Synopsis of fossil fish fauna from the Hermanowa locality (Rupelian; Central Paratethys; Poland): current state of knowledge
Swiss Journal of Geosciences volume 109, pages 429–443 (2016)
This publication represents the first comprehensive review of the currently known palaeoichthyological diversity of the Hermanowa locality (Poland). Specimens were collected from a single outcrop belonging to the single IPM zone (IPM2-T according to the presence of the index taxon Trachinus minutus). The assemblage is composed of two elasmobranch taxa and 22 taxa of teleosts. Overwhelming part of the assemblage is represented by teleosts; elasmobranchs are present in less than 0.5 %, with one new taxon for the Polish Carpathians (Physogaleus latus). The meso-pelagic and bathy-pelagic fishes are missing; dominant part of the assemblage is composed of the neritic taxa. Developmental stages of some taxa were recognized and relatively common throughout the whole section. The assemblage is briefly discussed.
Oligocene–Miocene fishes of the Polish Carpathians have been intensively studied since the second half of the twentieth century by Anna Jerzmańska and her coworkers (e.g., Jerzmańska 1960, 1967, 1968, 1974, 1979; Jerzmańska and Kotlarczyk 1975, 1976; Jerzmańska and Świdnicka 2003; Kotlarczyk et al. 2006; for a complete overview of the references, see the last publication). Rich localities, such as Jamna Dolna provided important documentations in extraordinary detail (in a quantitative and qualitative sense) of this fauna, which inhabited the Central Paratethys region during the Oligocene to Early Miocene. Over time, an enormous collection of fish specimens from the region was assembled (today housed in Wroclaw University), which, together with sedimentary and lithostratigraphic data, also allow the elaboration of an ichthyostratigraphical concept for the area, i.e., IPM zones (Kotlarczyk and Jerzmańska 1976; Kotlarczyk et al. 2006). Although these fish faunas have been intensively studied for a long time, the whole region is still attractive for palaeoichthyological exploration today.
The Hermanowa locality is located in southeastern Poland, about 12 km south of the center of Rzeszow (Fig. 1). Kotlarczyk et al. (2006) mentioned two places with the name Hermanowa: Hermanowa and Hermanowa Kamieniec (the latter place with two exposures; according to the original publication abbreviated as HE, HK1 and HK2, respectively). Nevertheless, the Hermanowa locality (HE sensu Kotlarczyk et al. 2006) is synonymous with the place described herein. Kotlarczyk et al. (2006) also briefly sketched the taxonomic composition of the assemblage, but this was based on a limited number of specimens. The locality was more recently intensively sampled from 2005 to 2015, and this collection comprises several hundred fish remains.
The primary purpose of this paper is to provide an overview of the fish taxa of the Hermanowa locality, with an accompanying brief discussion of the fauna as a whole.
Material and locality
The material is housed at the University of Rzeszow (UR/KBŚ), Institute of Systematics and Evolution of Animals, Polish Academy of Sciences, Krakow (Pi-F), and the National Museum in Prague (NMP). The standard length (SL) abbreviation is used elsewhere in the text. Taxa synonomies are not included for all taxa due to space limitations (they may be found in the references). Photographs were taken with a Nikon D3100 camera, and a Canon EOS 1000D associated with a binocular Leica MZ6 stereomicroscope.
The material consists of natural moulds of skeletons in sediment (the original bone tissue was destroyed during the fossilization process); when bones are preserved (very rarely), these are limonitized. Soft tissue impressions (e.g., alimentary canal or body pigmentation) are rarely recognizable. Specimens were left unprepared, or were lightly prepared using small scalpels or needles.
The specimens were collected from a single outcrop (Fig. 2; GPS lat 49.934266; long 22.019500), located in the Hermanowa village. The presence of the index species Trachinus minutus (distributed in all parts of the profile) allows the assignment of the locality to the Trachinus event of the IPM2 zone (for the palaeoecologic interpretation of this event see Kotlarczyk et al. 2006). This biostratigraphic restriction allows the assignment of this section to the Rupelian age (Early Oligocene) and more preciously to the NP23 calcareous nannoplankton zone (see Kotlarczyk et al. 2006: fig. 33).
The fish fauna is well distributed in all parts of the profile, but seems to be more abundant in some sections (these are marked by a fish symbol in Fig. 2). Some taxa seem to be limited to only particular sections; this is mentioned in the descriptive part of the text where applicable. The upper part of the profile is less accessible for sampling.
Class Chondrichthyes Goodrich, 1909
Subclass Elasmobranchii Bonaparte, 1832
Order Lamniformes Berg, 1940
Family Cetorhinidae Gill, 1862
Genus Keasius Welton, 2013
Keasius parvus (Leriche, 1908)
Synonymy Refer to Reinecke et al. (2015).
Material examined Two specimens—UR/KBŚ/444 (part and counterpart), UR/KBŚ/445.
Description Basking sharks are represented by two specimens of isolated gill rakers (branchiospines) in the studied material. The typical sickle-shaped base is connected with a long, incompletely preserved filament.
Remarks Fossil specimens of these sharks were originally classified in an extinct species of the recent genus Cetorhinus, but Welton (2013) erected a new genus to house the extinct species. The specimens are well known (including rare, mostly complete individuals; Hovestadt and Hovestadt-Euler 2012) from the Eocene, Oligocene and Miocene of the Paratethys area, and detailed study of the gill rakers and teeth show an unexpected diversity of species in the genus Keasius (Reinecke et al. 2015).
The presence of this species in the locality is problematic. Lithology of the slabs is atypical for the locality, and has not been observed directly in the profile (specimens were found in the rubble under the profile wall).
Order Carcharhiniformes Compagno, 1973
Family Carcharhinidae Jordan & Evermann, 1896
Genus Physogaleus Capetta, 1980
Physogaleus latus (Storms, 1894)
Figure 3a, b
Synonymy Refer to Ciobanu (2002).
Material examined Pi-F/MP/10/1483/08 (counterpart Pi-F/MP/11/1483/08).
Description The single specimen (an upper lateral tooth) shows a wide root, with well-developed nutritive groove; short apex, inclined distally; tip not exposed; four wide cusplets in the distal heel; mesial cutting edge; crown tongue developed in transition from crown to root, ventrally borded by vertical ridges; root in lingual view bears well developed lingual protuberance; basal edge of root bears numerous foramina.
Remarks The specimen was discovered in the lower part of the section. The occurrence of the species was recorded from the Early Oligocene of Belgium (Leriche 1910; Bor 1980), Paris Basin (Leriche 1910), Hungary (Weiler 1938), France (Pharisat 1991, 1998; Pharisat and Micklich 1998), Germany (Micklich and Parin 1996; Pharisat and Micklich 1998), and Romania (Ciobanu 2002). This species has a temporal distribution through the Early Miocene (for details see Cappetta 2012).
Division Teleostei sensu Patterson & Rosen, 1977
Order Clupeiformes Bleeker, 1859
Family Clupeidae Bonaparte, 1831
Genus Sardinella Valenciennes, 1847
Sardinella cf. S. sardinites (Heckel, 1850)
Synonymy Synonymy of S. sardinites refer to Přikryl (2013).
