www.geologicacarpathica.sk
GEOLOGICA CARPATHICA, AUGUST 2009, 60, 4, 283—294 doi: 10.2478/v10096-009-0020-5
Latest Maastrichtian foraminiferal assemblages from the
Husów region (Skole Nappe, Outer Carpathians, Poland)
M. ADAM GASIŃSKI and ALFRED UCHMAN
Institute of Geological Sciences, Jagiellonian University, Oleandry Str. 2a, PL-30-063 Kraków, Poland;
adam.gasinski@uj.edu.pl; alfred.uchman@uj.edu.pl
(Manuscript received August 25, 2008; accepted in revised form December 18, 2008)
Abstract: The Ropianka Formation (also known as the Inoceramian Beds) in the marginal part of the Skole Nappe
(Husów region, the Gaj section) contains abundant, diverse and well preserved assemblages of Maastrichtian planktonic
and benthic foraminiferids, assigned to the middle-upper part of the Gansserina gansseri Zone and to the Abathomphalus
mayaroensis Zone. The composition of the assemblages indicates fluctuations of organic matter flux to the marginal
part of the Skole Basin floor in the studied interval. The studied taxa are typical of the “transitional zone” between the
Tethyan and the Boreal domains. The disappearance of planktonic foraminifers in the uppermost part of the section and
appearance of some agglutinated taxa (Rzehakina fissistomata; abundant Conglophragmium irregularis and Glomospira
charoides) points to a Paleocene age.
Key words: Maastrichtian, flysch, transitional zone, paleoecology, biostratigraphy, foraminiferids.
Introduction
Terminal Maastrichtian foraminiferal assemblages in the Flysch
Carpathians are represented by mostly poorly diagnostic
benthic agglutinated taxa. The foraminiferal zones based on
them (Geroch & Nowak 1984; Olszewska 1997) are broad in
duration. As a consequence a precise stratigraphy of this inter-
val is very difficult, and determination of the K/T boundary is
imprecise. Exceptionally, some taxa of the youngest Creta-
ceous planktonic foraminiferal Abathomphalus mayaroensis
Zone have been found in a few sections of the Subsilesian
Unit (Gasiński et al. 1999, 2001) and the Skole Nappe (see
chapter
Micropaleontological analysis
).
Very rich assemblages of planktonic and benthic foramini-
fers of youngest Maastrichtian age occur in flysch sedi-
ments of the marginal thrust sheet in the Skole Nappe, SE
of Rzeszów in the Husów region (Fig. 1). Their description
and interpretation are the main aim of the paper.
The biostratigraphy of the Cretaceous in the study area is
so far poorly recognized, without modern micropaleontolog-
ical research. Such abundant, very diverse and well pre-
served Maastrichtian planktonic foraminiferal assemblages
are very rarely found in the Polish Flysch Carpathians
(Gasiński et al. 1999, 2001, 2003). Commonly, only some
index taxa are listed but not illustrated. For the first time in
the Skole Unit, the planktonic foraminiferal assemblage al-
low the recognition of recently proposed latest Cretaceous
biozones. Moreover, the microfauna of the Skole Unit con-
tributes to our understanding of migration “gates” between
the Boreal and Tethyan biogeoprovinces (Gasiński 1997,
1998; Marcinowski & Gasiński 2002). The marginal part of
the Skole Unit of the Polish Carpathians was located near the
Boreal-Transitional domain (Kollmann & Zapfe 1992) in
proximity to the so-called Lviv Gate (Marcinowski &
Gasiński 2002). Therefore, micropaleontological data from
this area are very important for reconstructions of the Late
Cretaceous plankton paleobiogeography.
Geological setting
The Skole Nappe SE of Rzeszów has been studied since the
19
th
century. Tietze (1883) distinguished the Ropianka Beds
in the vicinity of Albigowa and ascribed all the flysch deposits
SE of Rzeszów to the “older Tertiary”, and Hilber (1885) as-
signed them to the Neocomian. Friedberg (1900) also distin-
guished the Ropianka Beds at Albigowa and Husów.
Wdowiarz (1936, 1949) characterized the lithostratigraphy
and tectonics of the Cretaceous and younger deposits of this
area. He recognized the Inoceramian Beds (formerly known as
the Ropianka Beds), subdivided them into the lower, middle
and upper levels, estimated their thickness at 500 m, and dated
them to the Senonian—Paleocene by analogy to other areas.
They are overlain by the Eocene Variegated Shale. For a com-
prehensive history of research on the Ropianka Beds (latter
Ropianka Formation or Inoceramian Beds) in the Skole Nappe
see Kotlarczyk (1978). Bromowicz (1974) described the li-
thology and distinguished four lithological complexes in the
Inoceramian Beds in the area SE of Rzeszów, the total thick-
ness of which was estimated at about 400 m. Bromowicz de-
termined that their sediments were transported from the NW.
West of the study area, Malata (2001) distinguished the Fu-
coid Marl Member, Leszczyny Sandstone Member (Maastrich-
tian) and the Makówka Slump Debris (Late Maastrichtian)
within the Ropianka Formation which was renamed as the
Rybotycze Formation.
At first in the 19
th
century, the studied deposits of the Skole
Nappe were named the Ropianka Beds, which were originally
distinguished in the Magura Nappe (Paul 1869). Later, these
deposits were called the Inoceramian Beds (Uhlig 1888;
284
GASIŃSKI and UCHMAN
Wdowiarz 1949). Kotlarczyk (1978) applied the oldest name
to the Inoceramian Beds of the Skole Nappe and established
the Ropianka Formation with its neostratotype in the Przemyśl
area, which he (see also Kotlarczyk 1979, 1985) subdivided
into the Cisowa Member (Turonian—Lower Campanian),
Wiar Member (Lower Campanian—Lower Maastrichtian),
Leszczyny Member (Lower Maastrichtian—Lower Paleo-
cene) and Wola Korzeniecka Member (Paleocene) (Fig. 2).
