Conference PaperPDF Available

A new deep-water Decapod Crustacean faunule from the Early Miocene of the Styrian Basin, Slovenia

Authors:
  • Institute for Palaeobiology and Evolution, Slovenia

Abstract and Figures

Previously, decapods from the Miocene strata in the Slovenian part of the Styrian Basin were reported by Glaessner (1928) and Mikuž (2003). In this contribution we present a report on a new decapod crustacean faunule from the respective area.
Content may be subject to copyright.
21. posvetovanje slovenskih geologovGašparič & Hyžný, Abstract
1
A NEW DEEP-WATER DECAPOD CRUSTACEAN FAUNULE FROM THE EARLY
MIOCENE OF THE STYRIAN BASIN, SLOVENIA
Rok Gašparič 1 & Matúš Hyžný 2
1 Ljubljanska cesta 4j, 1241 Kamnik, Slovenija < rok.gasparic@gmail.com>
2 Department of Geology and Palaeontology, Faculty of Natural Sciences, Comenius University,
Mlynská dolina G1, Bratislava 842 15, Slovakia < hyzny.matus@gmail.com>
Previously, decapods from the Miocene strata in the Slovenian part of the Styrian
Basin were reported by Glaessner (1928) and Mikuž (2003). In this contribution we present a
report on a new decapod crustacean faunule from the respective area.
The studied locality is situated approximately 15 kilometers west of Maribor, along
the steep valley of the Drava River. The decapod bearing layers were exposed during road
renovation works on a local road connecting the towns of Ruše and Lovrenc na Pohorju and
are part of a Miocene sedimentary basin running from Maribor on the northern slopes of
Pohorje plutonic massif towards Radlje.
Fossil bearing micaceous laminated siltstones are part of the Ivnik beds (Mioč, 1972),
overlaying sequences of loosely bound chaotic conglomerates and sandstones. Conglomerates
are composed mainly of pebbles of metamorphic rock and Pohorje granodiorite (Pavšič &
Horvat, 2009). Results of nannoplankton sampling (Bartol et al., in print) indicate the
Karpatian age (nannoplankton zone NN4), based on coexistence of Sphenolithus
heteromorphus Deflandre, 1953 and Helicosphaera ampliaperta Bramlette and Wilcoxon,
1967.
21. posvetovanje slovenskih geologovGašparič & Hyžný, Abstract
2
Fig. 1.Geographical position of the fossil locality with simplified geological sketch.
The Karpatian signifies the beginning of the marine sedimentation regime in the
broader realm of the Central Paratethys and represents a short flooding event that resulted
from opening of a marine passage between the Paratethys and the Mediterranean Sea i.e.
Slovenian corridor (Rögl, 1998). Synrift tectonics with rapid subsidence of narrow elongated
sedimentation basins at the beginning of Karpatian (Jelen & Rifelj, 2003) and the described
foraminiferal assemblage indicate bathyal conditions with the basin depth exceeding 500
meters (Fodor, 2002). Our observation of decapod crustaceans and the associated assemblage
confirms the bathyal character of the investigated fauna.
The sample consists of 245 specimens of decapod crustaceans collected by one of the
authors (RG) and housed at the “Rok Gašparič paleontological collection”, part of
paleontological collections of Slovenian Museum of Natural History. Studied specimens are
compressed inside the siltstones and mainly retain the original cuticle. Many decapods are
still articulated which, considering their fragility, implies a very calm sedimentation
environment and excludes any greater post mortem transportation.
21. posvetovanje slovenskih geologovGašparič & Hyžný, Abstract
3
Preliminary results allow us to assign the investigated specimens to the following taxa:
Order Decapoda
Infraorder Axiidea
Family Callianassidae
Callianassa cf. michelottii MILNE EDWARDS, 1860 (Fig. 2.A)
The material consists of three specimens. Only major cheliped propodus (in one case
associated with dactylus) is preserved. The material differs from Callianassa michelottii in the
nature of lateral propodal surface. In C. michelottii it typically has long keel extending onto
the fixed finger accompanied with two furrows. In our material the keel is faint and the
furrows do not seem to be present. More and better preserved material may resolve the
affinities of the studied material.
Callianassa sp. (Fig. 2.B)
The material consists of three specimens. One of the specimens exhibits a major chela
(propodus articulated with dactylus its shape does not correspond to any other callianassid
specimen recovered at the locality).
