens. The most common fossils 3

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are fish scales. The salamanders are represented by postcranial elements. The turtles are surprisingly rare in the Ilek Formation, contrasting with the majority of other Cretaceous assemblages; the discussed localities yielded only small fragments of turtle plates likely belonging to the macrobaenid turtle cf. Kirgizemys sp., also known from the Shestakovo 1 locality from the same formation (Averianov et al., 2003a). The lizards and choristoderes are known from jaw fragments and isolated vertebrae; crocodyliforms are known from vertebrae,

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jaw fragments, and teeth. Only two pterosaur teeth have been found, one for each locality.

The dinosaurs are also represented, mostly by isolated teeth. A notable exception (from the

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Ust’-Kolba locality) is an elongated posterior caudal vertebra of a derived maniraptoran

theropod, showing a groove along the dorsal side of the neural arch and the ventral side of the

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centrum. This vertebra may belong to a troodontid, a family also known from the

Shestakovo 1 locality by isolated teeth (Averianov and Sues, 2007). Although the observed

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differences between the two vertebrate assemblages are likely to be of sampling origin, one important discrepancy seems to be real: teeth of the tritylodontid Xenocretosuchus sp. are quite common at the Smolenskii Yar locality, while they have not yet been found at the Ust’-

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Kolba locality.

MAMMALIA Linnaeus, 1758

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3. Systematic paleontology

GOBICONODONTIDAE Chow et Rich, 1984

Fig. 2(a-d)

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GOBICONODONTIDAE indet.

Referred specimen: LMCCE 1/2, left M2 missing the mesial cusp B and the mesial root. Smolenskii Yar locality, Chebula District, Kemerovo Province, Russia; Ilek Formation,

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Lower Cretaceous.

Measurements: width = 0.9 mm. Description: Cusp C is about twice lower than cusp A. Cusps are conjoined approximately up to the half of cusp A height. The missing mesial cusp B was evidently more separated from cusp A. In occlusal view, cusp C is transversely narrower than cusp A, while the distal part of the crown is wider than the middle part. There is a slight ectoflexus opposite to cusp A. At this place the labial cingulum is narrower than at its distal part. The tips of cusps A and C and the crest connecting cusp C with the cingulum are worn. The lingual cingulum is highly worn. The unworn distal portion of the lingual cingulum is rather thick. The distal root is robust, short, and mesiodistally compressed, as is typical in Gobiconodon. 4

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Remarks: The tooth is an upper molariform because of a complete cingulum around the crown. Comparing with the Mongolian species of Gobiconodon (Kielan-Jaworowska and Dashzeveg, 1998; Lopatin and Averianov, 2015), the tooth is an anterior molariform (M1 or M2) since the main cusps A, B, and C aligned longitudinally (while the mesial cusp B is missing, the reconstructed angle between these three cusps is ~175°). In more posterior molariforms (M3-5) these cusps angulated. Moreover, the relatively unreduced cusp C and

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mesiodistally compressed root allow identification of this specimen as an M2 (Lopatin and Averianov, 2015; on M1 the cusp C is distinctly smaller and the roots are round in cross

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section).

LMCCE 1/2 resembles M2 of G. hoburensis from the Lower Cretaceous of Mongolia

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(Lopatin and Averianov, 2015) in size and morphology. It differs by a slight ectoflexus and narrowed labial cingulum opposite to the main cusp A. LMCCE 1/2 differs from M2 of

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Gobiconodon sp. A from the Bol’shoi Kemchug 3 locality of the Ilek Formation in Krasnoyarsk Territory (Averianov et al., 2005: fig. 5E,F) by distal part of the crown wider than the middle part, much larger cusp C, and by the lack of the distal cusp D. The

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Gobiconodon sp. A from Bol’shoi Kemchug 3 may actually represent a distinct genus of Gobiconodontidae. There is an extensive collection of gobiconodontids from the

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Shestakovo 1 locality of the Ilek Formation, which is currently under study by the authors. Most likely, LMCCE 1/2 belongs to one of the undescribed new taxa from that locality.