This lithostratigraphic scheme was a matter of controversies
(Haczewski 1986; Ślączka & Miziołek 1995; Malata 1996,
2001) but new propositions, if present (Malata 1996, 2001),
are also problematic. These problems require clarification
that is beyond the scope of this study.
The oldest biostratigraphic data in the studied area come
from the 19
th
century. Hilber in Uhlig (1883) and Grzybowski
(1903) found inoceramid bivalve fragments at Husów (their
Hussow) pointing to the Cretaceous. Friedberg (1901, 1903)
determined the foraminifers Dendrophrya excelsa Grzybowski,
D. robusta Grzybowski and D. robusta var. maxima from in-
tercalations of sandstones and shales at Albigowa, probably
from the Inoceramian Beds. Friedberg (1908) determined
Inoceramus salisburgensis Fugger & Kastner from Husów.
The studied section occurs along the Gajowy stream, in
the Gaj forest between the territories of the villages of
Fig. 1. Location map. Tectonic unit designation, Carpathian margin
and range of the Variegated Shale after Wdowiarz (1949). Location
of samples (Gaj 1, etc.) indicated.
Fig. 2. Stratigraphic scheme of the Skole Nappe. Based on Kot-
larczyk (1988), Rajchel (1990), Rajchel & Uchman (1998), Ślączka
& Kaminski (1998), with further corrections based on further data
by Gedl (1999) and Kotlarczyk et al. (2007). The investigated in-
terval indicated by “!”. The time scale is after Gradstein et al. (2004).
TRShMb – Trójca Red Shale Member, VSh – Variegated Shale,
ChSMb – Chmielnik Striped Sandstone Member.
285
LATEST MAASTRICHTIAN FORAMINIFERAL ASSEMBLAGES (HUSÓW REGION, POLAND)
Husów, Handzlówka and Albigowa (Fig. 1). The outcrops are
small and isolated (sections A—D in Fig. 3), but the conse-
quent strikes and dips of beds suggest a limb of a regular anti-
cline with its axis dipping to the west. The anticline is a part of
the Marginal Thrust Sheet, the structure of which is more
complex to the NW (Wdowiarz 1949). The Marginal Thrust
Sheet is overthrust to the NE onto the Miocene of the Stebnik
Unit (or Zgłobice Unit according to Kotlarczyk 1988) or on
the autochthonous Miocene of the Carpathian Foredeep. To
the SE, the Ropianka Formation of the Marginal Thrust Sheet
is bound by a belt of Eocene Variegated Shale, which also be-
longs to the Marginal Thrust Sheet. Further to the South, the
Husów Thrust Sheet is present, which is overthrust onto the
Marginal Thrust Sheet (Wdowiarz 1949).
The studied outcrops are composed of turbiditic deposits
with a great contribution of marls and marly shales interca-
lated with fine- to medium-grained calcareous sandstones
(Fig. 3). The lower part of the studied sequence (sections A
and B) contains more sandstones, with beds up to 30 cm
thick. The upper part (sections C, D) contains less sand-
stones, with thinner beds. These deposits contain the trace
fossils Ophiomorpha rudis (especially in thicker beds),
Chondrites targionii, and rarely Nereites irregularis and
Phycosiphon incertum. Stratigraphically, the studied depos-
its are an equivalent of the Leszczyny Member and possibly
of the uppermost part of the Wiar Member of the Ropianka
Formation sensu Kotlarczyk (1978, 1988) (Fig. 2). The li-
thology of the Leszczyny Member is very variable and in-
cludes marl-rich olistostromes. It is not clear whether the
Wiar Member or the Leszczyny Member can be distin-
guished in the study area, however a general fining-up sec-
tion is one of the typical features of the Leszczyny Member
(Kotlarczyk 1978) and these members are recognized west of
the study area (J. Kotlarczyk, personal communication,
2008). The divisions recognized by Malata (2001) in the
same tectonic units, namely the Leszczyny Sandstone Mem-
ber (thick-bedded sandstones at least 100 m thick) and the
Makówka Slump Debris Member, which can be expected to
occur in the studied section because of their stratigraphic po-
sition, are not recognized here.
Micropaleontological analysis
Biostratigraphy
Twenty five samples from the section studied area have
been analysed (see: Figs. 3, 4). Some of these contain well
Fig. 3. Lithological column with location of the samples.
286
GASIŃSKI and UCHMAN
Fig. 4. Species occurrence in the studied samples. For biozones see Fig. 5.
287
LATEST MAASTRICHTIAN FORAMINIFERAL ASSEMBLAGES (HUSÓW REGION, POLAND)
and very well preserved planktonic and benthic foraminifer-
ids (Figs. 4, 5). The stratigraphic ranges of the index taxa
point to a Maastrichtian age. The middle to upper part of the
Gansserina gansseri to Abathomphalus mayaroensis stan-
dard zones were distinguished according to the zonation
published by Caron (1985), Robaszynski & Caron (1995;
Fig. 5). These zones have been recognized on the basis of in-
dex planktonic foraminiferids as well as characteristic fora-
miniferal assemblages. The Abtahomphalus mayaroensis
Zone is a Taxon Range Zone. It was recognized between sam-
ple Gaj 4.1, where the first appearance (FO) of A. mayaroensis
(Bolli) is noted, and sample Gaj 5.7, where its last occur-
rence (LO) is observed (Fig. 5). Gansserina gansseri (Bol-
li) is not present in the analysed material, probably due to
its more Tethyan paleobiogeographic preferences. Neverthe-
less, the stratigraphic ranges of other planktonic species, such
as: Pseudotextularia elegans (Rzehak), Globigerinelloides
prairiehillensis Pessagno, Hedbergella holmdelensis Olsson,
Globotruncana aegyptiaca Nakkady, G. bulloides Vogler and
G. stuartiformis (Dalbiez), and the absence of Abathomphalus
mayaroensis (Bolli) in sample Gaj 1 to Gaj 4 (below its FO)
points to the underlying Gansserina gansseri Zone (Fig. 4).