Lepidophthalmus n. sp. (Fig. 2.C)
The material consists of 19 specimens. Usually major cheliped propodus is preserved;
sometimes articulated with dactylus. In one case major chela is associated with minor chela.
The assignment of the material to Lepidophthalmus is based on these characters: 1) typical
shape of minor chela, i.e. square propodus with long fixed finger, which is relatively high
proximally, no teeth or serration is present on occlusal margin of both fingers; 2) major chela
consisting usually of massive propodus with high dactylus, distal margin of propodus bears a
single blunt tooth below the articulation with dactylus; 3) ovoid merus in outline with tiny
meral hook positioned proximally; faint lobe positioned on the distal lower margin, which is
typical for the genus, is insufficiently preserved; 4) major cheliped carpus is distinctly shorter
than high. Occlusal margin of major cheliped fixed finger typically bears serration. No extant
of fossil congener has such armament.
21. posvetovanje slovenskih geologovGašparič & Hyžný, Abstract
4
Infraorder Gebiidea
Family Laomediidae
Jaxea kuemeli BACHMAYER, 1954 (Fig. 2.D)
A single specimen consisting of two equal chelipeds, with fragmented remains of associated
carpus. The fossil specimen represents the first report of Jaxea from Slovenia. Jaxea kuemeli
Bachmayer, 1954 was first described from the Miocene of Austria (Bachmayer, 1954) and
from lower to middle Miocene strata of Slovakia and Hungary (Hyžný, 2011).
Infraorder Brachyura
Family Retroplumidae
Retropluma n. sp. (Fig. 2.E)
Material consists of 97 mostly articulated specimens, making it the most abundant species in
the studied assemblage. Several retroplumids are described from Europe. The oldest species
are Retropluma gallica Artal, 2006 and Retropluma eocenica Via Boada, 1959 from the
Eocene layers of Spain and Italy (Beschin et al., 1996). Retropluma cf. eocenica is also
described from the Oligocene of Italy (Marangon & De Angeli, 2007). Miocene species
Retropluma borealis Fraaije, 2005 is described from Gram in Denmark as the northernmost
locality of the genus Retropluma. The youngest fossil species Reropluma craverii De Angeli,
2011 is described from the Pliocene of Italy. The Činžat material differs from the known
Retropluma species by well marked regions, strong carinas forming lateral projections, strong
outwards facing postorbital teeth, a presence of infraorbital teeth, and long distally widening
rostrum. It resembles a recent Retropluma serenei Saint Laurent, 1989, but has more
pronounced regions and carinas as well as stronger supraorbital and postorbital teeth then the
extant species.
Family Pilumnidae
Styrioplax exiguus GLAESSNER, 1928 (Fig. 2.F)
Altogether 72 specimens could be observed in various modes of preservation, some are dorso-
ventrally compressed, but some also in three-dimensional preservation. Almost all specimens
are articulated. After Glaessner’s (1928) description the material from Šentilj and Lenart was
cited as Austrian (Karasawa & Kato, 2003). The redescription (Hyžný & Schlögl, 2011)
recognizes the Slovenian origin of this material and adds additional lower Miocene localities
from the Austrian quarry Retznei and from Slovakia.
21. posvetovanje slovenskih geologovGašparič & Hyžný, Abstract
5
Family Mathildellidae
Neopilumnoplax n. sp. (Fig. 2.G)
The material consists of three specimens, including an isolated cheliped. The described
material represents the first species of the genus Neopilumnoplax in the fossil record. Several
Paleocene to Oligocene members of the Mathildellidae have been described from North
America (Karasawa et al., 2008), but no Neogene representatives of the family have been
known so far. A new species from Činžat resembles the recent Neopilumnoplax lipkeholthuisi
Tavares, 2010, but differs in front and orientation of anterolateral teeth.
Family Goneplacidae
Goneplax cf. sacci CREMA, 1859 (Fig. 2.H)
Three specimens of partially preserved carapace are assigned to the Goneplacidae and closely
resemble Goneplax sacci Crema, 1895. The specimens differ from Goneplax rhomboides
Linnaeus, 1758 (Garassino, 2012) in having more convex anterolateral margins with shorter
anterolateral teeth and wider front, similar to Goneplax sacci (Bachmayer, 1953).
References
Artal, P., Bakel, B. Van, & Castillo, J. 2006: Retropluma Gill, 1894 (Crustacea, Decapoda) from the Eocene of
the eastern Pyrenees (Spain, France). Cainozoic Research 5, pp. 6571.
