Uchman et al.—New vermetid attachment trace from a Miocene rocky coast Recent vermetids live in tropical and temperate marine
waters between 44°N and 44°S, where they can form small reefs (Safriel, 1975; Schiaparelli and Cattaneo-Vietti, 1999; Silenzi et al., 2004; Schiaparelli et al., 2006). Generally, the period between 17Ma and 15Ma (Pińczów Formation, which can be related to the late phase of this because the overlying Miocene series is dated to NN5–NN6; see Radwański and Górka, 2008) is referred to the Middle Miocene Climatic Optimum, which is characterized by global warmth, high content of CO2 in the atmosphere, and a significant decrease in the Antarctic icecap (Foster et al., 2012). As evidenced by data on echinoids, the temperature rose up to tropical levels (sea surface temperatures 16–17°C during winter and up 28°C during summer) from the Karpatian (late Burdigalian) stage to the early Badenian optimum for the Central Paratethys, but the Carpathian Foredeep remained in the temperate climate zone (Kroh, 2007). However, data on facies from the eastern part of the Carpathian Foredeep (Stebnyk Formation, Ukraine) suggest that the increase in temperature also touched this region (Oszczypko et al., 2016). Only local, colder waters related to an upwelling are interpreted for the Paratethys sea at that time (Key et al., 2013). According to Bałuk and Radwański (1977), the slightly younger biota of the nearby Korytnica Clay (NN6) suggests tropical or subtropical environment. However, common occur- rences of echinoids and large foraminifera in the lower Badenian deposits that purportedly might suggest thermal conditions typical of subtropical or tropical climate are questioned by some authors. Studencki (1999) and Randazzo et al. (1999) suggested that paleo-temperature in the Paratethys basin during that time was rather typical of moderate climatic zones, on the border with the subtropical zone. This is suggested by poorly developed coral reefs, scarcity of green algae, and inorganic calcareous grains, especially ooids. According to Studencki (1999) and Randazzo et al. (1999), red algae, bryozoans, and mollusks that are very common in the lower Badenian deposits are typical of the rhodalgal biolithofacies, which occurs in Recent moderate climatic zones (e.g., near the coast of Scotland). Studencki (1999) postulated that the strong expansion of fauna known from the Korytnica Clay and the Heterostegina Sand, including large mollusks and large foraminifera, was a local effect of peculiar topographic conditions during the climatic optimum. The latitude of Skotniki (recently N50°25') during sedimentation of the gravelstone might be lower by 10° or more (e.g., Vrielynck et al., 1997). This, in coincidence with the Middle Miocene Climatic Optimum, suggests that the temperature of waters in the Paratethys Sea on the northern margin of the Carpathian Foredeep was higher at that time than the Atlantic waters in the same latitudes at present. Such waters were inhabited by vermetid gastropods, the shells of which are preserved and have small traces of Renichnus and the larger trace Spirolites n. igen.
Conclusions
Spirolites radwanskii is a new ichnogenus and ichnospecies of a spiral bioerosion trace in a Miocene rocky (limestone) substrate. Its morphological features (initial dipping into the rock, increasing in size, steep emerging from the substrate, second- order annuli, direction of coiling, erosion of the former part)
893
point to vermetid gastropods as the trace makers, resembling the recent Dendropoma. The trace fossil occurs within the Entobia ichnofacies and was produced in very shallow, warm, and clean waters in the Miocene rocky shore of the Paratethys Sea of the Carpathian Foredeep.
Acknowledgments
Jagiellonian University (DSC funds, no DS/MND/WbiNoZ/ ING/2/2013) supported the studies by M.S. on the Miocene rocks in the Carpathian Foredeep; (DS funds K/ZDS/005424 for A.U.). A previous version of the paper benefitted from critical reviews of M. Wisshak and M. Wilson.
References
Alexandrowicz, S.W., Garlicki, A., and Rutkowski, J., 1982, Podstawowe jednostki litostratygraficzne miocenu zapadliska przedkarpackiego: Kwartalnik Geologiczny, v. 26, p. 470–471.
