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M. Antczak , M. Stachacz, M. Ruciński, and M. Matysik
Geology
Location of the study area – Palaeogeographic map of the Germanic
Basin in the Middle Triassic. The Upper Silesia Region (white rectangle)
was situated close to the Tethys Ocean (after Matysik, 2004).
Geology
Location of the study area – Present outcrop distribution of the Middle Triassic
(Muschelkalk) carbonates in the Upper Silesia Region (Southern Poland) (after
Matysik, 2004).
Vertebrate material for preliminary studies was collected
from outcrops marked with red arrows.
Generalized stratigraphic section for the
Lower–Middle Muchelkalk of Upper Silesia,
showing thickness, overall lithological
character, provisional formation names and
range of epigenetic dolomitization (after
Matysik, 2014).
Project goals
Consideration of stratigraphic,
geographic and
environmental changes in
taxonomical composition
in the Middle Triassic sea,
owing to analysis of different
lithostratigraphic units in a
dozen localities.
A: two facies: limestone with numerous bivalve shells (upper strata) and
crinoids (lower strata); B: Traktowa street quarry in Dąbrowa Górnicza,
C: Górzysta street quarry in Dąbrowa Górnicza.
A
CB
Establishing the taxonomical variety of fish
and reptile remains will be the base of the
description of ecological diversity and
deposition character.
Ats-scientific.com
Viame.pl
The collected material includes both micro- and macrofossils. Microfossils were
picked up under the binocular after dissolution of the crushed sediment samples
in the 10% acetic acid.
Macrofossils were manually prepared by students of the Jagiellonian University.
Material and methods
1. Dissolution 2. Sieving 3. Microscopic identification
Preliminary results
Preliminary results reported herein present part of the expected diversity of
small vertebrates (chondrichtyans, ichtiopterygians and reptiles) from
several localities as well as skeletal elements of larger reptiles, mostly
nothosaurids.
Medium-sized fossils (2-4 mm) from Płaza including ?bowfin (Amiidae)
toothplate (B), ichtiosaurian vertebra (C), reptilian humerus (D) and
nothosaurian tooth (E).
A B
C
D
E
exact localization of the outcrop
Preliminary results: macrofossils
Macrofossils from Żyglin include difficult for taxonomical identification reptilian long
bones fragments (e.g., J, K, L), placodontid tooth (P), ribs (M, C - gastralia), coracoid
(E), phalangee (F), thoracic vertebra (H) and possibly hybodontid spine (B).
BA C
D E F G H I
J K L
M N
O
P
Preliminary results: macrofossils
1cm
Macrofossils from different localities: hybodontid
spine – Hybodus (A) and reptilian long bone –
nothosaur femur (B), vertebra (C) and rib (D).
A
B
C
D
Preliminary results: microfossils (part 1)
Microfossils from Dąbrowa Górnicza (Koksownicza street) include
actinopterygian fish scales (A, D), teeth (G, I, J, K) and jaw fragments (?
E, F,) and chondrichtyan fish teeth (C, H). Some can be assinged to
family/genus level, e.g., Hybodus (C), Lissodus (H), Amiidae (F),
Severnichthys (G, J), Gyrolepis (K).
A B C
D E F G
H I J
K
Preliminary results: microfossils (part 2)
Microfossils from Dąbrowa Górnicza (Koksownicza street)
include actinopterygian fish scales (E), teeth (B, F, H, ?I) and
chondrichtyan fish teeth (C, G), spines (D) or (?reptilian) vertebra (A).
Some can be assinged to family/genus level, e.g., Duffinselache (C),
Macrosemiidae (E), Gyrolepis (B), Hybodontidae (D).
A D E F
B C
G H
I
exact localization of the outcrop
What can we conclude?
Fish and reptile diversity
correlates with different
ecological niches, thus it can
be used for description of
sediment (tempestite)
origin and transport.
Preliminary results reveal
occurrence of semi-aquatic
reptiles along with predatory
and durophagous fishes,
including some fresh-water
or brackish taxa. Ecological diversity of fishes on the example of
Cretaceous vertebrate microfossils from Iberia
(Blanco et al., 2016)
Terminology for description of
isolated teeth (Heckert, 2004).