Bachmayer, E. 1954: Zwei bemerkenswerte Crustaceen Funde aus dem Jungtertiar des Wiener Beckens.
Sitzungsberichte der Osterreichischen Akademie der Wissenschaften in Wien I, pp. 63-70.
Bartol, M., Mikuž, V. & Gašparič, R. in print: Nekaj primerov datiranja makrofosilov s kalcitnim
nanoplanktonom. Geološki zbornik 21.
Beschin, C., Busulini, A., De Angeli, A. & Tessier, G., 1996: Retroplumoidea (Crustacea, Brachyura) nel
Terziario del Vicentino (Italia settentrionale). Lavori - Società Veneziana di Scienze Naturali 21, pp. 83-
102.
De Angeli, A., Garassino, A. & Pasini, G., 2011: Retropluma craverii (Crema, 1895) (Crustacea, Decapoda,
Brachyura, Retroplumidae) from the Pliocene of Reggio Emilia (N Italy). Atti della Società italiana di
Scienze naturali e del Museo civico di Storia naturale in Milano 152, pp. 37-44.
Fodor, L., Jelen, B., Marton, E., Rifelj, H., Kraljič, M., Kevrič, R., Marton, P., Koroknai, B. & Baldi-Beke, M.
2002: Miocene to Quarternary deformation, stratigraphy and paleogeography in Northeastern Slovenia nad
Southwestern Hungary. Geologija45/1, pp. 103-114.
Fraaije, R., Hansen, J. & Hansen, T. 2005: Late Miocene decapod fauna from Gram, Denmark. Palaeontos 7, pp.
51-61.
21. posvetovanje slovenskih geologovGašparič & Hyžný, Abstract
6
Garassino, A., Artal, P. & Pasini, G. 2009: Jaxea nocturna Nardo, 1847 (Crustacea, Thalassinidea, Laomediidae)
from the Pliocene of Catalonia (Spain). Atti della Societa Italiana di Scienze Naturali e del Museo Civicodi
Storia Naturale di Milano 150, pp. 69-76.
Glaessner, M. F. 1928: Die Dekapodenfauna des osterreichischen Jungtertiars. Jahrbuch der Geologischen
Bundesanstalt 78, pp. 161-219.
Glaessner, M. F. 1969: Decapoda. In: Moore, R. C. (Ed.): Treatise on Invertebrate Paleontology, Pt. R4:
Geological Society of America & University of Kansas Press, pp. 400-533
Pavšič, J. & Horvat, A. 2009: Eocene, Oligocene and Miocene in Central and Eastern Slovenia. In: Pleničar, M
(Ed.): The Geology of Slovenia, Geološki zavod Slovenije, pp. 373-426.
Hyžný, M. & Schlögl, J. 2011: Revision of Jaxea kuemeli Bachmayer, 1954 (Decapoda: Gebiidea:
Laomediidae) from the Miocene of Europe, with remarks on the palaeobiogeography of the genus Jaxea
Nardo, 1847. Neues Jahrbuch für Geologie und Paläontologie Abhandlungen 260, pp. 173–184.
Jelen, B. & Rifelj, H. 2002: Stratigraphic structure of the B1 Tertiary tectonostratigraphic unit in Eastern
Slovenia. Geologija 45/1, pp. 115-138.
Karasawa, H. & Kato, H. 2003: The family Goneplacidae MacLeay, 1838 (Crustacea: Decapoda: Brachyura):
systematics, phylogeny, and fossil records. Paleontological Research 7, pp. 129–151.
Karasawa, H., Kato, H., Kase, T., Maac-Aguilar, Y., Kurihara, Y., Hayashi, H. & Hagino, K. 2008: Neogene and
Quaternary Ghost Shrimps and Crabs (Crustacea: Decapoda) from the Philippines. Bull. Natl. Mus. Nat.
Sci., Ser. C, 34, pp. 5176.
Marangon, S. & De Angeli, A. 2007: New decapod assemblage from the lower Oligocene (Rupelian) of Bacino
Ligure Piemontese (NW Italy). In: 3rd Symposium on Mesozoic and Cenozoic Decapod Crustaceans.
Museo di Storia Naturale di Milano, Memorie della Società italiana di Scienze naturali e del Museo civico di
Storia naturale di Milano, pp. 73-75.