Material examined 144 specimens—UR/KBŚ/ 1–4, 8, 13, 17, 25, 68, 77, 79–82, 84–88, 91, 93, 94, 96, 101, 102, 104, 105, 109, 111, 113, 114, 117–119, 124–126, 129–132, 134–136, 140, 149, 153, 154, 160, 163, 179, 189–192, 260, 261, 281, 282, 288, 289, 300, 311, 322, 326–328, 330, 342, 347, 359, 361, 364, 368, 372, 375, 384, 390, 407, 413, 418, 421, 424, 425, 427, 429, 439, 440, 446, 454, 457, 461, 466, 482, 485, 486, 488, 490, 494, 499, 501, 502, 531, 540, 543, 545, 546, 551, 561, 614, 617, 620, 625, Pi-F/MP/30, 40/1485/08, Pi-F/MP/1, 8, 11, 17, 19, 20, 26/1591/11, Pi-F/MP/2, 3/1592/11, Pi-F/MP/4, 7, 10, 11, 14/1510/08, Pi-F/MP/8, 10/1539/08, Pi-F/MP/31, 55, 67, 98, 99, 101, 102, 104, 128, 132, 134/1598/11 (some of them with counterparts).
Description Small fish with laterally compressed body. Head triangular; head length slightly less than three times in standard length. Mouth terminal, dorsally oriented. Lower jaw joint in front of anterior-most margin of orbit. Two supramaxillae. Orbit large, with parasphenoid exposed in ventral part. Prootic bulla seems to be larger than pterotic bulla. Opercle smooth, with no obvious ornamentation. Vertebral column consists of 42–45 preural vertebrae (but some specimens show fewer, about 40); about 21 pairs of ribs; three series of intermuscular bones. Dorsal fin located in middle of body, composed of 15–17 (in some specimens possibly 19) fin rays. Nine or ten supraneural bones are recognizable. First dorsal fin pterygiophore is forked. The anal fin is shifted posteriorly and consists of 18 fin rays; the last two shifted to a more posterior position. Pectoral fin consists of 16–19 rays. Pelvic fins start at level of posterior part of dorsal fin, and consist of eight or nine rays. The series of abdominal scutes is developed anteriorly and posteriorly to the pelvic fin. Caudal fin deeply forked. Body covered by cycloid scales.
Remarks Clupeids from the Polish Carpathians were traditionally classified as Clupea sardinites (Jerzmańska 1968; Szymczyk 1978), but Daniltshenko (1980) and later also Grande (1985) suggested transferring this species to the genus Sardinella. The species has a large geographic distribution (for details see Grande 1985; and Carnevale et al. 2006) with a stratigraphic range from the Oligocene to the Middle Miocene. Despite the great need for a complete revision of many fossil clupeids, we retain the traditional classification scheme, but due to our specimens showing somewhat greater variability (especially in numbers of vertebrae) than specimens described by Jerzmańska (1968), specimens are classified as Sardinella cf. S. sardinites. The species is one of the most commonly found in different ontogenetic stages at the locality, including poorly ossified larvae, juveniles and (sub-) adults. The specimens are distributed throughout the section.
Family Clupeidae Bonaparte, 1831
Genus and species indeterminate
Material examined Pi-F/MP/171/1648/15 (part and counterpart).
Description A single incomplete specimen (with estimated SL about 150 mm) shows important differences the clupeid taxon described above, such as the lower jaw joint situated under the center of the orbit (or slightly posteriorly); the opercle bears well-developed postero-ventral striations; pelvic fin with seven or eight rays; pelvic fins start at the level of the anterior portion of the dorsal fin; abdominal scutes are more strongly developed. It is similar to the previous form in the number of pectoral fin rays (around 16), and cycloid scales.
Remarks Although this specimen is far from complete, it is definitely a different clupeid taxon than Sardinella cf. S. sardinites (described above), with possible affinities to several clupeids, including the genus Alosa (the taxon was mentioned from the Polish Carpathians under a younger synonym Pomolobus by Jerzmańska 1968). For a definitive taxonomic placement, better preserved specimens are needed.
Order Osmeriformes sensu Nolf & Dockery, 1990
Family Argentinidae Bonaparte, 1846
Genus Glossanodon Guichenot, 1867
“Glossanodon” musceli (Paucă, 1929)
Figure 3 g, h
Synonymy Refer to Přikryl (2013).
Material examined More than three hundred specimens (not listed completely herein)—e.g., UR/KBŚ/9, 11, 12, 14–16, 20–24, 40–55, 73 and many others (some of them with counterparts).
Description Small, slightly elongated fish. Head tear drop-shaped in lateral view, with terminal mouth; lower jaw joint at level of anterior margin of orbit; maxilla slightly bent with flattened posterior projection rounded antero-ventrally; preopercle with rami of approximately same length and two short ridges at angle of bone. About seven branchiostegal rays. Posttemporal articulates with supracleithrum in a 90° angle. Supracleithrum aligned vertically with cleithrum. Vertebral column consists of 45–47 vertebrae (abdominal vertebrae 24–26; caudal vertebrae 20–22) with 23 or 24 pairs of ribs. Intermuscular bones seem to be present. Left and right neural spines of anterior part of vertebral column apparently not fused in midline. Dorsal fin composed of 10–12 rays, located approximately mid-body. Anal fin shifted posteriorly (starts about four vertebrae posterior to first caudal vertebra), composed of 13 (or slightly more) rays. Pectoral fins in fairly ventral position, composed of 16 to 18 fin rays. Pelvic fins midway between pectoral and anal fins, just under origin of dorsal fin (or slightly anteriorly). Pelvic fins composed of eight to ten rays. Caudal fin deeply forked, composed of 10 + 9 principal rays.
Remarks The specimens are fairly abundant and represent different ontogenetic stages, almost throughout the stratigraphic section of the locality. The species is well distributed in Oligocene localities of the Central and Eastern Paratethys (Paucă 1929, 1934; Daniltshenko 1960; Jerzmańska 1967; Prokofiev 2005b; Gregorová 2011), but missing at the coeval localities of the Rhine valley (Pharisat 1991; Micklich and Parin 1996; Micklich 1998; Pharisat and Micklich 1998), Alpine foredeep (Wettstein 1886; von Rath 1859) and Iran (Arambourg 1967; the locality is of greater stratigraphic range now, see Afsari et al. 2014). The morphology and osteology of this species was described by Paucă (1929, 1934), Daniltshenko (1960), Jerzmańska (1967), and newly revised also by Prokofiev (2005b), who suggested the erection of a new genus Austromallotus to accommodate a part of the fossil material. We did not observe features considered diagnostic by Prokofiev (2005b) for the genus Austromallotus in our specimens, and thus retain the traditional classification to the genus Glossanodon.
Order Aulopiformes Rosen, 1973
Family Paralepididae Bonaparte, 1832
Subfamily Holosteinae Prokofiev, 2005
Genus Holosteus Agassiz, 1839
Material examined Three specimens—UR/KBŚ/251, 252, and probably also 265 (some of them with counterparts).
