Kaminski PDF

Marine Geology 190 (2002) 165^202
www.elsevier.com/locate/margeo
Late Glacial to Holocene benthic foraminifera in the

Marmara Sea: implications for Black Sea^Mediterranean Sea
connections following the last deglaciation
Michael A. Kaminski a;b; , Ali Aksu c , Matthew Box a;b , Richard N. Hiscott c ,
Sorin Filipescu a;b;d , Muna Al-Salameen a;b
a
Research School of Geological and Geophysical Sciences, University College London, Gower Street, London WCIE 6BT, UK
b
KLFR, 3 Boyne Avenue, Hendon NW4 2JL, UK
c
Department of Earth Sciences, Memorial University of Newfoundland, St. Johns, NF, Canada A1B 3X5
d
Department of Geology, Babes-Bolyai University, Kogalniceanu 1, RO-3400, Cluj-Napoca, Romania
Received 25 May 2001; accepted 19 February 2002
Abstract
Benthic foraminifera were studied from four gravity cores that penetrated Holocene marine sediments in the
Marmara Sea. Morphogroup and assemblage analyses reveal that the Holocene sea-level rise did not result in a
catastrophic flooding event as proposed by W.B.F. Ryan and others, whereby well-oxygenated, saline Mediterranean
waters rapidly inundated a low-lying low salinity Black Sea Lake at V7.15 ka (popularly known as the Noahs
Flood Hypothesis). Rather, the benthic foraminiferal data confirm the hypothesis that the Dardanelles sill was
breached by the Mediterranean at V12 ka, allowing saline waters to penetrate the Marmara Sea. These saline waters
reached the level of the Bosphorus sill at V9.5 ka, but were unable to penetrate into the Black Sea until after V9.1
ka because of the persistent strong outflow of brackish to fresh water from the Black Sea. The initial colonisation of
the Marmara Sea by benthic foraminifera is essentially synchronous with the re-establishment of marine connections
through the Dardanelles Strait at V12 ka. By V10 ka, Ammonia-dominated faunas developed on the strait-exit delta
(v1) at the southern end of the Bosphorus, and at V9.1 ka the appearance of fully marine species documents the
establishment of a more stratified water column over v1. Finally, the increase in abundance of planktonic
foraminifera at the southern exit of the Bosphorus after V6.1 ka reflects a decreased volume of outflow water from
the Black Sea. Quantitative analysis of benthic foraminiferal morphogroups reveals that the oxygen content of subhalocline water was low (below V1.5 ml/l) throughout the Holocene, and the occurrence of sapropel sediment in the
deeper part of the basin suggests bottom waters may have been anoxic at times. After V4.5 ka, an increase in benthic
foraminiferal oxic morphotypes suggests a reduction in Black Sea outflow and weakening of the halocline. The strong
and persistent stratification of the water column in the Marmara Sea throughout the Holocene is entirely
incompatible with the Noahs Flood Hypothesis.
: 2002 Elsevier Science B.V. All rights reserved.
Keywords: Marmara Sea Gateway; Black Sea; Holocene; benthic foraminifera
* Corresponding author.
E-mail address: m.kaminski@ucl.ac.uk (M.A. Kaminski).
0025-3227 / 02 / $ ^ see front matter : 2002 Elsevier Science B.V. All rights reserved.
PII: S 0 0 2 5 - 3 2 2 7 ( 0 2 ) 0 0 3 4 7 - X
MARGO 3162 4-10-02
166
M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202
Fig. 1. Core locations (black circles) in the Marmara Sea. Bathymetry is from Aksu et al. (2000)
1. Introduction
The Marmara Sea occupies a transtensional basin situated along a set of en echelon dextral
strike-slip faults that form part of the North Anatolian Transform Fault system (Aksu et al., 2000).
It is a critical oceanographic gateway connecting
the Aegean Sea, to the west, and the Black Sea, to
the northeast, and serves as the only link between
the Black Sea and the Mediterranean. Two relatively shallow and slender straits, the Dardanelles
and the Bosphorus, connect the Marmara Sea to
the Aegean and Black seas, respectively (Fig. 1).
Even though the Dardanelles strait reaches depths
of 100^110 m, several sills are present to contemporary depths of 60^70 m. These sills prevent the
exchange of deep water between the Aegean Sea
and the Black Sea (Ergin et al., 1997). Today,
brackish surface water exits the Black Sea
through the Bosphorus strait, while saline deeper
water from the Marmara Sea ows northward as
a countercurrent. An identical two-way ow exists
in the Dardanelles Strait, thereby establishing an
overall estuarine circulation within the Marmara
Sea. Because of the existence of brackish Black
Sea outow water, a strong halocline is present
throughout the Marmara Sea, leading to low-oxygen conditions below a thin well-mixed surface
layer.
During the last glacial maximum, global sea
level was V120 m below its present level (Fairbanks, 1989), and the Marmara Sea (as well as the
Black Sea) was isolated from the Mediterranean.
During the last deglaciation as sea level rose to ca.
370 m, a marine connection was rst established
with the Mediterranean through the Dardanelles.
As sea level rose to the depth of the Bosphorus sill
(340 m), an eective marine connection was eventually established with the Black Sea once twoway ow developed (Lane-Ser et al., 1997).
This two-way ow required a sucient depth of
water in the strait and a reduction of the earlier
strong outow of Black Sea surface water to the
point where Mediterranean saline water could
penetrate along the full length of this waterway.
The development of a marine connection between the Black Sea and Mediterranean during
the early Holocene would have had a profound
inuence on the biotic record of the intervening
Marmara Sea. In recent years, a much-publicised
controversy has emerged concerning the timing
and development of marine connections to the
MARGO 3162 4-10-02
Black Sea following the last deglaciation. On the