Mikuž, V. 2003: Miocenske rakovice iz okolice Šentilja v Slovenskih Goricah. (The Miocene crabs from vicinity
Šentilj in Slovenske Gorice, Slovenia) Razprave IV. razreda SAZU 44, pp. 187–199.
Mioč, P. 1972: Tolmač za list Slovenj Gradec. Osnovna geološka karta SFRJ 1:100.000, Tvezni geološki zavod,
74 pp.
Mioč, P. 1977: Geološka zgradba Dravske doline med Dravogradom in Selnico. (Geological Structure of the
Drava Valley between Dravograd and Selnica). Geologija 20, pp. 193-230.
Ngoc-Ho, N. 2003: European and Mediterranean Thalassinidea (Crustacea, Decapoda). Zoosystema 25, pp. 439
555.
Rögl, F. 1998: Paleogeographic Considerations for the Mediterranean and Paratethys Seaways (Oligocene to
Miocene). Ann. Naturhist. Mus. Wien 99A, pp. 270-310.
Saint Laurent de, M. 1989: La nouvelle superfamille des Retroplumoidea Gill, 1894 (Decapoda, Brachyura):
systématique, affinités et évolution. In: Résultats des Campagnes Musorstom, 5. Forest J. (ed.). Mémoire du
Muséum national d’Histoire naturelle 144, pp. 103-179.
Tavares, M. & De Melo, G., 2010: A New Species of Neopilumnoplax Serene in Guinot, 1969 (Decapoda,
Brachyura, Mathildellidae) from the Southwestern Atlantic. In: Fransen et al. (eds.), Lipke Bijdeley Holthuis
Memorial Volume, Studies on Malacostraca, pp. 685-691
21. posvetovanje slovenskih geologovGašparič & Hyžný, Abstract
7
Fig. 2.A) Callianassa cf. michelottii, B) Callianassa sp., C) Lepidophthalmus n. sp., D)
Jaxea kuemeli, E) Retropluma n. sp., F) Styrioplax exiguus, G) Neopilumnoplax n. sp., H)
Goneplax cf. sacci. Scale bar in all is 10 mm.
ResearchGate has not been able to resolve any citations for this publication.
Article
Full-text available
We report two specimens of retroplumid crabs from the Pliocene of Reggio Emilia (N Italy), ascribed to Retropluma craverii (Crema, 1895), known to date only from the Pliocene of Pie- monte. The re-examination of the holotype together with the good state of preservation of the studied specimens has allowed a re-description of this species, poorly known to date.
Article
Full-text available
Six species of decapod crustacean (two macrurans, one anomuran, three brachyurans) are recognised from upper Miocene strata exposed at the Gram clay-pit, south-west Jutland, Denmark. Three new species, Retropluma borealis, Chaceon miocenicus, and Nephrops kvistgaardae, are erected; the genera Tasadia and Munida are recorded from the Danish Miocene for the first time. Abstrakt: De øvre miocaene aflejringer blotlagt i Gram Teglvaerksgrav indeholder seks arter af tibenede krebsdyr (to hummere, en anomura og tre krabber). Tre af disse, Retropluma borealis, Chaceon miocenicus og Nephrops kvistgaardae, har ikke tidligere vaeret beskrevet, mens de to slaegter Tasadia og Munida for første gang dokumenteres fra det danske Miocaen.
Article
Full-text available
Neopilumnoplax lipkeholthuisi sp. nov. is described from the southwestern Atlantic. The new species can be easily separated from its congeners by a suite of carapace and appendage characters. RÉSUMÉ Neopilumnoplax lipkeholthuisi sp. nov. est décrite de l'Atlantique sud-occidental. La nou-velle espèce se sépare aisement de ses congénères par divers caractères de la carapace et des appendices.