Description None of the specimens are complete (head, caudal portion and some fins are missing), but the remains belong to an elongate fish with numerous vertebrae (more than 70 preserved vertebrae, precise number unknown). Around 45 ribs; two series of intermuscular bones recognizable. Dorsal and anal fins shifted posteriorly; predorsal length greater than preanal length. Dorsal fin consists of more than 15 rays. Anal fin not preserved completely, but preserved rays suggest presence of more rays than found in dorsal fin. Pectoral fin shifted ventrally, composed of more than 15 rays. Pelvic fin has wide base; precise number of fin rays is not clear.
Remarks The specimens are restricted to the layers “H33” and “R”. The overall appearance of the specimens suggest an affinity to the family Paralepididae, and they can be placed in the Holosteinae subfamily on the basis of a greater predorsal than preanal distance (other features used by Prokofiev 2005a for defining this subfamily are not preserved). The subfamily comprises one single genus, with one early Eocene species from Monte Bolca (Carnevale et al. 2014) and probably one Oligocene species [Prokofiev 2005a; although some specimens from the Romanian Carpathians were classified in a separate species H. fieniensis by Constantin (2001), their separate taxonomic status should be verified].
Order Gadiformes sensu Endo, 2003
Family Moridae Goode & Bean, 1896
Genus Eophycis Jerzmańska, 1968
Eophycis jamnensis Jerzmańska, 1968
1968 Eophycis jamnensis n. sp.—Jerzmańska: 413, text-fig. 8, pl. III, fig. 3.
2015 Eophycis jamnensis Jerzmańska, 1968—Přikryl: 626, figs. 1–10.
Material examined 45 specimens—UR/KBŚ/95, 97, 180, 183, 185, 201, 202, 204, 205, 207, 208, 213, 270, 271, 276, 285–287, 293–296, 302, 303, 308, 309, 312, 318, 414, 419, 471, 510, 511, 523, 530, 554, Pi-F/MP/23/1572/10, Pi-F/MP/4, 7, 9, 11–13/1592/11, NMP Tv 1002, 1003 (some of them with counterparts).
Remarks The species was morphologically described in detail by Přikryl (2015a). It should be noted that part of the undescribed uncatalogued material also studied (superficially similar to E. jamnensis) suggests the probable presence of another form, provisionally classified as Gadiformes indet., that differs from E. jamnensis in vertebral and fin ray formulas, and arrangement of fins. Nevertheless, until better preserved and more numerous specimens are collected, we are not able to clarify the relationships of these two taxa.
Family Merlucciidae Gill, 1884
Genus Palaeogadus von Rath, 1859
Material examined Nine specimens—UR/KBŚ/6, 29, 577, 578, Pi-F/MP/16/1572/10, Pi-F/MP/25, 26/1598/11, Pi-F/MP/12, 16/1591/11 (some of them with counterparts).
Description Slightly laterally compressed fish with moderately elongate body. Head triangular, with terminal mouth; lower jaw joint at level of posterior margin of orbit; premaxilla and dentary with well-developed teeth. Vertebral column composed of 44–45 vertebrae (23 abdominal; 21–22 caudal). Neural spines of anterior abdominal vertebrae enlarged; neural spine of first vertebra not fused with occipital part of skull. Abdominal vertebrae bear well-developed triangular parapophyses (wider anteriorly, tapered posteriorly); posterior margin of each parapophysis straight, anterior margin slightly sigmoidal to convex (shape trapezoidal in some cases); neighboring parapophyses not in contact with each other. Ribs relatively short. Epicentrals present. At least one supraneural seems to be present, just in front of first dorsal fin. First dorsal fin short, composed of 11 rays supported by 10 pterygiophores. Supraneural bone, and first and second pterygiophores housed between first and second neural spine. Second dorsal fin shifted very slightly posteriorly, composed of 28–30 rays. Anal fin starts at approximately same level as second dorsal fin, elongate and composed of 33–35 rays. About 16 anterior pterygiophores of anal fin in front of first haemal spine. Caudal fin rounded. X and Y accessory bones not present. Pectoral fin composed of 14 rays. Pelvic fins positioned anteriorly under pectoral girdle, composed of five rays. Body covered by cycloid scales.
Remarks The specimens approximately fit the characters of Palaeogadus simionescui, including the morphology of the parapophyses. Due to the currently unexplained variability of some features, and the need for revision of the Palaeogadus group, we classify our specimens as Palaeogadus sp.
Order Beloniformes Berg, 1937
Family Hemiramphidae Gill, 1859
Genus and species indeterminate
Material examined Two specimens—UR/KBŚ/298 (part and counterpart); Pi-F/MP/54/1485/08.
Description Incomplete fragments of two individuals with head and anterior part of body (the following description is related to better preserved specimen UR/KBŚ/298). Head tear drop-shaped. Frontals wide, roughly rectangular. Upper jaw shortened, lower jaw prolonged (although not preserved completely – rostrum is broken off). Lower jaw joint at level of anterior half of orbit. Orbit oval, with parasphenoid running through middle. Preopercle is “L” shaped, with horizontal limb slightly longer than vertical limb. 21 vertebrae preserved, in anterior part with ribs, but preservation is not perfect. Slightly elongated pectoral fins preserved in position perpendicular to body axis, composed of seven fin rays.
Remarks The specimens are incomplete, but general features of the body shape and elongated jaw allow us to classify the specimen to the order Beloniformes. Jerzmańska (1968) described beloniform fish from the Polish Carpathians, and classified them in the genus Hemiramphus, with a new species H. jerzyi (Jerzmańska 1985). Later, the species was transferred to the genus Hyporhamphus (see Bannikov 2010).
Order Gasterosteiformes sensu Pietsch, 1978
Family Syngnathidae Bonaparte, 1832
Genus and species indeterminate
Material examined Six specimens—UR/KBŚ/584, 588–590, Pi-F/MP/1/1510/08, Pi-F/MP/1/1593/11 (all of them with counterparts).
Description Specimens are small individuals, one is a sub-adult. Head length is about one tenth of standard length. Snout length is around half of head length. Abdominal part of body is slightly more than half of standard length. Ventrally exposed opercle shows radially arranged series of ridges. Scutes arranged in less than 40 rings. No spines recognizable on surface of scutes. No fins preserved except caudal fin. Caudal fin preserves less than 10 rays.
Remarks Syngnathids were described from different parts of the Paratethys region and classified in several taxa, with the most common representative being Syngnathus incompletus originally described from Romania (Cosmovici 1887). The more diverse Oligocene syngnathid assemblage was described from the Frauenweiler locality (Rhine valley; Micklich and Parin 1996) with three genera. The specimens are still under more detailed study and therefore classified within open nomenclature.
Genus Hipposyngnathus Daniltshenko, 1960
Hipposyngnathus neriticus Jerzmańska, 1968
1968 Hipposyngnathus neriticus n. sp.—Jerzmańska: 437, text-figs. 15A, 16, pl. VII, figs. 2, 3a.
2011 Hipposyngnathus neriticus Jerzmańska, 1968—Přikryl et al.: 561, figs. 2–4.
Material examined Five specimens—UR/KBŚ/585–587, Pi-F/MP/4, 5/1572/10 (some of them with counterparts).
Remarks The species was morphologically described in detail by Přikryl et al. (2011). The specimens are distributed in the lowermost part of the profile (H5 layer).