one hand, geochemical studies of the youngest
sapropel horizon (S1, V9.5^6.4 ka) in the Aegean
Sea (Aksu et al., 1995, 1999) and a partly contemporaneous sapropel in the deep Marmara Sea
(V10.6^6.4 ka; CMagatay et al., 2000; Aksu et
al., 2002a) suggest a strong outow of low-salinity
water from the Black Sea beginning at V10.5 ka.
The presence of a strait-exit delta with an age of
V10^9 ka at the southern end of the Bosphorus
Strait supports the timing of this outow (Hiscott
et al., 2002). On the other hand, Ryan et al.
(1997) cited sedimentological and faunal evidence
from the northern Black Sea that in their opinion
points to the catastrophic inundation of the Black
Sea by water of Mediterranean origin at
V7.15 ka, spawning the Noahs Flood Hypothesis (Ryan and Pitman, 1998). More recent studies suggest a more gradual transgression of the
Black Sea shelves, beginning no later than
V11 ka (Gorur et al., 2001; Aksu et al., 2002b).
Micropalaeontological studies of the Holocene
sediment in the Marmara Sea may be instrumental in resolving this debate. If, as the studies of
sapropels suggest, a two-way ow and a strongly
stratied water column had been established by
V10.5 ka, benthic foraminiferal assemblages
from the Marmara Sea should reect low-oxygen
conditions. However, if the scenario discussed by
Ryan et al. (1997) is correct and a rapid unidirectional ow of marine surface waters into the
Black Sea through the Bosphorus Strait had taken
place at V7.15 ka, marine organisms of Mediterranean origin would have been swept into the
Marmara Sea at that time by the strong ooding
currents. Moreover, the stable density stratication of the Marmara Sea would have been disrupted, resulting in a well-oxygenated water column. Initial studies of Holocene sediments and
fauna from the Marmara Sea (Algan et al.,
2001) strongly support the existence of persistent
dysoxic conditions below a stable halocline, contrary to the expected conditions during a rapid
inundation.
The objectives of this study are to (1) provide a
taxonomic census of the benthic foraminifera in
gravity cores collected from a range of water
depths in the Marmara Sea, (2) more fully inves-
167
tigate the history of the marine connections between the Black Sea and Mediterranean, (3) trace
the development of oxygen depletion beneath the
pycnocline, and (4) distinguish between the conicting hypotheses regarding the timing of marine
connections using quantitative analysis of benthic
foraminiferal assemblages.
2. Previous studies
Benthic foraminifera from the Eastern Mediterranean have been studied by Cimerman and
Langer (1991), who produced a workable taxonomic framework for the region. This framework
has been expanded by faunal studies of the Gulf
of Naples, Italy by Sgarrella and Moncharmont
Zei (1993). Black Sea foraminifera have been
documented by Yanko and Troitskaja (1987),
and their ecology summarised by Yanko (1990).
The only published studies of foraminifera from
the Marmara Sea are (1) the work of Alavi (1988),
who examined two sediment cores collected from
a depth of 1200 m in the deep basin south of
Istanbul, and (2) descriptions of upper Pliocene
to Holocene foraminifera from geotechnical boreholes in the Gulf of Izmit (MericM et al., 1995).
Alavi (1988) found the foraminifera in the upper
metre of the marine sediment column to consist
mostly of infaunal forms that are known from
oxygen-decient environments rich in organic
matter, and noted faunal similarities to older sapropel layers exposed on land in other areas of the
Mediterranean. Alavi (1988) concluded that these
sediments were deposited subsequent to the establishment of an estuarine circulation in the Marmara Sea, but owing to the lack of absolute age
determinations, he was unable to provide a chronology for his cores. In addition to the work of
MericM et al. (1995), shallow-water benthic foraminifera have been recently studied from Iskundrun
Bay on the Mediterranean coast of Turkey (Basso
and Spezzaferri, 2000). This study provides calibration of the depth ranges of neritic benthic foraminifera in this sector of the Mediterranean,
and many of the same species are found in our
sediment cores (see below). Unfortunately, little is
known about the depth distribution of modern
MARGO 3162 4-10-02
168
benthic foraminifera within the Marmara Sea itself.
3. Methods
In this paper, we document the benthic foraminifera from four cores collected during the
MAR97 and MAR98 cruises of the R/V Koca
Piri Reis of the Institute of Marine Sciences and
Technology, Dokuz Eylul University, Izmir, Turkey (Fig. 1). The sediments were collected using a
4-m-long corer with 10 cm internal diameter and
400 kg weight. Two of the cores (MAR98-7 and
MAR98-9) were collected from the Holocene delta on the northern Marmara Sea shelf near the
southern exit of the Bosphorus (Hiscott et al.,
2002). A third core (MAR97-11) was studied
form the southern Marmara Sea shelf, and a
fourth (MAR98-12) penetrated a sapropel in the
deeper part of the Marmara Sea. The sedimentology and depositional history at these core locations are described in detail by Hiscott et al.
(2002) and Hiscott and Aksu (2002), while geochemistry and water mass history are discussed by
Aksu et al. (2002a,c). Details of the cores are
given in Table 1 ; they are currently curated at
the Department of Earth Sciences, Memorial University of Newfoundland. Standard 10-cm3 samples were collected at 10-cm intervals from the
working half of the four cores. Samples were disaggregated by boiling in a 1% Calgon solution,
and wet-sieved over a 63-Wm sieve. Foraminifera
were picked out of the s 125-Wm fraction, and
mounted on cardboard microscope slides, housed
in the Kaminski Collection at the Department of
Geological Sciences, University College London.
Selected specimens were photographed using a
Table 1
Core locations and water depths
Core number
Latitude
(N)
Longitude
(E)
Water depth
(m)
MAR97-11
MAR98-7
MAR98-9
MAR98-12
4039.20P
4050.98P
4055.36P
4050.54P
2822.67P
2900.98P
2856.80P
2747.68P
111
95
64
549
Zeiss-940 digital scanning electron microscope at