Abathomphalus mayaroensis is rarely noted from the tur-
biditic sequences of the Outer Carpathians (e.g. Liszkowa &
Morgiel 1981; Gasiński et al. 2001). However, this species is
never abundant and occurs in assemblages together with oth-
er planktonic species, such as Heterohelix navarroensis
Ehrenberg, H. striata (Ehrenberg), Pseudotextularia elegans
(Rzehak), Racemiguembelina fructicosa (Egger), Globige-
rinelloides prairiehillensis Pessagno, Hedbergella holmde-
lensis Olsson, H. monmouthensis (Olsson), Globotruncana
aegyptiaca Nakkady, G. arca (Cushman), G. bulloides Vo-
gler, Globotruncanita stuarti (de Lapparent), G. stuartiformis
(Dalbiez), Globotruncanella havanensis (Voorvijk), G. peta-
loidea (Gandolfi), or Contusotruncana contusa (Cushman)
(Fig. 4). All the diagnostic species as well as some taxa
which are typical of the studied foraminiferal assemblages
are illustrated in Figures 7—9. Their stratigraphic ranges are
reported after Robaszynski et al. (1984), Caron (1985),
Robaszynski & Caron (1995), Premoli-Silva & Rettori
(2002) and Premoli-Silva & Verga (2004).
Foraminiferal assemblages from sample Gaj 5.7A to sam-
ple Gaj 6A (Fig. 4) are composed mainly of agglutinated
taxa, with a small admixture of calcareous benthic forms.
They do not contain any planktonic taxa. Therefore, it is
impossible to determine their precise biostratigraphical posi-
tion to a particular biozone, however some suggestions
based on composition of the agglutinated foraminiferal as-
semblages can be made. Samples Gaj 5.7A, 5.8 and 5.9 con-
tain among others the agglutinated index species Rzehakina
fissistomata (Grzybowski), which ranges from the ?Maas-
trichtian to the Paleocene (Kaminski & Gradstein 2005).
Liszkowa & Morgiel (1981) have dated an agglutinated for-
aminiferal assemblage with Rzehakina fissistomata from the
Fig. 5. Biostratigraphical ranges of the studied planktonic index taxa. Ranges of species
and biozones plotted (combined) after Robaszynski et al. (1984), Caron (1985), Robaszyns-
ki & Caron (1995), Premoli-Silva & Rettori (2002) and Premoli-Silva & Verga (2004). The
grey area indicates biozones recognized in the studied material.
Krasice section of the Skole Unit as Pa-
leocene. Sample Gaj 6 does not contain
index taxa, but the increased abundance
of Conglophragmium irregularis (White)
and Glomospira charoides (Parker &
Jones) points to the Paleogene. The
same concerns sample Gaj 6A, which
additionally contains Karrerulina con-
versa (Grzybowski) and K. horrida
(Mjatliuk). The higher abundance of
shales in this part of the section
(Figs. 3, 4) suggests a change in depo-
sitional conditions.
Abathomphalus mayaroensis (Bolli)
in the Skole Nappe
Abathomphalus mayaroensis (Bolli)
(formerly Globotruncana mayaroensis
Bolli) has been recognized by Bukowy
& Geroch (1957) in the K. Wójcik col-
lection of foraminiferids from the exot-
ic conglomerates at Kruhel Wielki near
Przemyśl. Morgiel (1959) and Szyma-
kowska (1961) mentioned the occur-
rence of this species in the Babica Clay.
The Babica Clay is composed mostly of
debris flow deposits and is dated to the
Paleocene
(Bukowy
1956,
1957;
Geroch & Kotlarczyk 1963). It seems
that A. mayaroensis in this unit is rede-
posited from Maastrichtian sediments.
288
GASIŃSKI and UCHMAN
Other findings of Abathomphalus mayaroensis come from
the Ropianka Formation of the Skole Nappe but these obser-
vations are rarely supplemented by detailed localization.
Morgiel & Żgiet (1961) mentioned G. mayaroensis in sam-
ples from the borehole at Dydnia (their Inoceramian Beds of
the Subsilesian and Skole Units transitional zone). Glo-
botruncana mayaroensis is listed among the foraminiferal
assemblages of the Ropianka Formation (Inoceramian Beds)
as well as those of the Węgierka Marls (upper part of the
Ropianka Formation) (Gucik 1962, 1987; Gucik & Wójcik
1982; Kotlarczyk 1988). It was also listed by Bieda et al.
(1963) from the Węglówka Marl and the Żegocina Marl of
the Subsilesian Unit. Vialov et al. (1967) and Zhurakovsky
(1971) reported findings of G. mayaroensis in the Ukrainian
part of the Skole Nappe. Morgiel in Wdowiarz et al. (1974)
mentioned it from the Cisowa IG-1 borehole. Morgiel &
Liszkowa (1981) informed about relatively numerous speci-
mens of A. mayaroensis within foraminiferal assemblages of
the Frydek Marl-type sediments of the Subsilesian Unit as
well as from the so-called Baculites Marls (an equivalent of
the Węgierka Marls in the Skole Nappe).
Abathomphalus mayaroensis and associated planktonic and
benthic foraminifers have also been found in the Leszczyny
Member in the Przemyśl area (Kotlarczyk 1988, p. 44). Mor-
giel in Żytko & Zimnal (1997) noted A. mayaroensis from the
foraminiferal association of the Smorż stream section.