Different faunas in different localities?
Żyglin – abundandt remains of large reptiles (nothosaurids, placodontids);
Płaza – small reptilian remains (nothosaurids, ichtiosaurids);
Dąbrowa Górnicza – microfossils of actinopterygians and sharks;
Winterswijk – pistosauroids and other large reptiles (Sander et al., 2013);
Gogolin, Lamerden – pachypleurosaurids + microfossils (Kowal-linka &
Bodzioch, 2012; Diedrich, 2015)
Possible geographic differences
Mixosaurus, N. Tamura
Possible stratigraphic differences
Different species in distinct stratigraphic units?
Röt (Olenkian) – pachypleurosaurids (Kowal-Linka & Bodzioch, 2012),
reptile eggshells (Kardynał et al., 2015);
Lower part of Muschelkalk (Anisian) – nothosaurids, ichtiosaurids;
Upper part of Muschelkalk (Lanidian) – nothosaurids, the most
abundant ichtyofauna.
Dactylosaurus, dinopedia.wikia.com
Summary
 Preliminary results confirm that Middle Triassic faunas of Southern
Poland are diverse and include actinopterygians, chondrichtyans and
different kinds of reptiles.
 Future studies considering large number of specimens from a dozen
localities and different stratigraphic units will allow reconstructing the
diversity of mid-Triassic environments in time and space.
 Large number of specimens will allow describing new species and verifying
the stratigraphic range of existing taxa. For example, preliminary results
suggest the occurrence of Amiidae (bowfin) fish, whose the oldest
representatives are known from Jurassic deposits (Grande & Bemis, 1998).
Amia, lets-fish.com
References
Antczak, M., Bodzioch, A. 2018. Diversity of fish scales in Late
Triassic deposits of Krasiejów (SW Poland). Paleontological
Research, 22(1): 91 100.─
Arratia, G., Schultze, H.-P. 2012. The macrosemiiform fish
companion of the Late Jurassic theropod Juravenator from
Schauhampten, Bavaria, Germany. Fossil Record, 15(1): 5 25.─
DOI: 10.1002/mmng.201200001.
Assmann, P. 1933. Die Stratigraphie der oberschlesischen Trias. Teil
1: Der Bundsandstein. Jarbuch der Königlich Preuβischen
Geologischen Landesanstalt, 34(1): 169 340.─
Diedrich, C. G. 2015. The vertebrates from the Lower Ladinian
(Middle Triassic) bonebed of Lamerden (Germany) as
palaeoenvironment indicators in the Germanic Basin. Open
Geoscience, 7: 755 782.─
Giordano, P. G., Arratia, G., Schultze, H. P., 2016. Scale
morphology and specialized dorsal scales of a new
teleosteomorph fish from the Aptian of West Gondwana. Fossil
Record, 19: 61 81.─
Grande, L., Bemis, W.E. 1998. A Comprehensive Phylogenetic
Study of Amiid Fishes (Amiidae) Based on Comparative Skeletal
Anatomy. An Empirical Search for Interconnected Patterns of
Natural History. Memoir (Society of Vertebrate Paleontology), 4:
1–679. JSTOR 3889331.
Houssaye, A., Scheyer, T. M., Kolb, C., Fisher, V., Sander, P. M.
2014. A new look at ichthyosaur long bone microanatomy and
histology: implications for their adaption to an aquatic
life. PLOS ONE, 9(4): 1 10.─ DOI: 10.1371/journal.pone.0095637.
Kardynał, K., Kowalski, J., Bodzioch, A., Kowal-Linka, M. 2015.
Remains of small vertebrates from the Röt (Lower Triassic) of
Gogolin (Opole region, Poland). XIV EAVP Meeting, 6─10 July,
2016, Haarlem, The Netherlands, abstractbook: 186.
Kowal-Linka, M., Bodzioch, A. 2012. New finds of vertebrate
remains from the Röt (Lower Triassic, Olenkian) in the vincinity
of Gogolin (Opole Silesia, southern Poland). [In:] E. Jagt-
Yazykova, J. W. M. Jagt, Bodzioch A., Konietzko-Meier D. (eds.),
Krasiejów – palaeontological inspiration, 70 80, ZPW “Plik”─
Bytom.