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TRECHNOTHERIA McKenna, 1975

ZHANGHEOTHERIA Averianov, Martin et Lopatin, 2013 Genus Kiyatherium Maschenko, Lopatin et Voronkevich, 2002 Kiyatherium sp.

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Fig. 2(e-i)

Referred specimen: LMCCE 1/1, left m2. Ust’-Kolba locality, Tisul’ District, Kemerovo Province, Russia; Ilek Formation, Lower Cretaceous. Measurements: length = 1.8 mm; width = 1.0 mm. Description: The crown is D-shaped in occlusal view, with straight (slightly concave) lingual margin and convex labial margin. Cusp a is high and erect, perpendicular to the crown base. Side cusps b and c are placed lingually to cusp a, forming an angle of ~117°. Cusp c is about two-thirds of cusp a in height and somewhat curved distally. A considerable part of cusp b is removed by wear; possibly it was as high as cusp c. There is a very strong lingual cingulid connecting the distal cusp d with the mesiolingual cuspule e. Cusps b, c, d, and e are aligned 5

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along the lingual margin of the crown. Cusp d is distinct but not high. Cuspule e is smaller than cusp d. The mesiolabial cuspule f, if present, is completely worn. There is a slight embayment between the latter and cuspule e. There is a large wear facet along the entire labial side of cusp b, which extends on the mesial cuspules e and f. On cusp a there is only an apical wear facet. On cusp c there is an apical facet and a facet along the c-d ridge. Also there is a horseshoe-shaped facet on the embayment between the bases of cusps c and d. On the apex of

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cusp d there is a wear facet on the distal side. The roots are nearly equal in size, very robust

and long, with a terminal swelling before the end. The height of the roots is 1.6 times greater

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than the crown height. If the crown base oriented horizontally, the roots were slightly inclined distally. There is a thin bony lamina connecting the roots below the crown. The roots are more

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or less round in cross section. In a parasagittal plane (Fig. 2(f, h)) the roots are bent lingually. Remarks: The tooth is a lower molar based on the lack of a cingulid on the labial side. Lower

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molars of basal zhangheotherians (formerly “obtuse-angled” symmetrodontans) and gobiconodontids, which are likely to be closely related to the Trechnotheria (Lopatin and Averianov, 2015), have a similar design. In zhangheotherians the main cusps a, b, and c are

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more angulated while in gobiconodontids these cusps are almost aligned. In LMCCE 1/1 the angle between these cusps is ~117°, which allows referral of this specimen to the

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Zhangheotheria.

There are two taxa of zhangheotherians known from the Ilek Formation: Yermakia domitor Lopatin et al., 2005 from the Shestakovo 1 locality, and Kiyatherium cardiodens

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Maschenko, Lopatin et Voronkevich, 2002 from the Shestakovo 3 locality (Maschenko et al., 2002; Lopatin et al., 2005; Lopatin et al., 2010a). K. cardiodens is slightly larger than Y. domitor, and LMCCE 1/1 fits exactly the size range of the middle molars (m2 or m3) of the former taxon (Lopatin et al., 2010a). Moreover, it is similar to K. cardiodens by less

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angulation of molar cusps and much stronger lingual cingulid, while in Y. domitor the cusp angle of m2-3 is 102°-110° and the lingual cingulid is very faint (Lopatin et al., 2005). Thus attribution of LMCCE 1/1 to Kiyatherium seems to be firmly established, although it is left in open nomenclature due to the paucity of the available material. By its crown proportions, LMCCE 1/1 corresponds to the m2 of K. cardiodens. On m1 there is a greater height differential between the main and side cusps, and on m3-4 cusp c is more reduced. Also m2 is the transversely widest molar in the series, which agrees with a relatively wide crown in LMCCE 1/1. The swollen roots of LMCCE 1/1 likely reinforced the tooth implantation in the tooth sockets. A similar adaptation is characteristic for the stem mammal Morganucodon 6

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(Parrington, 1973). This is the first discovery of Kiyatherium outside its type locality (Shestakovo 3).