Paleoecology
On the basis of washed residues of the collected samples, a
quantitative analysis has been performed (Fig. 6). All speci-
mens, including those with broken tests, were counted. For
the planktonic assemblages, the parameters: planktonic/
benthic ratio and epipelagic/bathypelagic ratio are consid-
ered as indicators of paleobathymetry and offshore distance
(cf. Sliter 1972; Sliter & Baker 1972; Olsson & Nyong 1984;
and others). Within the benthic associations, the agglutinat-
ed/calcareous benthic taxa ratio and the suspension-feeders
(tubular forms such as Rhabdammina or Nothia)/other ag-
glutinated taxa ratio were counted. These results point to the
organic flux (OF) to the basin floor by turbiditic currents and
to its quantitative aspect (cf. Kaminski & Kuhnt 1995;
Gasiński 1998). A distinct negative correlation between an
increase in planktonic and especially epipelagic species and
a reduction in suspension feeders is noted (Fig. 6). Only in
sample Gaj 5.4A does this relation change rapidly; plankton-
ic species became very scarce, whereas suspension feeders
dominate. This could reflect an increase in OF, which may
have been caused by increased productivity or redeposition
of organic matter from the shallower part of the basin due to
a relative sea-level fall. However, the latter possibility is not
marked by any sedimentological change, such as coarsening
of sediments. The relative increase in abundance of the sus-
pension feeder morphological group in relation to relatively
scarce epipelagic taxa is observed in sample Gaj 1. Another
rapid increase in suspension feeder abundance and diminish-
ing abundance of epipelagic planktonic taxa is noted in sam-
ple Gaj 5.5. Such rapid changes among foraminiferal
assemblages of samples Gaj 5.4A and Gaj 5.5 can be inter-
preted as an episode of rapid increase in sea-surface produc-
tivity (especially distinct in sample Gaj 5.4A). The increased
availability of organic matter caused the rapid appearance of
tubular agglutinated taxa (for the feeding strategy of fora-
miniferal suspension feeders see: Jones & Charnock 1985;
Nagy 1992; Kaminski & Kuhnt 1995; Gasiński 1998). It
should be stressed that from sample Gaj 6 (Fig. 6) aggluti-
nated foraminiferids dominate, which indicates a drastic
change in environmental conditions resulting in a change of
composition of foraminiferal assemblages toward decreasing
planktonic taxa. Of course, the activity of turbiditic currents
taking place in the studied part of the Skole Basin strongly
influenced such processes.
Discussion
Biostratigraphy
The chronostratigraphy of the Abathomphalus mayaroen-
sis and Gansserina gansseri Zones has been provided by
Robaszynski & Caron (1995). In their scheme, the Maas-
trichtian comprises the whole of the A. mayaroensis Zone
and the upper part of the G. gansseri Zone. Robaszynski et
al. (1984) and Caron (1985) proposed a different scheme, in
which the underlying G. aegyptiaca and the G. helvetica
Zones are also included into the Maastrichtian. According to
the subsequent schemes by Robaszynski & Caron (1995)
and Premoli-Silva & Rettori (2002), these zones belong into
the upper Campanian. In the current Cretaceous Time Scale,
Gradstein et al. (2004) proposed a Racemiguembelina fructi-
cosa Zone situated between the A. mayaroensis and G. gans-
seri Zones. Racemiguembelina fructicosa (Egger) is present
in the studied material (Fig. 8.3—6), however its occurrence
together with A. mayaroensis (Fig. 4) does not allow us to
separate the Racemiguembelina fructicosa Zone. Racemi-
guembelina fructicosa is rarely noted in foraminiferal assem-
blages of the Tethyan domain (cf. Nederbragt 1991).
It should be mentioned that the Cretaceous/Paleocene
boundary (traditionally named K/T) is placed between the last
occurrence of Abathomphalus mayaroensis (Bolli) and first
abundant appearance of Guembelitria cretacea Cushman,
which constitutes the Partial Range P0 Zone sensu Olsson et
al. (1999) and Gradstein et al. (2004). It is located between the
samples Gaj 5.7 amd Gaj 5.7A of the studied section (Fig. 3),
which are 3 m apart. So far, this is the most precise location of
the K/T boundary in the Polish Carpathians.
Provenience of the studied planktonic assemblage
The Maastrichtian foraminiferal assemblages analysed
from the Husów area (this study) and those from the Węgier-
ka Marls of the Skole Unit (Kotlarczyk 1978; Geroch et al.
1979) display a distinct similarity. The Kropiwnik Fucoid
Marl in the Wiar Member (Kotlarczyk 1978, 1985, 1988)
also contains some similar species of foraminiferids, among
them a few index species such as: Globotruncana arca, Glo-
botruncanita stuarti, Globotruncanella havanensis, and
Contusotruncana contusa.
289
LATEST MAASTRICHTIAN FORAMINIFERAL ASSEMBLAGES (HUSÓW REGION, POLAND)
Fig. 6. Quantitative analysis of the studied foraminiferal assemblages.
290
GASIŃSKI and UCHMAN
Fig. 7. Benthic foraminiferids from the Gaj section. 1 – Hormosina velascoensis (Cushman), sample Gaj 5.8. 2, 3 – Ammodiscus sp., 2 – sam-
ple Gaj 5.3, 3 – sample Gaj 6. 4, 5 – Glomospira charoides (Parker & Jones), 4 – sample Gaj 5.3, 5 – sample Gaj 6. 6 – Conglophrag-
mium irregularis (White), sample Gaj 6. 7 – Karrerulina horrida (Mjatliuk), sample Gaj 6A. 8 – Karrerulina conversa (Grzybowski),
sample Gaj 6A. 9 – Spiroplectammina spectabilis (Grzybowski), sample Gaj 5.4. 10, 11 – Rzehakina epigona (Grzybowski), sample Gaj 5.2.
12, 13 – Rzehakina fissistomata (Grzybowski), sample Gaj 5.9. 14 – Dorothia oxycona, sample Gaj 5.8. 15, 16 – Arenobulimina dorbignyi
(Reuss), sample Gaj 5.6A. 17 – Coryphostoma cf. plaita (Carsey), sample Gaj 5. 18 – Nodosaria sp., sample Gaj 5.3. 19 – Saracenaria cf. tri-
angularis (d’Orbigny), sample Gaj 5.4. 20 – Lenticulina sp., sample Gaj 5.4A.