Bałuk, W., and Radwański, A., 1977, Organic communities and facies development of the Korytnica basin (Middle Miocene; Holy Cross Mountains, Central Poland): Acta Geologica Polonica, v. 27, p. 85–123.
Beuck, L., López Correa, M., and Freiwald, A., 2008, Biogeographical distribution of Hyrrokkin (Rosalinidae, Foraminifera) and its host-specific morphological and textural trace variability, in Wisshak, M., and Tapanila, L., ed., Current Developments in Bioerosion: Berlin, Heidelberg, Springer, p. 329–360.
Biondi Giunti, S., 1859, Descrizione di alcune specie malacologiche nuove che vivono nel nostro litorale: Atti dell’Accademia Gioenia di Scienze Naturali, v. 14, p. 113–124.
Boekschoten, G.J., 1966, Shell borings of sessile epibiontic organisms as palaeoecoligical guides (with exanples from Dutch coast): Palaeo- geography, Palaeoclimatology, Palaeoecology, v. 2, p. 333–379.
Boettger, O., 1907, Zur Kentnis der Fauna der mittelmiocanen Schichten von Kostej im Krassö-Szörényer Komitat: Verhandlungen und Mitteilungen des siebenburgischen Vereins fur Naturwissenschaften zu Hermannstadt, v. 55, p. 101–217.
Bromley, R.G., 1978, Bioerosion of Bermuda reefs: Palaeogeography, Palaeoclimatology, Palaeoecology, v. 23, p. 169–197.
Bromley, R.G., 2008, Trace fossil Podichnus obliquus, attachment scar of the brachiopod Terebratulina retusa: Pleistocene, Rhodes, Greece: Fossils and Strata, v. 54, p. 227–230.
Bromley, R.G., and Asgaard, U., 1993a, Endolithic community replacement on a Pliocene rocky coast: Ichnos, v. 2, p. 96–116.
Bromley, R.G., and Asgaard, U., 1993b, Two bioerosion ichnofacies produced by early and late burial associated with sea-level change: Geologische Rundschau, v. 82, p. 276–280.
Bromley, R.G., and D’Alessandro, A., 1983, Bioerosion in the Pleistocene of southern Italy: ichnogenera Caulostrepsis and Maeandropolydora: Rivista Italiana di Paleontologia e Stratigrafia, v. 89, p. 283–309.
Bromley, R.G., and D’Alessandro, A., 1984, The ichnogenus Entobia from the Miocene, Pliocene and Pleistocene of southern Italy: Rivista Italiana di Paleontologia e Stratigrafia, v. 90, p. 227–296.
Bromley, R.G., and Heinberg, C., 2006, Attachment strategies of organisms on hard substrates: a palaeontological view: Palaeogeography, Palaeoclima- tology, Palaeoecology, v. 232, p. 429–453.
Bromley, R.G., and Surlyk, F., 1973, Borings produced by brachiopod pedicles, fossil and Recent: Lethaia, v. 6, p. 349–365.
Bronn, H.G., 1837–1838, Lethaia Geognostica oder Abbildungen und Bes- chreibungen der für die Gebirgs-Formationen bezeichnendsten Versteiner- ungen: Stuttgart: Schweizerbart, 1, 350 p.
Buatois, L., Wisshak, M., Wilson, M.A., and Mángano, G., 2017, Categories of architectural designs in trace fossils: a measure of ichnodisparity: Earth-Science Reviews, v. 164, p. 102–181.
Clarke, J.M., 1908, The beginnings of dependent life: New York State Museum Bulletin, v. 121, p. 146–169.
Foster, G.L., Lear, C.H., and Rae, J.W.B., 2012, The evolution of pCO2, ice volume and climate during the middle Miocene: Earth and Planetary
Scientific Letters, v. 341–344, p. 243–254.