4. Discussion The two new Mesozoic mammal localities reported in this paper increases up to ten the number of the Mesozoic mammal localities for Russia (Lopatin and Averianov, 2006a,

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2009). Six of these localities are within the Lower Cretaceous Ilek Formation in West Siberia: two in the Bol’shoi Kemchug River basin in Krasnoyarsk Territory (localities Bol’shoi

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Kemchug 3 and Bol’shoi Terekhtyul’) and four in the Kiya River basin in Kemerovo Province (localities Shestakovo 1 and 3, Ust’-Kolba, and Smolenskii Yar). Although the synapsid fauna

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of the Ilek Formation is still insufficiently known, three assemblages can be recognized so far: 1) The localities within the Bol’shoi Kemchug River basin, with tritylodontids,

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gobiconodontids, and amphilestids;

2) The Shestakovo 1 and Smolenskii Yar localities, with tritylodontids, tegotheriids, gobiconodontids, amphidontids, and the zhangheotherian Yermakia;

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3) The Shestakovo 3 and Ust’-Kolba localities, with the zhangheotherian Kiyatherium. The first assemblage is likely to be the oldest. The second one is better known from

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the Shestakovo 1 locality since the Smolenskii Yar locality produced abundant tritylodontid remains and a single mammal specimen (a gobiconodontid) so far. The third assemblage is notable in the absence of tritylodontids, although the vertebrates from the Shestakovo 3

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locality have been sampled only by quarrying since the matrix there is not suitable for screenwashing. Thus its microvertebrate assemblage remains insufficiently known. The second and third assemblages may reflect different paleoenvironments or diachronous faunas. If the latter is correct, the third assemblage may illustrate the time after the local extinction of the

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Tritylodontidae. This event could be the global extinction event for this group, as the Tritylodontidae are unknown in younger rocks elsewhere. The Shestakovo area was possibly the last refugium for the tritylodontids. The abundance of tritylodontids in the Early Cretaceous of West Siberia may explain the absence of the multituberculate mammals there, which likely had the similar herbivorous diet. The mammal fauna from the Ilek Formation is also notable for absence of any tribosphenic or pretribosphenic taxa, which were present in the Early Cretaceous faunas of Asia (Shikama, 1947; Dashzeveg, 1975, 1979, 1994; Dashzeveg and Kielan-Jaworowska, 1984; Kielan-Jaworowska and Dashzeveg, 1989; Averianov and Skutschas, 2001; Ji et al.,

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2002; Li et al., 2005; Lopatin and Averianov, 2006b, 2007). The reason for this remains poorly understood.

Acknowledgements We thank students of the Tomsk University for the help with screen-washing. Special thanks to Anastasia Zelentsova and Lidia Kondratieva, the students who found the mammals

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teeth. We are grateful to Rodolphe Tabuce, Jin Meng and an anonymous reviewer for reading the manuscript and useful suggestions. This work was supported by the Tomsk State

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University Academic D.I. Mendeleev Fund Program and by the Russian Foundation for Basic

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Research (project 13-04-01401).

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Maschenko, E.N., Lopatin, A.V., 1998. First record of an Early Cretaceous triconodont mammal in Siberia. Bulletin de l'Institut Royal des Sciences Naturelles de Belgique, Sciences de la Terre 68, 233-236.

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Maschenko, E.N., Lopatin, A.V., Voronkevich, A.V., 2002. A new Early Cretaceous mammal from Western Siberia. Doklady Biological Sciences 386, 475–477.