Article
Full-text available
A phylogenetic analysis of 14 genera of the family Goneplacidae MacLeay (Decapoda: Brachyura: Xanthoidea) is presented based upon 45 adult morphological characters. Two most-parsimonious trees were obtained (length = 87, CI = 0.6667, RI = 0.8242, RC = 0.5495). The present analysis suggests that the Goneplacidae is divided into six subfamilies: Carinocarcinoidinae subfam. nov., Chasmocarcininae Serene, Euryplacinae Stimpson, Goneplacinae MacLeay, Mathildellinae subfam. nov., and Trogloplacinae Guinot. The Carcinoplacinae H. Milne Edwards is synonymised with the Goneplacinae. The family and six subfami-lies are defined or redefined based upon the phylogenetic analysis. Within the Goneplacidae, the Trogloplacinae and Chasmocarcininae are sister groups nested as the most derived clade, followed by the Carinocarcinoidinae, Goneplacinae, Euryplacinae, and the most basal Mathildellinae. Our analysis supports recognition of the family Pseudoziidae Alcock by Ng and Liao and suggests that it is the sister to the Eriphiidae MacLeay. A reexamination of fossil records of the Goneplacidae shows that 62 species, 20 genera, and five subfamilies are recognized as fossils. A new monotypic genus Viaplax (Euryplacinae) is erected for Pilumnoplax urpiniana Via. Chlinocephalus Ristori and Gillcarcinus Collins and Morris are moved to the Goneplacidae. Paleopsopheticus Hu and Tao is synonymised with Psopheticus Wood-Mason. Glaessneria Takeda and Miyake is here the junior synonym of Goneplax. Eleven extinct genera previously assigned to the Goneplacidae are not referred to any subfamilies and are transferred out of the Goneplacidae. New combi-nations include: Carcinoplax proavita (Glaessner), Goneplax arenicola (Glaessner), Euphylax zariquieri (Via) (Portunidae Rafinesque), and Psopheticus shujienae (Hu and Tao).
Article
Full-text available
High inconsistency and incoherence in the stratigraphy of the Slovenian upper Paleogene and lower Miocene have remained unsolved in the past 150 years. To solve the problem, we tried to rigorously conduct the authentic Galilei’s scientific method. Steps of logical and empirical verification confirmed the existence of the posited B1 Tertiary tectonostratigraphic unit, and a general chronostratigraphic model of new positional relationships of lithologic units resulted from rather good biochronostratigraphic resolution achieved by nannoplankton and planktonic foraminifera biostratigraphy. The application of principles of newly developed fields in science helped us to avoid errors in transmission of messages (to reduce noise) from the source (rock) to the concept formation, which had been done previously. This in turn has strongly reduced inconsistency and incoherence (high information entropy = uncertainty). The released amount of information enabled us to answer also questions that reached beyond the original difficulty, e.g.: is the tectonostratigraphic structure of eastern Slovenia a manifestation of plate tectonics processes, and of which ones, are theories of continental escape in the Alps and associated dissection and offset of the formerly uniform Slovenian-Hungarian Paleogene basin tenable or not, are then there in the B1 stratigraphic equivalents of the Hungarian Paleogene basin formations, where are the important Eocene / Oligocene, Paleogene / Neogene, Rupelian / Chattian and Kiscellian / Egerian boundaries in Slovenia, and is there a continuation of the B1 in Croatia and in the Mid-Hungarian tectonic zone?
Article
All genera and species from Europe and the Mediterranean are diagnosed or redescribed, differentiating characters are illustrated and an identification key is provided. A review of literature and biological information is included, and a classification, with two new genera, is proposed. The superfamily Axioidea comprises the Axiidae, with Axius stirhynchus, Calocarides coronatus, Levantocaris hornungae; and the Calocarididae with Calastacus laevis and Calocaris macandreae. The Callianassoidea include the Callianassidae, Ctenochelidae, Laomediidae and Upogebiidae. The Callianassidae contain three subfamilies. The Callianassinae have three species placed in Callianassa: C. acanthura, C. subterranea and C. truncata; three other species are assigned to a new genus, Pestarella n. gen.: P. candida n. comb., P. tyrrhena n. comb. and P. whitei n. comb. Pestarella n. gen. species have an operculiform Mxp3, a telson rounded in posterior half, and no Plp1-2 in male. The little known species Calliapagurops charcoti is placed in the Callichirinae. The Eucalliacinae contain two species: Calliax lobata and Calliaxina punica n. comb., type species of a new genus, Calliaxina n. gen. Species of Calliaxina n. gen. possess a rostrum with pointed tip, an operculiform Mxp3 with exopod,, the P1 equal and similar, and Plp1-2 with appendix interna in both male and female. The Ctenochelidae have one subfamily, Gourretinae with Gourrretia denticulata. The Laomediidae are re resented by one species, Jaxea nocturna, the Upogebiidae by seven species: Gebiacantha talismani, Upogebia deltaura, U. mediterranea, U. nitida, U. pusilla, U. stellata and U. tipica.