Family Centriscidae Rafinesque, 1810
Genus and species indeterminate
Material examined Four specimens—UR/KBŚ/200, 203, Pi-F/MP/8/1592/11, Pi-F/MP/172/1648/15 (some of them with counterparts).
Description Small specimens, incomplete, greatly shortened body, with elongated snout. Radially ornamented opercle; well-developed dorsal and ventral scutes. No fins recognizable.
Remarks The overall appearance of the specimens allow us to classify them as centriscids, but the specimens are still under more detailed study, and therefore are not classified more precisely (for details and review of up to date literature see Parin and Micklich 1996).
Order Perciformes Bleeker, 1859
Family Priacanthidae Gill, 1872
Genus Priacanthus Oken, 1817
Priacanthus longispinus Lednev, 1914
Figure 4b, c
Synonymy Refer to Bannikov (2010).
Material examined Two specimens—UR/KBŚ/572, Pi-F/MP/19/1510/08 (both of them with counterpart).
Description Fish with relatively deep body; maximum body depth about one third standard length, similar to head length. Head approximately as deep as long, with large eye. Lower jaw joint at level of center of orbit. Preopercle bears serrations posteriorly; ventral margin with long spine developed at angle of bone. Opercle bears two spines at postero-dorsal margin of bone. Vertebral column composed of ten abdominal and 13 caudal vertebrae. Ribs developed on seven precaudal vertebrae. Epipleurals present. Single dorsal fin composed of 10 spines and 11 rays. No supraneurals observed. Anal fin composed of three spines, and 10 or 11 rays. Pectoral fins relatively short, with wide base, about 15 fin rays. Pectoral girdle has robust cleithrum, with spine developed at postero-dorsal margin. Single postcleithrum. Pelvic fins under pectoral fins, composed of one spine and five soft rays. Caudal fin and supporting skeleton not preserved in any studied specimens. Surface of body covered by modified cycloid scales (spinoid scales according to Roberts 1993), with spines at posterior margin. Lateral line position not clear.
Remarks Oligocene priacanthids are well known from many localities in all parts of the Paratethys realm (more than three species were described, traditionally classified in the genus Priacanthus or Pristigenys). These localities include sites in the Alpine foredeep (Wettstein 1886), Rhine valley (Pharisat 1991; Micklich and Parin 1996; Pharisat and Micklich 1998), Carpathians (Kotlarczyk et al. 2006) and Caucasus (Daniltshenko 1960; Bannikov 2010; Prokofiev 2013). It is probable that some of the poorly preserved specimens from the Hermanowa locality (classified as a Percoidei indet.) also belong to priacanthids.
Family Repropcidae Bannikov, 1991
Genus Repropca Bannikov, 1991
Repropca sabbai (Paucă, 1929)
1929 Properca sabbae n. sp.—Paucă: 117.
1934 Properca sabbai Paucă—Paucă: 624, pl. III, fig. 5.
1968 Properca sabbai Paucă, 1929—Jerzmańska: 446, text-fig. 18, pl. VI, fig. 2.
1991 Properca sabbai Pauca 1929—Pharisat: 41, figs. 30, 31.
Material examined UR/KBŚ/236 (part and counterpart).
Description: Small fish (ca. 25 mm SL) with spindle-shaped body. Head length less than one-third of SL; orbit diameter about one third of head length; preorbital part of head bigger than postorbital part. Head triangular, with terminal mouth and lower jaw joint at level of center of orbit. Teeth recognizable on premaxilla and dentary. Preopercle bears six spines at ventral margin of bone, posterior spine is the largest and oriented posteriorly. Eight or nine branchiostegal rays observed. Vertebral column consists of 11 or 12 abdominal and 18 caudal vertebrae. Caudal skeleton not preserved sufficiently. Eight pairs of ribs; epipleurals recognizable. Single dorsal fin starts just behind head, contains 12 spines (first spine very short, third spine longest) and 13 soft rays. Two supraneurals. Anal fin consists of three spines and seven soft rays. Pectoral fins start at ventro-lateral flank of body, closely behind head. Fin consists of 14 relatively short rays. Cleithrum robust, dorsally oriented spine in postero-dorsal margin. Pelvic fins ventral to pectoral fins, composed of one spine (strongly elongated) and probably five soft rays. Surface of body covered by small cycloid scales.
Remarks The repropcids were described from localities in the Romanian and Polish Carpathians (Paucă 1929, 1934; Jerzmańska 1968, respectively), Rhine valley (Pharisat 1991; Micklich and Parin 1996; Micklich 1998; Pharisat and Micklich 1998), and Caucasus (Bannikov 1991, 2010; Prokofiev 2013).
Family Carangidae Rafinesque, 1815
Genus and species indeterminate
Material examined Single specimen—UR/KBŚ/571 (part and counterpart).
Description Only one, severely fragmented (and poorly preserved) specimen that lacks skull and posterior-most part of body (estimated SL is about 100 mm). Body relatively deep, with eight preserved abdominal and 11–12 preserved caudal vertebrae. Anal fin has long base, first pterygiophore (with anteriorly enlarged ventral portion) bears two short bulky spines, and 22 rays. Dorsal fin composed of seven or eight preserved spines, and 22 rays.
Remarks The specimen is classified within Carangidae, but a more precise classification is still under study.
Percoidei incertae familiae
Genus Oliganodon Bannikov, 2010
Oliganodon budensis (Heckel, 1856)
Synonymy Refer to Bannikov (2010).
Material examined 36 specimens—UR/KBŚ/ 45, 122, 237, 242, 243, 253, 254, 258, 259, 263, 266, 267, 273, 310, 313, 314, 321, 355, 367, 397, 400, 403, 404, 428, 458, 517, 548, 574, 593, 594, Pi-F/MP/18/1592/11, Pi-F/MP/20/1510/08, Pi-F/MP/21/1510/08, Pi-F/MP/15/1592/11, Pi-F/MP/19/1592/11, Pi-F/MP/10/1591/11 (some of them with counterparts).
Description Small to medium sized fish. Premaxilla and dentary bear teeth. Teeth around premaxillary symphysis slightly enlarged. Lower jaw joint at level of posterior margin of orbit. Preopercle bears fine serrations at postero-ventral margin of bone. Opercle has two spines at postero-dorsal corner of bone. Vertebral column composed of 24 vertebrae (10 abdominal and 14 caudal). Abdominal vertebrae bear ribs and epipleurals. Three supraneurals present. Dorsal fin composed of 10 spines and 10 rays. Anal fin composed of three spines and eight (in several cases nine) rays. Pectoral fins composed of 16–17 rays; posterior tips of longest rays can reach level of origin of anal fin. Pelvic fins have one spine and five rays, positioned anteriorly at level of pectoral fins. Body covered by ctenoid scales, some scales in head region (especially in smaller individuals) seem to be cycloid.
Remarks This percoid is common in many Paratethys localities (for review of the principal literature, see Bannikov 2010: 86), and the material should be revised as a whole for a more detailed understanding of this taxon. Specimen Pi-F/MP/19/1592/11 is also tentatively assigned to this species, as it fits the characteristics well, with the notable deviation of 15 caudal vertebrae.
Family Ammodytidae Bonaparte, 1846
Genus and species indeterminate
Material examined Four specimens—UR/KBŚ/ 245–249 (some of them with counterparts).