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Maschenko, E.N., Lopatin, A.V., Voronkevich, A.V., 2003. A new genus of the tegotheriid docodonts (Docodonta, Tegotheriidae) from the Early Cretaceous of West Siberia. Russian Journal of Theriology 1, 75-81.

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McKenna, M.C., 1975. Towards a phylogenetic classification of the Mammalia, in: Luckett, W.P., Szalay, F.S. (Eds.), Phylogeny of the Primates. Plenum Press, New York, pp. 2146.

O'Connor, J.K., Averianov, A.O., Zelenkov, N.V., 2014. A confuciusornithiform (Aves,

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Pygostylia)-like tarsometatarsus from the Early Cretaceous of Siberia and a discussion of the evolution of avian hind limb musculature. Journal of Vertebrate Paleontology 34, 647-656.

Parrington, F.R., 1973. The dentition of the earliest mammals. Zoological Journal of the Linnean Society 52, 85-95. Shikama, T., 1947. Teilhardosaurus and Endotherium, new Jurassic Reptilia and Mammalia from the Husin coal-field, south Manchuria. Proceedings of the Japanese Academy 23, 76-84.

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Skutschas, P.P., 2014. Kiyatriton leshchinskiyi Averianov et Voronkevich, 2001, a crowngroup salamander from the Lower Cretaceous of Western Siberia, Russia. Cretaceous Research 51, 88-94. Tatarinov, L.P., Maschenko, E.N., 1999. [A find of an aberrant tritylodont (Reptilia, Cynodontia) in the Lower Cretaceous of Kemerovo Region]. Paleontologicheskii

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Zhurnal, 85-92.

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Table and Figure captions Table 1. Comparison of vertebrates assemblages from the Ust’-Kolba and Smolenskii Yar localities, Ilek Formation, Lower Cretaceous.

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Figure 1. Geographic and geological setting for the Ust’-Kolba and Smolenskii Yar localities. a. Map of Russia with the studied area shown by an asterisk. b. Detailed map showing

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position of the vertebrate localities: 1-3, Shestakovo 1 to 3; 4, Smolenskii Yar; 5, Ust’-Kolba (modified from Leshchinskiy and Fayngertz, 2001: fig. 15). c. Section at the Ust’-Kolba

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locality. d. Section at the Smolenskii Yar locality. Position of the vertebrate bearing level in

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each section is marked by an asterisk.

Figure 2. Mammalian teeth from the Smolenskii Yar (a-d) and Ust’-Kolba (e-i) localities, Ilek Formation, Lower Cretaceous. a-d. Gobiconodontidae indet., LMCCE 1/2, left M2, in

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occlusal (a, stereopair), lingual (b), distal(?) (c), and labial (d) views. e-i. Kiyatherium sp., LMCCE 1/1, left m2, in occlusal (e, stereopair), distal (f), lingual (g), mesial (h), and labial (i)

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views. For the stereopairs the anterior mesial end is up. A, C, and a-f are cusps of the upper

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and lower molar, respectively. Scale bar: 1 mm.

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Table 1 OK

Table 1.

Smolenskii Yar

+ +

+ +

+

+

+ + +

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+ + +

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+

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+

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+

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+

+

+ +

+ + + + + + +

+

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Ust’-Kolba

+

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Taxon Pisces Paleonisciformes indet. Amiiformes indet. Caudata cf. Kiyatriton sp. Testudines Testudines indet. Squamata Lacertilia indet. Choristodera Choristodera indet. Crocodyliformes Shartegosuchidae indet. “Protosuchia” indet. Pterosauria Ornithocheiridae indet. Istiodactylidae indet. Dinosauria Psittacosaurus sp. Stegosauria indet. Sauropoda indet. Therizinosauria indet. Troodontidae(?) indet. Theropoda indet. Tritylodontidae Xenocretosuchus sp. Mammalia Gobiconodontidae indet. Kiyatherium sp.

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Figure 1 OK

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Figure 2 OK

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