According to the results of cluster analysis of significant
Campanian—Maastrichtian foraminiferal associations (Gasiński
1998), the considered associations fit within the “transitional
zone” between the Boreal and Tethyan provinces (cf. Gasiński
1997, 1998; Marcinowski & Gasiński 2002). In comparison to
the Maastrichtian foraminiferal assemblages from the Andry-
chów Klippen marls regarded as typical “transitional” biota
between Boreal and Tethyan domains (cf. Gasiński 1998), the
described assemblages do not contain some planktonic genera
(e.g. Rugoglobigerina), that are diagnostic of the Boreal prov-
ince (cf. Scheibnerova 1971; Sliter 1972, 1977; Gasiński
1997). According to Olsson & Wise (1987), Contusotruncana
291
LATEST MAASTRICHTIAN FORAMINIFERAL ASSEMBLAGES (HUSÓW REGION, POLAND)
Fig. 8. Planktonic foraminiferids from the Gaj section. 1, 7 – Heterohelix striata (Ehrenberg), sample Gaj 5. 2 – Pseudotextularia elegans
(Rzehak), sample Gaj 5. 3—6 – Racemiguembelina fructicosa (Egger), sample Gaj 5. 8 – Heterohelix navarroensis Ehrenberg, sample Gaj 5.
9 – Contusotruncana contusa (Cushman), sample Gaj 5. 10 – Hedbergella monmouthensis (Olsson), sample Gaj 5. 11—12 – Hedbergella
holmdelensis Olsson, sample Gaj 5. 13 – Globotruncanella havanensis (Voorwijk), sample Gaj 5. 14 – Globotruncanella petaloidea
(Gandolfi), sample Gaj 5. 15, 16 – Abathomphalus mayaroensis (Bolli), 15 – sample Gaj 5, 16 – sample Gaj 5.4. 17 – Globotruncanita
stuarti (de Lapparent), sample Gaj 5.4. 18, 20 – Globotruncana bulloides Vogler, sample Gaj 3. 19 – Globotruncana arca Cushman,
sample Gaj 5.7.
contusa and Globotruncana arca (species noted in the studied
assemblages) are characteristic of the transitional domain.
Malmgren (1991) stated that Abathomphalus mayaroensis,
Pseudotextularia elegans and Globotruncana arca character-
ize the so-called “warm transitional subassemblage”. Howev-
er, Malmgren also mentioned rugoglobigerinids among this
“subassemblage”, but they are absent in the studied material.
The compositions of the benthic foraminiferal assemblages
are also different than those of the Boreal province. For in-
stance, Stensioeina and Bolivinoides, genera characteristic for
the transitional zone are absent in the studied material. Kot-
larczyk (1978, 1985) listed such genera from the Wiar and
292
GASIŃSKI and UCHMAN
Fig. 9. Other microfossils from the Gaj section. 1 – Globotruncanita stuartiformis Dalbiez, sample Gaj 5.2. 2 – Globotruncana linneiana
(de Lapparent), sample Gaj 3. 3 – Globotruncana arca Cushman, sample Gaj 5. 4 – Aragonia ouezzensis (Rey), sample Gaj 5. 5 – Cibi-
cides sp., sample Gaj 5.4. 6 – Quadrimorphina allomorphinoides (Reuss), sample Gaj 5.4. 7 – Ostracoda, sample Gaj 5.4. 8 – ?Nodosa-
ria sp., sample Gaj 5.4A.
Leszczyny Members. However, the problem of migration pro-
cesses of microfauna between Tethyan Carpathian basins and
Boreal domain is still unsolved.
The connection between the Skole Basin and the adjacent
epicontinental sea has been suggested for quite some time.
Wawryk (1939) noted a similarity of the more or less coeval
sediments of the so-called Łopuszka Marls and Węgierka
Marls (about 20 km E of the studied section) to the marls ex-
posed near Lviv (the so-called Lviv Opoka). Kotlarczyk
(1988) mentioned that the Leszczyny Member marls resem-
ble the Upper Cretaceous marls from the Eastern European
Platform. These suggestions are confirmed by the studied
foraminiferal assemblage composition.
The possible migration gates of biota between the Boreal
and Tethyan provinces during the Late Cretaceous have been
discussed by Hanzliková (1972), Fuchs & Wessely (1996),
Gasiński (1998) and Marcinowski & Gasiński (2002). The
processes of migration and strategies of foraminiferal “mi-
grants” have been suggested by Gasiński (1997, 1998) and
Marcinowski & Gasiński (2002). In the later publication the
so-called “Lviv Gate” is suggested as the migration pathway
to the Carpathian basins from the North (Marcinowski &
Gasiński 1992, p. 109).
Conclusions
1. The studied deposits of the Ropianka Formation in the
Gaj section are here correlated with the Maastrichtian (part
of the Gansserina gansseri Zone and the Abathomphalus ma-
yaroensis Zone). The uppermost part of the section is dated
to the Paleocene. The K/T boundary is located within a 3 m
thick part of the Gaj section.
2. Foraminiferal assemblage composition indicates fluctu-
ations in organic matter flux to the marginal part of the Skole
Basin floor in the studied interval.
3. The studied foraminiferal assemblages are typical of the
“transitional zone” between the Tethyan and the Boreal do-
mains.
Acknowledgments: The authors greatly appreciate Janusz
Kotlarczyk (Academy of Mining and Metallurgy; Cracow) for
his constructive criticism and helpful remarks. We would like
to thank Michael A. Kaminski (University College London)
and Ryszard Marcinowski (Warsaw University) for their re-
viewer comments and suggesstions. Jagiellonian University
provided the support (DS funds).
References
Bieda F., Geroch S., Koszarski L., Książkiewicz M. & Żytko K.