Landon, E. N. U., Duffin, C. J., Hildebrandt, C., Davies, T. G.,
Simms, M. J., Benton, M. J. 2017. The discovery of crinoids
and cephalopod hooklets in the British Triassic. Proceedings of
the Geologists Association, 128(3): 360 373.─
Matysik, M., 2014. Sedimentology of the ‘ore-bearing’ dolomite’ of
the Kraków-Silesia region (Middle Triassic, southern Poland).
Annales Societatis Geologorum Poloniae, 84: 81-112.
Märss, T., 2006. Exoskeletal ultrasculpture of early vertebrates.
Journal of Vertebrate Paleontology, 26: 235 252.─
Nordén, K. K., Duffin, C. J., Benton, M. J. 2015. A marine
vertebrate fauna from the Late Triassic of Somerset, and a
review of British placodonts. Proceedings of the Geologists
Association, 126: 564 581.─
Sander, P.M., Klein, N., Albers, P.C.H., Bickelmann, C.,
Winkelhorst, C. 2013. Postcranial morphology of a basal
Pistosauroidea (Sauropterygia) from the Lower Muschelkalk
of Winterswijk, The Netherlands. Paläontologische Zeitschrift.
DOI 10.1007/s12542-013-0181-5.
Shang, Q. H. 2007. New information on the dentition and tooth
replacement of Nothosaurus (Reptilia: Sauropterygia).
Palaeoworld, 16(1-3): 254 263.─ DOI:
10.1016/j.palwor.2007.05.007.
Slater, T. S., Duffin, C. J., Hildebrandt, C., Davies, T. G.,
Benton, M. J. 2016. Microvertebrates from multiple bone
beds in the Rhaetian of the M4–M5 motorway junction, South
Gloucestershire, U.K. Proceedings of the Geologists
Association, 127(4): 464 477.─

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Middle Triassic (Muschelkalk) micro- and macrovertebrate remains from southern Poland

  • 1. M. Antczak , M. Stachacz, M. Ruciński, and M. Matysik
  • 2. Geology Location of the study area – Palaeogeographic map of the Germanic Basin in the Middle Triassic. The Upper Silesia Region (white rectangle) was situated close to the Tethys Ocean (after Matysik, 2004).
  • 3. Geology Location of the study area – Present outcrop distribution of the Middle Triassic (Muschelkalk) carbonates in the Upper Silesia Region (Southern Poland) (after Matysik, 2004). Vertebrate material for preliminary studies was collected from outcrops marked with red arrows.
  • 4. Generalized stratigraphic section for the Lower–Middle Muchelkalk of Upper Silesia, showing thickness, overall lithological character, provisional formation names and range of epigenetic dolomitization (after Matysik, 2014).
  • 5. Project goals Consideration of stratigraphic, geographic and environmental changes in taxonomical composition in the Middle Triassic sea, owing to analysis of different lithostratigraphic units in a dozen localities. A: two facies: limestone with numerous bivalve shells (upper strata) and crinoids (lower strata); B: Traktowa street quarry in Dąbrowa Górnicza, C: Górzysta street quarry in Dąbrowa Górnicza. A CB Establishing the taxonomical variety of fish and reptile remains will be the base of the description of ecological diversity and deposition character.