UCL.
In this study, we utilise the Benthic Foraminiferal Oxygen Index (BFOI) originally developed by
Kaiho (1991). The BFOI was originally based on
benthic foraminiferal data from DSDP cores from
the Pacic, South Atlantic and Indian oceans. Using oxic and dysoxic morphotypes originally determined by Bernhard (1986), Kaiho (1991) divided benthic foraminifera into three main groups
according to test morphology: (1) the anaerobic
forms were dened as those with small- to medium-sized tests with a high surface area to volume ratio, and elongate-attened, tapered, and
cylindrical morphotypes, and with thin, unornamented, porous test walls; (2) the aerobic forms
are those with low surface area to volume ratio,
and spherical, planoconvex, and lenticular morphologies with thick test walls (3) the intermediate or suboxic forms were those similar to
anaerobic forms but possessing thick or ornamented test walls, such as costate Uvigerina and
Bulimina, Nodosaria, and Stilostomella. Also included were this lenticular and planispiral forms
characterised by medium surface area to volume
ratios and thin walls. Kaiho (1994) further divided suboxic indicators into three groups, A, B, and
C. Group A comprises small specimens ( 6 350 Wm)
of oxic species able to live in less oxygenated conditions because of their size. Group B consists of
species that are considered to be between the morphological extremes of the oxic and dysoxic indicators. These include Lenticulina, large Nodosaria,
Dentalina, and large ornamented species of Bulimina; rounded planispiral, at ovoid and spherical forms; small and/or thin-walled, planoconvex
and biconvex trochospiral forms; and Uvigerina,
Gyroidina, Gyroidinoides, and Hoeglundina. Species of group B contain both epifaunal dwellers
and infaunal dwellers under high-oxygen conditions that are epifaunal faunal dwellers in lowoxygen conditions. Group C indicators are those
species that have thin walls but are considered to
have a microhabitat between those of group B and
dysoxic indicators, these taxa include Bulimina
aculeata, Nonionella spp., and Elphidium excavatum. In this study, we used the oxic, suboxic, and
dysoxic morphogroups dened by Kaiho (1994).
MARGO 3162 4-10-02
Kaihos (1991, 1994) BFOI is an empirical ratio