Description Specimens not well preserved, but short head with terminal mouth observable (lower jaw slightly protruding past upper jaw); small eye; elongate body; pelvic fins absent; vertebral column composed of about 60 vertebrae; caudal fin deeply forked.
Remarks The specimens are limited to the “R” section of the profile. The specimens are classified within the family Ammodytidae, but better preserved specimens are needed for a more precise determination. Only one species, Ammodytes antipai, was described from the Oligocene of the Paratethys area of the Carpathians (Paucă 1929, 1934; Jerzmańska 1968), and Caucasus (Daniltschenko 1960; Bannikov 2010).
Family Trachinidae Risso, 1826
Genus Trachinus Linnaeus, 1758
Trachinus minutus (Jonet, 1958)
Synonymy Refer to Přikryl (2009).
Material examined 45 specimens—UR/KBŚ/115, 121, 186, 206, 279, 280, 291, 292, 299, 307, 319, 320, 358, 476, 477, 478, 480, 564–570, 611, Pi-F/MP/45/1485/08, Pi-F/MP/5, 9/1510/08, Pi-F/MP/4, 6–12, 14, 17–22/1572/10, Pi-F/MP/60/1598/11, NMP Tv 1001 (some of them with counterpart).
Remarks The species was described in the detail by Přikryl (2015b).
Family Caproidae Lowe, 1843
Genus Capros Lacepède, 1802
Capros rhenanus (Weiler, 1920)
Synonymy Refer to Baciu et al. (2005).
Material examined Two specimens—Pi-F/MP/5/1592/11 (part and counterpart; the following description is related with this specimen), UR/KBŚ/269 (less complete, but clearly belonging to the same species).
Description Small fish with convex dorsal and ventral body margins. Body depth less than one half of SL. Suspensorium, visceral part of cranium and parts of some fins missing. Supraoccipital crest well developed, with thickened anterior and concave posterior margin. Skull roof bones ornamented by radially arranged ridges. Supraoccipital crest reaches anteriorly past level of posterior-most orbit. No supraneurals. Base of spiny dorsal fin approximately same length as base of soft rayed dorsal fin. Vertebral column consists of 23 vertebrae (10 + 13). Ribs present at third to tenth abdominal vertebrae. First dorsal fin not completely preserved: one spine associated with the first pterygiophore (therefore the first one and supernumerary), was lost, the longest spine (on the second pterygiophore) is therefore the third one, and another five spines are recognizable. Spine associated with sixth pterygiophore not preserved. Total count of spines in dorsal fin therefore should be nine. Soft rays not preserved, but number of pterygiophores suggests that about 16 or 17 were present. Seventh interneural space vacant (in the sense of Birdsong et al. 1980). Anal fin bears three spines (first is longest); soft rays not sufficiently preserved, but it is possible to estimate about 18 soft rays (on the basis of their pterygiophores). Caudal skeleton and fin not preserved sufficiently to provide usable information.
Remarks Fossil caproids (including all up to date literature), their systematics, relationship and record were fully revised by Baciu et al. (2005), with one interesting new addition to the Polish fauna published recently by Bieńkowska-Wasiluk and Bonde (2015).
Capros cf. C. caprosoides (Cosmovici, 1887)
Figure 4 g
Synonymy Synonymy of C. caprosoides refer to Baciu et al. (2005).
Material examined Single specimen—UR/KBŚ/278 (part and counterpart).
Description Small, almost completely preserved deep-bodied fish. Head length slightly less than half of SL. Mouth terminal; jaw joint at level of anterior portion of orbit. Orbit large; preorbital distance smaller than orbit. Supraoccipital crest starts above posterior portion of orbit. Skull roof ornamented by small tubercles. Preopercle bears fine spines at ventral margin of bone; size of spines increases at angle of preopercle. Strong spine-like postcleithrum. Vertebral column composed of 22 vertebrae (10 + 12). Thin ribs recognizable only in posterior part of abdominal cavity. Dorsal fin preserves only spinous part, with nine spines (first is shortest and in supernumerary association with first pterygiophore; second and third spines approximately the same length, but second one is more robust; other spines decrease in length posteriorly). Pterygiophores accommodated one by one in interneural spaces (in the sense of Birdsong et al. 1980), with exception of seventh interneural space that is vacant. Anal fin incompletely preserved, only bases of three spines recognizable. Pectoral fins not recognizable. Pelvic fins shifted anteriorly, but only proximal parts of spines are preserved. Caudal fin insufficiently preserved, but 13 caudal fin rays recognizable.
Remarks The general description, anatomy and meristic features fit relatively well with those of Capros caprosoides (for details see Baciu et al. 2005), but some features seem to be slightly different (second and third dorsal spines are approximately same long, while third dorsal spine should be longest in C. caprosoides) or are not completely preserved (uncertainty in numbers of the soft rays in unpaired and paired fins). The specimen is thus classified as Capros cf. C. caprosoides.
Family Scombridae Rafinesque, 1815
Genus and species indeterminate
Material examined Two specimens—UR/KBŚ/277, 612 (both of them with counterpart).
Description Both specimens consist of incomplete fragments (following description is related to specimen UR/KBŚ/277). Postcranial section without caudal fin show three preserved abdominal and 17 caudal vertebrae (16th vertebra is shortened). Rib attached at parapophysis of last abdominal vertebra. Preserved dorsal fin shows one spine, 11 rays, four finlets; anal fin with one spine, 11 rays, four finlets. Body covered by small cycloid scales.
Remarks The specimen is classified within Scombridae, but a more precise classification is still under study.
Family Trichiuridae Rafinesque, 1810
Genus Anenchelum Blainville, 1818
Material examined 62 specimens—UR/KBŚ/45, 52, 100, 106, 107, 194–196, 198, 225–227, 233, 234, 306, 329, 331, 334, 351, 362, 365, 366, 398, 402, 406, 415, 416, 430, 431, 441–443, 459, 460, 462, 463, 473–475, 504, 508, 515, 521, 552, 573, 609, 621, Pi-F/MP/15, 18, 21/1591/11, Pi-F/MP/1, 14/1592/11, Pi-F/MP/2/1593/11, Pi-F/MP/69, 72, 74, 75, 81, 96, 105, 108, 109, /1598/11 (some of them with counterpart).
Description Severely fragmented material (especially in bigger specimens) does not allow a complete description of this strongly elongated fish. Head tapered anteriorly, with terminal mouth; lower jaw joint at level of anterior portion of orbit. The surface of anterior-most part of dentary bears strong dermal sculpturing. Premaxilla and dentary bear teeth (there are two types of teeth recognizable in the premaxilla; character of teeth in the dentary is not clear). Seven branchiostegal rays. Vertebral column not complete in any specimen; 39 vertebrae present in abdominal part. Dorsal fin starts just behind head, number of spines and rays not known. Interstitial pterygiophores visible in some specimens. Pectoral fins elongate. Pelvic fins reduced to flattened spines. Other details not visible.
Remarks Along with bigger specimens, some presumed to be larvae and juveniles specimens were discovered. Trichiurids are commonly found in the Paratethys region, and are classified within several species (for details see Bannikov 2010), with the most common species beeing A. glarisianum in the Central Paratethys (for more information see new morphological study by Gregorová 2010).