  • 6. Ats-scientific.com Viame.pl The collected material includes both micro- and macrofossils. Microfossils were picked up under the binocular after dissolution of the crushed sediment samples in the 10% acetic acid. Macrofossils were manually prepared by students of the Jagiellonian University. Material and methods 1. Dissolution 2. Sieving 3. Microscopic identification
  • 7. Preliminary results Preliminary results reported herein present part of the expected diversity of small vertebrates (chondrichtyans, ichtiopterygians and reptiles) from several localities as well as skeletal elements of larger reptiles, mostly nothosaurids. Medium-sized fossils (2-4 mm) from Płaza including ?bowfin (Amiidae) toothplate (B), ichtiosaurian vertebra (C), reptilian humerus (D) and nothosaurian tooth (E). A B C D E exact localization of the outcrop
  • 8. Preliminary results: macrofossils Macrofossils from Żyglin include difficult for taxonomical identification reptilian long bones fragments (e.g., J, K, L), placodontid tooth (P), ribs (M, C - gastralia), coracoid (E), phalangee (F), thoracic vertebra (H) and possibly hybodontid spine (B). BA C D E F G H I J K L M N O P
  • 9. Preliminary results: macrofossils 1cm Macrofossils from different localities: hybodontid spine – Hybodus (A) and reptilian long bone – nothosaur femur (B), vertebra (C) and rib (D). A B C D
  • 10. Preliminary results: microfossils (part 1) Microfossils from Dąbrowa Górnicza (Koksownicza street) include actinopterygian fish scales (A, D), teeth (G, I, J, K) and jaw fragments (? E, F,) and chondrichtyan fish teeth (C, H). Some can be assinged to family/genus level, e.g., Hybodus (C), Lissodus (H), Amiidae (F), Severnichthys (G, J), Gyrolepis (K). A B C D E F G H I J K
  • 11. Preliminary results: microfossils (part 2) Microfossils from Dąbrowa Górnicza (Koksownicza street) include actinopterygian fish scales (E), teeth (B, F, H, ?I) and chondrichtyan fish teeth (C, G), spines (D) or (?reptilian) vertebra (A). Some can be assinged to family/genus level, e.g., Duffinselache (C), Macrosemiidae (E), Gyrolepis (B), Hybodontidae (D). A D E F B C G H I exact localization of the outcrop
  • 12. What can we conclude? Fish and reptile diversity correlates with different ecological niches, thus it can be used for description of sediment (tempestite) origin and transport. Preliminary results reveal occurrence of semi-aquatic reptiles along with predatory and durophagous fishes, including some fresh-water or brackish taxa. Ecological diversity of fishes on the example of Cretaceous vertebrate microfossils from Iberia (Blanco et al., 2016) Terminology for description of isolated teeth (Heckert, 2004).
  • 13. Different faunas in different localities? Żyglin – abundandt remains of large reptiles (nothosaurids, placodontids); Płaza – small reptilian remains (nothosaurids, ichtiosaurids); Dąbrowa Górnicza – microfossils of actinopterygians and sharks; Winterswijk – pistosauroids and other large reptiles (Sander et al., 2013); Gogolin, Lamerden – pachypleurosaurids + microfossils (Kowal-linka & Bodzioch, 2012; Diedrich, 2015) Possible geographic differences Mixosaurus, N. Tamura
  • 14. Possible stratigraphic differences Different species in distinct stratigraphic units? Röt (Olenkian) – pachypleurosaurids (Kowal-Linka & Bodzioch, 2012), reptile eggshells (Kardynał et al., 2015); Lower part of Muschelkalk (Anisian) – nothosaurids, ichtiosaurids; Upper part of Muschelkalk (Lanidian) – nothosaurids, the most abundant ichtyofauna. Dactylosaurus, dinopedia.wikia.com
  • 15. Summary  Preliminary results confirm that Middle Triassic faunas of Southern Poland are diverse and include actinopterygians, chondrichtyans and different kinds of reptiles.  Future studies considering large number of specimens from a dozen localities and different stratigraphic units will allow reconstructing the diversity of mid-Triassic environments in time and space.  Large number of specimens will allow describing new species and verifying the stratigraphic range of existing taxa. For example, preliminary results suggest the occurrence of Amiidae (bowfin) fish, whose the oldest representatives are known from Jurassic deposits (Grande & Bemis, 1998). Amia, lets-fish.com