of dysoxic and oxic forms which was dened as:
a=a nU100
where a is the number of oxic species and n the
number of dysoxic species. When a = 0 and
n+s s 0 (s is the number of suboxic indicators)
then the BFOI value is given by [(s/(s+n)31]U
50. In the latter study, Kaiho (1994) calibrated
the modern values of the BFOI to levels of dissolved oxygen in bottom waters in the modern
ocean. Three main BFOI value divisions are dened by Kaiho (1994) : oxic BFOI values, which
range from 100 to 0, represent dissolved oxygen
conditions of s 1.2 ml/l; suboxic BFOI values,
ranging from 0 to 340, represent dissolved oxygen values of between 1.3 and 0.3 ml/l; and dysoxic BFOI values, which range from 340 to 355,
represent dissolved oxygen levels of between 0.3
and 0.1 ml/l. Black laminated mud and shale barren of calcareous benthic foraminifera but containing planktonic foraminifera are assigned a
BFOI value of 6 355.
Kaiho (1999) re-evaluated his BFOI with respect to organic carbon ux, temperature, and salinity. He analysed calcareous benthic foraminifera from core tops at 73 oceanic sites and
calculated the BFOI values for each site. Kaiho
found that correlation coecients between productivity, organic carbon ux, and dissolved oxygen level (R2 = 0.36^0.51) were much lower than
those between dissolved oxygen levels and BFOI
values (R2 = 0.78 and 0.81). This study demonstrated the usefulness of the BFOI as a proxy
for bottom-water dissolved oxygen content, especially over the range of values observed in the
Marmara Sea.
4. Results
4.1. Taxonomy
A total of 117 species of benthic foraminifera
were found in the studied Marmara Sea cores.
Foraminifera are abundant in the Holocene mud
drape. The recovered assemblages display strong
169
anities to those described from the modern