Galinou-Mitsoudi, S., and Sinis, A.I., 1995, Age and growth of Lithophaga lithophaga (Linnaeus, 1758) (Bivalvia: Mytilidae), based on annual growth lines in the shell: Journal of Molluscan Studies, v. 61, p. 435–453.
Galinou-Mitsoudi, S., and Sinis, A. I., 1997, Population dynamics of the date mussel, Lithophaga lithophaga (L., 1758) (Bivalvia: Mytilidae), in the
Page 1 |
Page 2 |
Page 3 |
Page 4 |
Page 5 |
Page 6 |
Page 7 |
Page 8 |
Page 9 |
Page 10 |
Page 11 |
Page 12 |
Page 13 |
Page 14 |
Page 15 |
Page 16 |
Page 17 |
Page 18 |
Page 19 |
Page 20 |
Page 21 |
Page 22 |
Page 23 |
Page 24 |
Page 25 |
Page 26 |
Page 27 |
Page 28 |
Page 29 |
Page 30 |
Page 31 |
Page 32 |
Page 33 |
Page 34 |
Page 35 |
Page 36 |
Page 37 |
Page 38 |
Page 39 |
Page 40 |
Page 41 |
Page 42 |
Page 43 |
Page 44 |
Page 45 |
Page 46 |
Page 47 |
Page 48 |
Page 49 |
Page 50 |
Page 51 |
Page 52 |
Page 53 |
Page 54 |
Page 55 |
Page 56 |
Page 57 |
Page 58 |
Page 59 |
Page 60 |
Page 61 |
Page 62 |
Page 63 |
Page 64 |
Page 65 |
Page 66 |
Page 67 |
Page 68 |
Page 69 |
Page 70 |
Page 71 |
Page 72 |
Page 73 |
Page 74 |
Page 75 |
Page 76 |
Page 77 |
Page 78 |
Page 79 |
Page 80 |
Page 81 |
Page 82 |
Page 83 |
Page 84 |
Page 85 |
Page 86 |
Page 87 |
Page 88 |
Page 89 |
Page 90 |
Page 91 |
Page 92 |
Page 93 |
Page 94 |
Page 95 |
Page 96 |
Page 97 |
Page 98 |
Page 99 |
Page 100 |
Page 101 |
Page 102 |
Page 103 |
Page 104 |
Page 105 |
Page 106 |
Page 107 |
Page 108 |
Page 109 |
Page 110 |
Page 111 |
Page 112 |
Page 113 |
Page 114 |
Page 115 |
Page 116 |
Page 117 |
Page 118 |
Page 119 |
Page 120 |
Page 121 |
Page 122 |
Page 123 |
Page 124 |
Page 125 |
Page 126 |
Page 127 |
Page 128 |
Page 129 |
Page 130 |
Page 131 |
Page 132 |
Page 133 |
Page 134 |
Page 135 |
Page 136 |
Page 137 |
Page 138 |
Page 139 |
Page 140 |
Page 141 |
Page 142 |
Page 143 |
Page 144 |
Page 145 |
Page 146 |
Page 147 |
Page 148 |
Page 149 |
Page 150 |
Page 151 |
Page 152 |
Page 153 |
Page 154 |
Page 155 |
Page 156 |
Page 157 |
Page 158 |
Page 159 |
Page 160 |
Page 161 |
Page 162 |
Page 163 |
Page 164 |
Page 165 |
Page 166 |
Page 167 |
Page 168 |
Page 169 |
Page 170 |
Page 171 |
Page 172 |
Page 173 |
Page 174 |
Page 175 |
Page 176 |
Page 177 |
Page 178 |
Page 179 |
Page 180 |
Page 181 |
Page 182 |
Page 183 |
Page 184 |
Page 185 |
Page 186 |
Page 187 |
Page 188 |
Page 189 |
Page 190 |
Page 191 |
Page 192 |
Page 193 |
Page 194 |
Page 195 |
Page 196 |
Page 197 |
Page 198 |
Page 199 |
Page 200 |
Page 201 |
Page 202 |
Page 203 |
Page 204 |
Page 205 |
Page 206 |
Page 207