Family Propercarinidae Bannikov, 1995
Genus Propercarina Paucă, 1929
Propercarina problematica Přikryl, Bannikov, Grădianu, Kania & Krzemiński, 2014
Synonymy Refer to Přikryl et al. (2014).
Material examined Single specimen—Pi-F/MP/170/1626/14 (part and counterpart).
Remarks The species was described in detail by Přikryl et al. (2014). The specimen was collected in the “R” section of the outcrop.
Order Pleuronectiformes Bleeker, 1859
Genus and species indeterminate
Material examined Single specimen—Pi-F/MP/15/1572/10 (part and counterpart).
Remarks This poorly preserved specimen is classified as a flatfish due to its overall appearance. The specimen is currently under closer study.
The above descriptions of about seven hundred specimens cover a good representative sample of the fish fauna of the Hermanowa locality (an additional more than one hundred catalogued specimens have not yet been classified more precisely). Although the locality also provided abundant lepidological (i.e., scales) and ichnological (coprolites and rare bioturbation) material, along with scarce remains of swimming crabs (Portunus sp.) and sea turtles (?Glarichelys sp.), these specimens were not taken into account herein.
Although elasmobranchs are not present in large numbers (fewer than 0.5 %), the material shows there was a greater diversity of sharks in the Polish Carpathians than was previously assumed, with the newly recognized presence of Physogaleus latus. This species was described from several localities of the Paratethys realm, but was initially recognized in Oligocene sediments of the region (the species was not mentioned by Kotlarzyk et al. 2006, nor by Bieńkowska-Wasiluk and Radwański 2009). The remainder (i.e., overwhelming part) of the assemblage is represented by teleosts. Also notable is the presence of two clearly different forms of caproids in the single locality.
Typical meso- to bathy-pelagic fishes (such as gonostomatids and/or myctophids) are missing, and the dominant part of the assemblage is composed of the neritic argentinid “Glossanodon” musceli (about 45 %) and clupeids (about 20 %). Other taxa are significantly underrepresented; more than 5 % representation was noted only in the trichiurid Anenchelum (about 9 %), the morid Eophycis jamnensis (about 6.5 %), and the perciforms Trachinus minutus (about 6.5 %), and Oliganodon budensis (about 6.5 %). Acanthopterygians (as a whole) represent slightly more than 25 %, but are very diverse, with more than 16 recognized taxa. Other groups are present in significantly smaller numbers.
Therefore, the locality is similar (in primary qualitative features) to Jamna Dolna D-G, Leszczawa (Jerzmańska 1968: table 8), Rogi (Kotlarczyk et al. 2006), and Rudawka Rymanowska (Bieńkowska-Wasiluk 2010), and in addition to the Polish Carpathians, a similar assemblage was described from the Bystré locality in the Central Paleogen of Slovakia (Gregorová et al. 2012). Surprisingly, the presence of some taxa, such as centriscids and Priacanthus longispinus suggests also an affinity to other IPM zones (such as IPM 1, 4, 4A, 6; for details see Kotlarczyk et al. 2006); nevertheless, these deviations are hard to interpret at the present time (many authors consider IPM zonation to be tentative).
An interesting question is the estimation of the original palaeobathymetry of the locality. As was mentioned above, the greatest part of the assemblage is composed by neritic fishes. Furthermore, practically all of the specimens (with the exception of specimens of Anenchelum) are individuals of small size (max-SL barely 10 cm), which are supposedly easily influenced by water currents. Thus, it is difficult to estimate the original bathyal conditions, but the absence of gonostomatids and myctophids (commonly found in many non-IPM2 localities of the Polish Carpathians; see Kotlarczyk et al. 2006) does not suggest the area was originally a typical deep-water environment.
Furthermore, light-colored fine-grain sediments have exceptional preservation allowing the recognition of early developmental stages of some taxa. Non-adult specimens of different taxa (together with Trachinus and Hipposyngnathus specimens) are relatively common throughout the whole section, but are most common in the lower part of the “H5” layer (that is probably equivalent of the layer “E” sensu Kotlarczyk et al. 2006, p 39). This ontogenetically immature assemblage is outstandingly preserved due to specific taphonomic conditions (although difficult to specify more precisely at the moment), probably related to a hypo- to anoxic regime close to the bottom. The non-adult specimens provide data on the ontogenetic variability of taxa under consideration, and evaluation of the true importance of selected features (such as in Eophycis jamnensis and Trachinus minutus; see Přikryl 2015a, b, respectively) and the locality such supplies new information regarding the non-adult fish-fauna of the Paratethys (previously studied properly only by very few authors, such as e.g., Świdnicki 1988; or Micklich et al. 2009).
The other very productive part of the section is the so called “R layers”, with trachinids, Palaeogadus, “Glossanodon”, ammodytids and Propercarina. This section is also atypical for the profile in having significantly more diatomaceous sediment. It is difficult to definitively classify these layers as related to mass mortality (although fossils in this section of the outcrop are more numerous than in other parts), but probably they may be related, as are other parts of the profile, to an insufficiently ventilated (oxygenated) environment, as was generally mentioned by Báldi (1980).
The collection of fossil fish from the Hermanowa locality (Rupelian) provides following data:
The assemblage is composed of two elasmobranch taxa (Keasius parvus, Physogaleus latus) and 22 taxa of teleosts (Sardinella cf. S. sardinites, Clupeidae gen. et sp. indet., “Glossanodon” musceli, Holosteus sp., Eophycis jamnensis, Palaeogadus sp., Hemiramphidae gen. et sp. indet., Syngnathidae gen. et sp. indet., Hipposyngnathus neriticus, Centriscidae gen. et sp. indet., Priacanthus longispinus, Repropca sabbai, Carangidae gen. et sp. indet., Oliganodon budensis, Ammodytidae gen. et sp. indet., Trachinus minutus, Capros rhenanus, Capros cf. C. caprosoides, Scombridae gen. et sp. indet., Anenchelum sp., Propercarina problematica, and Pleuronectiformes gen. et sp. indet.).
Physogaleus latus is recognized for the first time in the Polish Carpathians.
Typical meso- and bathy-pelagic fish taxa are missing and the dominant part of the assemblage is composed of the neritic fishes with very diverse acanthopterygians.
It is difficult to estimate the original bathyal conditions of the locality.
Light-colored fine-grain sediments have exceptional preservation allowing the recognition of early developmental stages of some taxa, most common in the lower part of the “H5” layer.
Afsari, S., Yazdi, M., Bahrami, A., & Carnevale, G. (2014). A new deep-sea hatchetfish (Teleostei: Stomiiformes: Sternoptychidae) from the Eocene of Ilam, Zagros Basin, Iran. Bollettino della Societ à Paleontologica Italiana, 53, 27–37.
Arambourg, C. (1967). Résultats scientifiques de la mission C. Arambourg en Syrie et en Iran (1938–1939). II – Les Poissons oligocène de l’Iran. Notes et Mémoires sur le Moyen-Orient, 8, 11–210.
Baciu, D.-S., Bannikov, A. F., & Tyler, J. C. (2005). Revision of the fossil fishes of the family Caproidae (Acanthomorpha). Studi e Ricerche sui Giacimenti Terziari di Bolca, 11, 7–74.