1963: Stratigraphie des Karpates externes polonaises. Biul.
Inst. Geol. 181, 1—210.
Bromowicz J. 1974: Facial variability and lithological character of
Inoceramian Beds of the Skole Nappe between Rzeszów and
Przemyśl. Prace Geologiczne, Polska Akademia Nauk, Oddział
w Krakowie, Komisja Nauk Geologicznych 84, 1—83 (in Polish
with English summary).
Bukowy S. 1956: Observations on sedimentation of the Babica
clays (Palaeocene) in the Middle Carpathians. Bull. Polish
Acad. Sci. Cl. 3, 4(9), 631—635.
Bukowy S. 1957: Remarks on the sedimentation of the Babica
clays. Rocznik Polskiego Towarzystwa Geologicznego 26 (for
1956), 147—155 (in Polish).
Bukowy S. & Geroch S. 1957: On the age of exotic conglomerates
at Kruhel Wielki near Przemyśl (Carpathians). Ann. Soc. Geol.
Pol. 26, 297—329 (in Polish with English summary).
293
LATEST MAASTRICHTIAN FORAMINIFERAL ASSEMBLAGES (HUSÓW REGION, POLAND)
Burzewski W. 1966: Baculites marls on the lithostratigraphy back-
ground of the upper Inoceramian Beds of the Skiba Carpathians.
Zeszyty Naukowe AGH, Geol. 7, 89—115 (in Polish).
Caron M. 1985: Cretaceous planktonic foraminifera. In: Bolli H.M.,
Saunders J. & Perch-Nielesn K. (Eds.): Plankton stratigraphy.
Cambridge University Press, Cambridge, 17—86.
Friedberg W. 1900: Geological investigations of the vicinity of
Rzeszów and Łańcut. Kosmos 24, 289—311 (in Polish).
Friedberg W. 1901: Foraminiferids of the Inoceramian Beds of the
vicinity of Rzeszów and Dębica. Rozpr. Wydziału Matematyc-
zno-Przyrodniczego Akademii Umiejętności, Serya 3, Tom 1,
Dział B, Nauki Biologiczne 41, 601—668 (in Polish only).
Friedberg W. 1903: Geological Atlas of Galicia. Tekst do Zeszytu
Szesnastego. Wydawnictwa Komisyi Fizyograficznej Akademii
Umiejętności, Kraków, 1—147 (in Polish only).
Friedberg W. 1908: Small contribution to the Inoceramian Beds
fauna. Sprawozdanie Komisji Fizjograficznej Akademii Umie-
jetności 42, 58—63 (in Polish only).
Fuchs R. & Wessely G. 1996: The autochthonous Cretaceous at the
southern edge of the Bohemian Massif (Austria). In: Wessely
G. & Liebl (Eds.): Oil and gas in Alpine thrustbelts and basins
of Central and Eastern Europe. Geol. Soc. London, European
Assoc. Geosci. and Engineers, Spec. Publ. 5, 249—253.
Gasiński M.A. 1997: Tethyan-Boreal connection: influence on the
evolution of mid-Cretaceous planktonic foraminiferids. Creta-
ceous Research 18, 505—514.
Gasiński M.A. 1998: Campanian—Maastrichtian palaeoecology and
palaeobiogeography of the Andrychów Klippes, Outer Car-
pathians, Poland. Uniwersytet Jagielloński, Rozprawy Habili-
tacyjne 333, 1—90.
Gasiński M.A., Jugowiec M. & Ślączka A. 1999: Late Cretaceous
foraminiferids and calcareous nannoplankton from the
Węglówka Marls (Subsilesian Unit, Outer Carpathians, Po-
land). Geol. Carpathica 50, 1—11.
Gasiński M.A., Leśniak T. & Piotrowski M. 2001: Latest Maas-
trichtian foraminiferal Abathomphalus mayaroensis Zone in
the Subsilesian Unit (Polish Outer Carpathians). Bull. Polish
Acad. Sci., Earth Sci. 49, 89—97.
Gasiński M.A., Leśniak T. & Wróbel A. 2003: Biostratigraphy and
palaeoenvironmental analysis of the Żegocina Marls in the
Żegocina Tectonic Window (Subsilesian Unit, Polish Outer
Carpathians). Bull. Polish Acad. Sci., Earth Sci. 51, 1—9.
Gedl E. 1999: Lower Cretaceous palynomorphs from the Skole Nappe
(Outer Carpathians, Poland). Geol. Carpathica 50, 75—90.
Geroch S. & Kotlarczyk J. 1963: Remarks about the age of the Babice
Clay marls from the Bircza vicinity. Przegl. Geol. 11, 286—287
(in Polish).
Geroch S. & Nowak W. 1984: Proposal of zonation for the Late Ti-
thonian—Late Eocene based upon arenaceous foraminifera from
the Outer Carpathians, Poland. In: Oertli (Ed.): Benthos ’83:
2nd International Symposium on Benthic Foraminifera (Pau,
France). Elf-Aquitaine, ESSO REP and Total CFP, Pau & Bor-
deaux, 225—239.
Geroch S., Jednorowska A., Książkiewicz M. & Liszkowa J. 1967:
Stratigraphy based upon microfauna in the Western Polish
Carpathians. Biul. Inst. Geol. 211, 186—282.
Geroch S., Krysowska-Iwaszkiewicz M., Michalik M., Prochazka
K., Radomski A., Radwański Z., Unrug Z., Unrug R. & Wie-
czorek J. 1979: Sedimentation of the Wegierka marls. Ann.
Soc. Geol. Pol. 49, 105—133 (in Polish with English summary).
Gradstein F., Ogg J. & Smith A. 2004: A geologic time scale. Cam-
bridge University Press, Cambridge, 1—589.
Grzybowski J. 1903: Geological Atlas of Galicja. Tekst do Zeszytu
Czternastego. Wydawnictwa Komisyi Fizyograficznej Aka-
demii Umiejętności, Kraków, 1—91 (in Polish only).