  • 16. References Antczak, M., Bodzioch, A. 2018. Diversity of fish scales in Late Triassic deposits of Krasiejów (SW Poland). Paleontological Research, 22(1): 91 100.─ Arratia, G., Schultze, H.-P. 2012. The macrosemiiform fish companion of the Late Jurassic theropod Juravenator from Schauhampten, Bavaria, Germany. Fossil Record, 15(1): 5 25.─ DOI: 10.1002/mmng.201200001. Assmann, P. 1933. Die Stratigraphie der oberschlesischen Trias. Teil 1: Der Bundsandstein. Jarbuch der Königlich Preuβischen Geologischen Landesanstalt, 34(1): 169 340.─ Diedrich, C. G. 2015. The vertebrates from the Lower Ladinian (Middle Triassic) bonebed of Lamerden (Germany) as palaeoenvironment indicators in the Germanic Basin. Open Geoscience, 7: 755 782.─ Giordano, P. G., Arratia, G., Schultze, H. P., 2016. Scale morphology and specialized dorsal scales of a new teleosteomorph fish from the Aptian of West Gondwana. Fossil Record, 19: 61 81.─ Grande, L., Bemis, W.E. 1998. A Comprehensive Phylogenetic Study of Amiid Fishes (Amiidae) Based on Comparative Skeletal Anatomy. An Empirical Search for Interconnected Patterns of Natural History. Memoir (Society of Vertebrate Paleontology), 4: 1–679. JSTOR 3889331. Houssaye, A., Scheyer, T. M., Kolb, C., Fisher, V., Sander, P. M. 2014. A new look at ichthyosaur long bone microanatomy and histology: implications for their adaption to an aquatic life. PLOS ONE, 9(4): 1 10.─ DOI: 10.1371/journal.pone.0095637. Kardynał, K., Kowalski, J., Bodzioch, A., Kowal-Linka, M. 2015. Remains of small vertebrates from the Röt (Lower Triassic) of Gogolin (Opole region, Poland). XIV EAVP Meeting, 6─10 July, 2016, Haarlem, The Netherlands, abstractbook: 186. Kowal-Linka, M., Bodzioch, A. 2012. New finds of vertebrate remains from the Röt (Lower Triassic, Olenkian) in the vincinity of Gogolin (Opole Silesia, southern Poland). [In:] E. Jagt- Yazykova, J. W. M. Jagt, Bodzioch A., Konietzko-Meier D. (eds.), Krasiejów – palaeontological inspiration, 70 80, ZPW “Plik”─ Bytom. Landon, E. N. U., Duffin, C. J., Hildebrandt, C., Davies, T. G., Simms, M. J., Benton, M. J. 2017. The discovery of crinoids and cephalopod hooklets in the British Triassic. Proceedings of the Geologists Association, 128(3): 360 373.─ Matysik, M., 2014. Sedimentology of the ‘ore-bearing’ dolomite’ of the Kraków-Silesia region (Middle Triassic, southern Poland). Annales Societatis Geologorum Poloniae, 84: 81-112. Märss, T., 2006. Exoskeletal ultrasculpture of early vertebrates. Journal of Vertebrate Paleontology, 26: 235 252.─ Nordén, K. K., Duffin, C. J., Benton, M. J. 2015. A marine vertebrate fauna from the Late Triassic of Somerset, and a review of British placodonts. Proceedings of the Geologists Association, 126: 564 581.─ Sander, P.M., Klein, N., Albers, P.C.H., Bickelmann, C., Winkelhorst, C. 2013. Postcranial morphology of a basal Pistosauroidea (Sauropterygia) from the Lower Muschelkalk of Winterswijk, The Netherlands. Paläontologische Zeitschrift. DOI 10.1007/s12542-013-0181-5. Shang, Q. H. 2007. New information on the dentition and tooth replacement of Nothosaurus (Reptilia: Sauropterygia). Palaeoworld, 16(1-3): 254 263.─ DOI: 10.1016/j.palwor.2007.05.007. Slater, T. S., Duffin, C. J., Hildebrandt, C., Davies, T. G., Benton, M. J. 2016. Microvertebrates from multiple bone beds in the Rhaetian of the M4–M5 motorway junction, South Gloucestershire, U.K. Proceedings of the Geologists Association, 127(4): 464 477.─

Editor's Notes

  1. M. MU. – Mid dle Muschelkalk; D. B – Diplopora Beds; TST – transgressive systems tract; HST – highstand systems tract; MFZ – maximum flooding zone; SB – sequence boundary. Sequence stratigraphy framework after Szulc (2000), lithostratigraphy of the Opole region after Assmann (1913, 1944) with later formalization by Bodzioch (1997), Niedźwiedzki (2000) and Kowal-Linka (2008).