Báldi, T. (1980). The early history of the Paratethys. Földtani Közlöni, 110, 456–472.
Bannikov, A. F. (1991). A new family of Oligocene perciform fishes. Paleontological Journal, 25, 88–94.
Bannikov, A. F. (2010). Fossil vertebrates of Russia and adjacent countries. Fossil Acanthopterygians Fishes (Teleostei, Acanthopterygii) (p. 243). Moscow: GEOS.
Bieńkowska-Wasiluk, M. (2010). Taphonomy of oligocene teleost fishes from the outer carpathians of Poland. Acta Geologica Polonica, 60, 479–533.
Bieńkowska-Wasiluk, M., & Bonde, N. (2015). A new oligocene relative of the caproidae (Teleostei: Acanthopterygii) from the outer carpathians, Poland. Bulletin of Geosciences, 90, 461–478.
Bieńkowska-Wasiluk, M., & Radwański, A. (2009). A new occurrence of sharks in the Menilite Formation (Lower Oligocene) from the Outer (Flysch) Carpathians of Poland. Acta Geologica Polonica, 59, 235–243.
Birdsong, R. S., Murdy, E. O., & Pezold, F. L. (1980). A study of the vertebral column and median fin osteology in gobioid fishes with comments on gobioid relationships. Bulletin of Marine Science, 42, 174–214.
Bor, T. J. (1980). Elasmobranchii from the Atuatuca Formation (Oligocene) in Belgium. Mededelingen van de Werkgroep voor Tertiaire en Kwartaire Geologie, 17, 3–16.
Cappetta, H. (2012). Handbook of Paleoichthyology. Vol 3B. Chondrichthyes (Mesozoic and Cenozoic Elasmobranchii: Teeth) (p. 512). Stuttgart: Gustav Fisher.
Carnevale, G., Bannikov, A. F., Landini, W., & Sorbini, C. (2006). Volhynian (early Sarmatian sensu lato) fishes from Tsurevsky, North Caucasus, Russia. Journal of Paleontology, 80, 684–699.
Carnevale, G., Bannikov, A. F., Marramà, G., Tyler, J. C., & Zorzin, R. (2014). The Pesciara-Monte Postale Fossil-Lagerstätte: 2. Fishes and other vertebrates. Rendiconti della Società Paleontologica Italiana, 4, 37–63.
Ciobanu, R. (2002). Selacienii paleogeni din Romania (p. 216). Sibiu: Editura Universităţii Lucian Blaga.
Constantin, P. (2001). Holosteus fieniensis n. sp., a new fossil fish (Teleostei: Paralepididae) in the Rupelian formation from Fieni (Eastern Carpathians, Romania). Acta Paleontologica Romaniae, 3, 77–86.
Cosmovici, L. C. (1887). Les couches a poissons des Monts Petricica et Cozla, district de Neamtz, Ville de Peatra. Buletin de Societate Medici si Naturalisti, Iasi, 1, 96–105.
Daniltshenko, P. G. (1960). Kostistiye ryby maikopskich othlozeniy Kavkaza. Trudy Paleontologicheskogo Instituta AN SSSR, 78, 1–208.
Daniltshenko, P. G. (1980). Otryad Clupeiformes. In L. I. Novitskaya (Ed.), Iskopayemyye kostistyye ryby SSSR (pp. 7–26). Trudy Paleontologicheskogo Instituta Akademii Nauk SSSR, 178.
Fritzsche, R. A. (1980). Revision of the eastern Pacific Syngnathidae (Pisces: Syngnathiformes), including both recent and fossil forms. Proceedings of the California Academy of Sciences, 42, 181–227.
Grande, L. (1985). Recent and fossil clupeomorph fishes with materials for revision of the subgroups of clupeoids. Bulletin of the American Museum of Natural History, 181, 231–372.
Gregorová, R. (2010). Osteological and morphological analysis of the scabbardfish Anenchelum glarisianum BLAINVILLE, 1818 (Trichiuridae) from the Menilitic Formation of the Moravian part of West Carpathians (Oligocene, Rupelian). Acta Musei Moraviae, 95, 141–149.
Gregorová, R. (2011). Fossil fish fauna (Teleostei, Selachii) from the Dynów marlstone (Rupelian, NP 23) of the Menilitic Formation at the locality of Litenčice (Czech Republic). Acta Musei Moraviae, Scientiae Geologicae, 96, 3–33.
Gregorová, R., Soták, J., & Krempaská, Z. (2012). Nové poznatky o rybí fauně centrálního karpatského paleogénu z locality Bystré. Spiš, vlastivědný sborník, 6, 121–122.
Hovestadt, D. C., & Hovestadt-Euler, M. (2012). A partial skeleton of Cetorhinus parvus Leriche, 1910 (Chondrichthyes, Cetorhinidae) from the Oligocene of Germany. Paläontologische Zeitschrift, 86, 71–83.
Jerzmańska, A. (1960). Ichtiofauna lupków jasielskich z Sobniowa. Acta Palaeontologica Polonica, 5, 367–419.
Jerzmańska, A. (1967). Argentinidés (Poissons) fossiles de la série ménilitique des Karpates. Acta Palaeontologica Polonica, 12, 195–211.
Jerzmańska, A. (1968). Ichtyofaune des couches à ménilite (flysch des Karpathes). Acta Palaeontologica Polonica, 13, 379–487.
Jerzmańska, A. (1974). Kotlarczykia bathybia gen. n., sp. n. (Teleostei) from the Oligocene of the Carpathians. Acta Palaeontologica Polonica, 19, 281–289.
Jerzmańska, A. (1979). Oligocene alepocephaloid fishes from the polish Carpathians. Acta Palaeontologica Polonica, 24, 65–76.
Jerzmańska, A., & Kotlarczyk, J. (1975). Kopalny zespól quasi-sargassowy z warstw menilitowych jednotki sokolskiej Karpat polskich. Kwartalnik Geologiczny, 19, 875–886.
Jerzmańska, A., & Kotlarczyk, J. (1976). The beginnings of the Sargasso assemblage in the Tethys? Palaeogeography, Palaeoclimatology, Palaeoecology, 20, 297–306.
Jerzmańska, A., & Świdnicka, E. (2003). Echeneis carpathica Szajnocha, 1926 w profilu warstw menilitowych polskich Karpat. Przegląd Geologiczny, 51, 254.
Kotlarczyk, J., & Jerzmańska, A. (1976). Biostratigraphy of menilite beds of Skole Unit from the Polish flysch Carpathians. Bulletin de L’Academie Polonaise des Sciences. Série des Sciences de la Terre, 24, 55–62.
Kotlarczyk, J., Jezmańska, A., Świdnicka, E., & Wiszniowska, T. (2006). A framework of ichthyofaunal ecostratigraphy of the Oligocene-Early Miocene strata of the Polish Outer Carpathian basin. Annales Societatis Geologorum Poloniae, 76, 1–111.
Kozdęba, B. (2008). Ryby oligoceńskie ze stanowiska w Hermanowej koło Rzeszowa ze szczególnym uwzględnieniem gatunku Glossanodon musceli przedstawiciela rodziny Argentinidae. Mgr. thesis, Uniwersytet Rzeszowski, Rzeszow, Poland, p. 59.