Gucik S. 1962: Geology of the northern part of the Skole unit be-
tween Pruchnik and Ujkowice. Kwart. Geol. 4, 794—795 (in
Polish only).
Gucik S. 1987: Explanations to the Geological Map of Poland
1 : 50,000. Sheet Krzywcza. Wydawnictwa Geologiczne,
Warszawa, 1—77 (in Polish only).
Gucik S. & Wójcik A. 1982: Explanation to the Geological Map of
Poland 1 : 200,000. Sheet Przemyśl—Kalników. Wydawnictwa
Geologiczne, Warszawa, 1—91 (in Polish only).
Haczewski G. 1986: The place and role of marker lithological hori-
zons in litho- and chronostratigraphy. Przegl. Geol. 34, 247—250
(in Polish with English summary).
Hanzliková E. 1969: The Foraminifera of the Frydek Formation
(Senonian). Sbor. Geol. Věd 11, 7—84.
Hanzliková E. 1972: Carpathian Upper Cretaceous Foraminifera of
Moravia (Turonian—Maastrichtian). Rozpr. Ústř. Úst. Geol. 39,
1—160.
Hilber V. 1885: Randtheil der Karpathen bei Dębica, Ropczyce und
Łańcut. Jb. Geol. Reichsanst. 35, 407—428.
Jones R.W. & Charnock M. 1985: “Morphogroups” of agglutinated
foraminifera. Their life position and feeding habits and poten-
tial applicability in (paleo) ecological studies. Rev. Paleobiolo-
gie 4, 311—320.
Kaminski M.A. & Gradstein F.M. 2005: Atlas of Paleogene cosmo-
politan deep-water Foraminifera. Grzybowski Found. Spec.
Publ. 10, 1—547.
Kaminski M.A. & Kuhnt W. 1995: Tubular agglutinated foramin-
ifera as indicators of organic carbon flux. In: Kaminski M.A.,
Geroch S. & Gasiński M.A. (Eds.): Proceedings of the Fourth
International Workshop on Agglutinated Foraminifera. Grzy-
bowski Found. Spec. Publ. 3, 141—144.
Kollmann H.A. & Zapfe H. (Eds.) 1992: New aspects on Tethyan
Cretaceous fossil assemblages. Österr. Akad. Wiss. Schriften-
reihe der Erdwissenschaftlischen Kommissionen 9, 1—240.
Kotlarczyk J. 1978: Stratigraphy of the Ropianka Formation or of Inoc-
eramian Beds in the Skole Unit of the Flysch Carpathians. Prace
Geol., Polska Akad. Nauk, Oddział w Krakowie, Komisja Nauk
Geologicznych 108, 1—82 (in Polish with English summary).
Kotlarczyk J. 1979: Stratigraphy of the Ropianka Formation of the
Skole unit. Materiały Terenowej Konferencji Naukowej w Prze-
myślu, Przemyśl, 28—29 czerwca 1979 r. Sekcja Sedymentolo-
giczna Polskiego Towarzystwa Geologicznego, Kraków, 7—16
(in Polish).
Kotlarczyk J. 1985: An outline of the stratigraphy of marginal tec-
tonic units of the Carpathian Orogen in the Rzeszów-Przemyśl
area. In: Kotlarczyk J. (Ed.): Geotraverse Kraków—Baranów—
Rzeszów—Przemyśl—Ustrzyki Dolne—Komańcza—Dukla. Guide
to excursion 4. Carpatho-Balkan Geological Association XIII
Congress. Cracow, Poland 1985. Geol. Inst., Warszawa, 39—63.
Kotlarczyk J. 1988: Outline of the stratigraphy of the marginal tec-
tonic units of the Carpathian orogen In: Kotlarczyk J., Pękala K.
& Gucik S. (Eds.): Przewodnik 59 Zjazdu Polskiego Towarzyst-
wa Geologicznego, Karpaty Przemyskie, 16—18 września 1988.
Wydawnictwo AGH, Kraków, 23—62 (in Polish).
Kotlarczyk J., Jerzmańska A., Świdnicka E. & Wiszniowska T.
2007: A framework of ichtyofaunal ecostratigraphy of the Oli-
gocene-Early Miocene strata of the Polish Outer Carpathian
Basin. Ann. Soc. Geol. Pol. 76, 1—111.
Liszkowa J. 1956: Microfauna of the Subsilesian unit. Przegl. Geol.
10, 463—469 (in Polish).
Liszkowa J. & Morgiel J. 1981: Microfauna of the Frydek type in
Outer Carpathians, Poland. Biul. Inst. Geol. 331, 83—100 (in
Polish with English summary).
Malata T. 1996: An analysis of formal lithostratigraphic divisions
and a proposition of the subdivision of the Skole Unit of the Pol-
ish Flysch Carpathians. Przegl. Geol. 44, 509—514 (in Polish).
Malata T. 2001: The Skole Unit east of Rzeszów. Posiedzenia
294
GASIŃSKI and UCHMAN
Naukowe Państwowego Instytutu Geologii, 57(9), 60—63 (in
Polish).
Marcinowski R. & Gasiński M.A. 2002: Cretaceous biogeography
of epicratonic Poland and Carpathians. In: Michalík J. (Ed.):
Tethyan/Boreal Cretaceous Correlation. Mediterranean and
Boreal Cretaceous paleobiogeographic areas in Central and
Eastern Europe. Veda, Publishing House of the Slovak Acade-
my of Sciences, Bratislava, 95—115.
Morgiel J. & Żgiet J. 1961: Upper Cretaceous deposits at Dydynia
borehole (Sanok Carpathians). Kwart. Geol. 5, 993—994 (in
Polish).
Nederbragt A.J. 1991: Late Cretaceous biostratigraphy and develop-
ment of Heterohelicidae (planktic foraminifera). Micropaleon-
tology 37, 329—372.