Mediterranean Sea but are lower in diversity,
being poor in groups such as larger foraminifera
and organically cemented agglutinated foraminifera. The taxonomic classication of benthic foraminifera recovered from our studied cores is outlined in Appendix 1. Representative specimens are
illustrated in Plates I^V.
4.2. The Bosphorus Strait-exit delta
Core MAR98-9 was collected from a water
depth of 64 m on the outer shelf, just south of
the exit of the Bosphorus Strait. Major lithological boundaries are observed at 55 cm and 110 cm
in the core. The uppermost unit is interpreted to
represent a transgressive to highstand marine
drape (Hiscott et al., 2002), and radiocarbon
dates constrain its age to V9.0^0 ka. The sediment below 55 cm contains increasing amounts of
sand with depth, and is interpreted as the distal
equivalent of a prograding lobate delta located
south of the exit of the strait (v1 of Hiscott et
al., 2002). Radiocarbon dates give an age of 10^
9 ka for this interval. v1 is unusual in that it was
not sourced from a river, but from a strait linking
two small seas when one sea (the Black Sea) was
owing vigorously into the other (see below).
Benthic foraminiferal assemblages in the core
(Fig. 2 ; Appendix 2) reect a history of increasing
water depth through time, as Holocene sea level
rose and the site became increasingly more marine. Foraminifera at the base of the core (120
cm) are abundant, display low diversity, and are
highly dominated by Ammonia spp. Textularia
spp. and Elphidium spp. are also present. This
impoverished assemblage (radiometrically dated
at 10 220 yr BP at 113 cm) is interpreted as reecting shallow-water conditions and low salinity.
Between 110 and 55 cm, the diversity of benthic
foraminifera increases upcore, and the rst occurrences of Aubignyna perlucida, Porosononion martkobi, Nonionella opima, Bulimina spp., Brizalina
spp., Fursenkoina acuta, and Lobatula lobatula
are observed. Planktonic foraminifera are absent
in this interval. This change from an Ammoniadominated assemblage to a more diverse one coincides with an upwards increase in the amount of
MARGO 3162 4-10-02
170
Plate I.
MARGO 3162 4-10-02
silt and clay, and reects increasing water depths

and drowning of v1. This faunal change is constrained by radiometric dates of 9840 yr BP at
94 cm and 9070 yr BP at 60 cm.
At 40 cm, planktonic foraminifera become common, and Ammonia disappears from the record
entirely. Instead, an assemblage dominated by infaunal forms such as Brizalina and Bulimina suggests deposition beneath a stratied water column
(radiometrically dated at 6120 yr BP at 42 cm).
Core MAR98-7 was collected near the shelf
edge at a depth of 95 m. During the last Glacial
lowstand, the water level in the Marmara Sea was
90^100 m lower than it is today, so this site would
have been near the shoreline of the Marmara
Lake (Aksu et al., 1999). Below 70 cm in the
core, the fresh- to brackish-water mollusc Dreissena rostiformis distincta is observed (Hiscott et
al., 2002). Benthic foraminifera are very sparse,
but are consistently present to the base of the
core (Fig. 3; Appendix 2). The occurrence of
Haynesina depressa, Aubignyna perlucida, and
Ammonia compacta, species that are rare in the
overlying marine unit, suggests either reworking
from older strata, or that a relict fauna may
have been present in the Marmara Sea during
glacial times. Radiocarbon dates from this interval give an age in excess of 40 ka.
At 70 cm in the core, an abrupt change in the

numbers and diversity of benthic foraminifera is
observed. The assemblage recovered from 70^
60 cm is dominated by Bulimina spp., Brizalina
spp., Cassidulina carinata, and Nonionella opima,
indicating that marine conditions were rapidly established. No shallow-water Ammonia-dominated
assemblage was observed at the base of this marine interval, which supports the idea of rapid
ooding when the Dardanelles was breached.
Higher in the core, the proportions of C. carinata
and N. opima decrease, and Bulimina, Polymorphina, Biloculinella, and Hyalinea increase, reecting
deeper marine conditions in a permanently stratied water column.
4.3. Southern Marmara Sea shelf
Core MAR97-11 was collected from a water
depth of 111 m on the southern Marmara Sea
shelf, in the toeset of the most seaward lowstand
delta of oxygen isotopic stage 2. The core locality
was in a permanently subaqueous part of the basin, and therefore records the history of palaeoenvironmental conditions during the last lowstand
as well as the marine invasion of the Marmara
Sea after the breaching of the Dardanelles Strait.
Below a core depth of 100 cm, only the mollusc
Plate I.
1.
2.
3.
4a.
4b.
5.
6a.
6b.
7.
8a.
8b.
9.
10.
11.
12.
13.
14.
Textularia bocki Hoglund, 1947