Leriche, M. (1910). Les poissons Oligocènes de la Belgique. Mémoires du Musée royal d’histoire naturelle de Belgique, 5, 229–363.
Micklich, N. (1998). New information on the fishfauna of the Frauenweiler fossil site. Italian Journal of Zoology, 65, 169–184.
Micklich, N., & Parin, N. (1996). The fishfauna of Frauenweiler (Middle Oligocene, Rupelian; Germany): first results of a review. Publicaciones Especiales de Instituto Español de Oceanografía, 21, 129–148.
Micklich, N. R., Tyler, J. C., Johnson, G. D., Świdnicka, E., & Bannikov, A. F. (2009). First fossil records of the tholichthys larval stage of butterfly fishes (Perciformes, Chaetodontidae), from the Oligocene of Europe. Paläontologische Zeitschrift, 83, 479–497.
Parin, N., & Micklich, N. (1996). Fossil gasterosteiformes from the lower Oligocene of Frauenweiler (Baden-Württemberg, Germany) I. New information on the morphology and systematics of the genus Aeoliscus Jordan & Starks 1902. Paläontologische Zeitschrift, 70, 521–545.
Paucă, M. (1929). Vorläufige Mitteilung über eine fossile Fischfauna aus den Oligozänschiefern von Suslanesti. Bulletin de la Section Scientifique Académie Roumaine, 12, 112–120.
Paucă, M. (1934). Die fossile Fauna und Flora aus dem Oligozän von Suslanesti-Muscel in Rumänia. Anuarul Instiutului Geologic al Romaniei, 16, 575–668.
Pharisat, A. (1991). La paleoichthyofaune du Rupelien marin de Froidefontaine. Annales de la Société Université de Franche-Comté Besancon, Géologie, 4, 13–97.
Pharisat, A. (1998). Marine fish biodiversity in the Oligocene of Froidefontaine (Belfort Territory, France). Italian Journal of Zoology, 65, 189–191.
Pharisat, A., & Micklich, N. (1998). Oligocene fishes in the western paratethys of the Rhine Valley Rift System. Italian Journal of Zoology, 65, 163–168.
Přikryl, T. (2009). A juvenile Trachinus minutus (Pisces, Perciformes, Trachinidae) from the Middle Oligocene of Litenčice (Moravia, Czech Republic). Acta Musei Nationalis Pragae, Series B, Historia Naturalis, 65, 3–8.
Přikryl, T. (2013). An annotated list of the Oligocene fish fauna from the Osíčko locality (Menilitic Fm.; Moravia, the Czech Republic). Acta Musei Nationalis Pragae, Series B, Historia Naturalis, 69, 195–203.
Přikryl, T. (2015a). Skeletal anatomy of the early morid fish Eophycis (Gadiformes, Moridae) from an Oligocene deposit in Poland. Comptes Rendus Palevol, 14, 625–635.
Přikryl, T. (2015b). Notes on development of the Oligocene trachinid Trachinus minutus (JONET, 1958). Palaeontographica Abt. A. (accepted)
Přikryl, T., Bannikov, A. F., Grădianu, I., Kania, I., & Krzemiński, W. (2014). Revision of the family Propercarinidae (Perciformes, Stromateoidei) with description of a new species from the Oligocene of the Carpathians. Comptes Rendus Palevol, 13, 691–700.
Přikryl, T., Krzemiński, W., & Kania, I. (2011). New information about the anatomy of a peculiar fish of the genus Hipposyngnathus Daniltshenko, 1960. Comptes Rendus Palevol, 10, 559–566.
Prokofiev, A. M. (2005a). Holosteinae, a New Subfamily of Paralepidids (Alepisauroidei: Paralepididae). Journal of Ichthyology, 45, 275–283.
Prokofiev, A. M. (2005b). Revision of Protacanthopterygii (Osteichthyes: Euteleostei) from Cenozoic marine deposits of the Caucasus and Turkmenistan: I. The orders Argentiniformes and Salmoniformes s.str. (Sensu Johnson, Patterson, 1996) in the Oligocene–Miocene of the Caucasus. Journal of Ichthyology, 45, 5–20.
Prokofiev, A. M. (2013). Two new species of families Priacanthidae and Reproprcidae (Perciformes) from the upper part of Lower Oligocene of the Northern Caucasus. Journal of Ichthyology, 53, 245–251.
Reinecke, T., Von der Hocht, F., & Dufraing, L. (2015). Fossil basking shark of the genus Keasius (Lamniformes, Cetorhindiae) from the boreal North Sea Basin and Upper Rhine Graben: evolution of dental characteristics from the Oligocene to late Middle Miocene and description of two new species. Palaeontos, 28, 39–98.
Roberts, C. D. (1993). Comparative morphology of spined scales and their phylogenetic significance in the Teleostei. Bulletin of Marine Science, 52, 60–113.
Świdnicki, J. (1988). Juveniles of some Oligocene Antigonia (Caproidae, Teleostei), from the Polish Carpathians. Acta Palaeontologica Polonica, 33, 249–259.
Szymczyk, W. (1978). Clupeid scales from the Menilite Beds (Palaeogene) of the Carpathians. Acta Palaeontologica Polonica, 23, 387–407.
von Rath, G. (1859). Beiträge zur Kenntniss der fossilen Fische des Plattenberges im Canton Glarus. Zeitschrift der Deutschen Geologischen Gesellschaft, 11, 108–132.
Weiler, W. (1938). Neue Untersuchungen an Mitteloligozänen Fischen Ungarns. Geologica Hungarica, Series Palaeontologica, 15, 1–31.
Welton, B. J. (2013). A new archaic basking shark (Lamniformes: Cetorhinidae) from the Late Eocene of Western Oregon, U.S.A., and description of the dentition, gill rakers and vertebrae of the Recent basking shark Cetorhinus maximus (Gunnerus). New Mexico Museum of Natural History and Science, Bulletin, 58, 1–48.
Wettstein, A. (1886). Über die Fischfauna des tertiären Glarnerschiefers. Abhandlungen der Schweizerischen Paläontologischen Gesellschaft, 13, 1–103.
The authors are grateful to A.F. Bannikov (Moscow), B. Ekrt (Prague), R. Gregorová (Brno), N. Micklich (Darmstadt), and E. Świdnicka (Wroclaw) for access to the collections under their care and/or consultations. Petr Daneš (Prague) and Sabina Schuster (Paris) are acknowledged for linguistic support. Both anonymous reviewers are acknowledged for their notes that improved quality of earlier version of the manuscript and Alison Murray (Edmonton) is acknowledged for her help with final langue corrections. Daniel Marty (Basel) is acknowledged for his help during editorial process. The research was financially supported by Czech science foundation (GAČR) Project No. GP13-19250P and by institutional project RVO67985831 (Institute of Geology of the CAS, v.v.i.).
Editorial handling: D. Marty.
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Přikryl, T., Kania, I. & Krzemiński, W. Synopsis of fossil fish fauna from the Hermanowa locality (Rupelian; Central Paratethys; Poland): current state of knowledge. Swiss J Geosci 109, 429–443 (2016). https://doi.org/10.1007/s00015-016-0216-5