Olsson R.K. & Nyong E.E. 1984: A paleoslope model for Campa-
nian—lower Maestrichtian foraminifera of New Jersey and Del-
aware. J. Foram. Res. 14, 50—69.
Olsson R.K. & Wise S.W. 1987: Upper Maastrichtian to middle
Eocene stratigraphy of the New Jersey slope and coastal plain.
In: van Hinte J.E., Wise S.W. et al. (Eds.): Initial Reports of
the Deep Sea Drilling Project 93, 1243—1365.
Olsson R.K., Hemleben C., Berggren W.A. & Huber B.T. 1999: At-
las of Paleocene planktonic foraminifera. Smithsonian Contri-
butions to Paleobiology 85, 1—252.
Paul K.M. 1869: Die geologischen Verhaltnisse des nördlichen Sa-
roser and Zempliner Comitates. Jb. K.-Kön. Geol. Reichsanst.
19, 156—280.
Premoli-Silva I. & Rettori R. (Eds.) 2002: Practical manual of Cre-
taceous planktonic Foraminifera. International School on
Planktonic Foraminifera, Perugia 18—22 February, 2002. Di-
partimento di Scienza della Terra, Universita di Perugia, Pe-
rugia, 1—462.
Premoli-Silva I. & Verga D. 2004: Practical manual of Cretaceous
planktonic Foraminifera. International School on Planktonic
Foraminifera. 3
0
Course: Cretaceous. Verga et Rettori eds.
Universites of Perugia and Milano, Tipografia Pontfelcino,
Perugia, 1—283.
Rajchel J. 1990: Lithostratigraphy of the Upper Paleocene and
Eocene deposits in the Skole Unit. Zeszyty Naukowe AGH,
Geol. 48, 1—112 (in Polish with English summary).
Rajchel J. & Uchman A. 1998: Ichnological analysis of an Eocene
mixed marly-siliciclastic flysch deposits in the Nienadowa
Marls Member, Skole Unit, Polish Flysch Carpathians. Ann.
Soc. Geol. Pol. 68, 61—74.
Robaszynski F. & Caron M. 1995: Foraminiferes planctoniques du
Crétacé: commentaire de la zonation Europe-Méditerrané.
Bull. Soc. Géol. France 6, 681—692.
Robaszynski F., Caron M., Gonzales J.M. & Wonders A.H. (Eds.)
1984: Atlas of Late Cretaceous globotruncanids. Rev. Micro-
paleontologie 26, 145—305.
Scheibnerova V. 1971: Foraminifera and the Mesozoic biogeoprov-
inces. Geol. Surv. New Soth Wales 13, 135—174.
Sliter W.V. 1972: Upper Cretaceous planktonic foraminiferal zoo-
geography and ecology-eastern Pacific margin. Palaeogeogr.
Palaeoclimatol. Palaeoecol. 12, 15—31.
Sliter W.V. & Baker R.A. 1972: Cretaceous bathymetric distribu-
tion of benthic foraminiferids. J. Foram. Res. 2, 167—183.
Szymakowska F. 1961: A new locality with “Palaeocene” sediments
from the Skole Unit at Kamienica Dolna and Gorzejowa (Car-
pathians). Kwart. Geol. 5, 613—629 (in Polish with English
summary).
Ślączka A. & Kaminski M.A. 1998: A guidebook to excursions in
the Polish Flysch Carpathians. Grzybowski Found. Spec. Publ.
6, 11—71.
Ślączka A. & Miziołek M. 1995: Geological setting of Ropianka
Beds in Ropianka (Polish Carpathians). Ann. Soc. Geol. Pol.
65, 29—41.
Tietze E. 1883: Beiträge zur Geologie von Galizien. Jb. K.-Kön.
Geol. Reichsanst. 33, 443—560.
Tshakreen S.O. & Gasinski M.A. 2004: Cretaceous-Paleogene
boundary problem in Libya: the occurrence of the foraminifer-
al species Abathomphalus mayaroensis (Bolli) in the Western
Sirt Basin. Geol. Quart. 48, 77—82.
Uhlig V. 1888: Ergebnisse geologischer Aufnahmen in den westgal-
izischen Karpathen. I. Theil. Die Sandsteizone zwischen dem
penninischen Klippenzuge und dem Nordrande. Jb. K.-Kön.
Geol. Reichsanst. 38, 83—264.
Vialov O.S., Dabagian N.W. & Zhurakovsky A.G. 1967: Description
of the Cretaceous Flysch section along the Dniestr river between
Tershevo and Spas. Geol. J. 27, 3—15 (in Ukrainian).
Wawryk W. 1930: L’analyse petrographique de la marne de Lwów
et des marnes de Łopuszka et de Węgierka. Kosmos A, 54,
889—915 (in Polish with French summary).
Wdowiarz S. 1936: Report of geological investigations in the Car-
pathians in 1936 in the area of SE from Rzeszów. Spraw.
Państw. Inst. Geol. 45, 20—22 (in Polish).
Wdowiarz S. 1949: Structure géologique des Karpates Marginales
au sud-est de Rzeszów. Biul. Państw. Inst. Geol. 11, 1—51.
Wdowiarz S., Wieser T., Szczurowska J., Morgiel J. & Szotowa W.
1974: Geological structure of the Skole unit and its basement
in the column of the Cisowa IG 1 Borehole. Biul. Inst. Geol.
18, 1—94 (in Polish with English summary).
Zhurakovsky A.G. 1971: Stratigraphy of the Cretaceous deposits of
the northern slope of the Ukrainian Carpathians. Materialy po
Geologii i Neftegazonosnosti Ukrainy 26, 85—96 (in Russian).
Żytko K. & Zimnal Z. 1997: Explanations to the Geological Map of
Poland 1 : 50,000. Sheet Ustrzyki Dolne. Wydawnictwa Geo-
logiczne, Warszawa, 1—44 (in Polish).