Textularia bocki Hoglund, 1947
Spirorutilus sp
Spirorutilus sp
Spirorutilus sp
Textularia cushmani Said, 1949
Textularia sp
Textularia sp
Textularia sp
Bigenerina nodosaria dOrbigny, 1826
Spiroloculina tenuiseptata Brady, 1884
Spiroloculina excavata dOrbigny, 1846
Adelosina cliarensis (Heron-Allen and
Earland, 1930)
Adelosina cliarensis (Heron-Allen and
Earland, 1930)
Adelosina sp
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
171
^
^
^
^
^
^
^
^
^
^
^
^
^
^
^
10 cm
10 cm
50 cm
50 cm
50 cm
50 cm
50 cm
50 cm
50 cm
50 cm
50 cm
0 cm
10 cm
40 cm
80 cm
Side view U90

Side view U95
Side view U95
Side view U150
Apertural view U170
Side view U90
Side view U90
Pseudopores U1200
Side view U145
Side view U300
Side view U300
Side view U130
Side view U150
Side view U150
Side view U120
Core MAR97-11 ^ 80 cm
Side view U180
Core MAR97-11 ^ 80 cm
Side view U100
MARGO 3162 4-10-02
172
Plate II.
MARGO 3162 4-10-02
Dreissena rostriformis distincta is present. Benthic

foraminifera (Fig. 4 ; Appendix 2) are either absent or are represented by very rare specimens
that could have been reworked from older strata
and/or downmixed by burrowers or by the coring
process. Radiometric dates of 14 970 yr BP at
174 cm and 12 970 yr BP at 92 cm pre-date the
breaching of the Dardanelles Strait, and therefore
correspond to a time when lowstand deltas were
still active along the southern shelf of the Marmara Sea (Aksu et al., 1999).
At V80 cm, benthic foraminifera suddenly become abundant (Fig. 4). The assemblage at this
depth is comprised mostly of Textularia spp., Cassidulina carinata, Haynesina depressa, Aubignyna
perlucida, and Fursenkoina acuta. Both F. acuta
and C. carinata display the behaviour of pioneering species which can initially colonise a barren
substrate in large numbers. Their relative abundance then decreases upcore as the diversity of
the fauna increases. A maximum of Nonionella
opima is observed from 60 to 40 cm. At 40 cm,
an increase in the relative abundance of Brizalina
spp. and Bulimina spp. is observed. At 30 cm,
there is an increase in the abundance of Discorbinella bertheloti, while Hyalinea balthica and Textularia spp. increase at 20 cm. A radiometric age
of 10 790 yr BP at 79 cm clearly documents that
the drowning of the delta and the rapid transition
to a fully marine fauna occurred when global sea
level stood V65^70 m lower than today. This
173
elevation coincides with the modern depth of the

bedrock sills in the Dardanelles Strait. Following
the initial rapid transition, additional marine
species from the Mediterranean then gradually
colonised the deeper shelf as sea level continued
to rise.
4.4. Deep Marmara Sea
The deepest locality studied is Core MAR98-12,
recovered from a present-day water depth of
549 m. Samples from the basal section of the
core are barren of foraminifera. At 130 cm at
the base of sapropel M1 (radiocarbon date of
10 660 yr BP), a bloom of Fursenkoina accompanied by a few specimens of Brizalina and Bulimina
is observed. The entry of these marine species
documents the establishment of marine connections between the Marmara Sea and the Aegean
Sea. Samples collected from the sapropel layer
itself are barren of foraminifera, or contain just
a few specimens of Chilostomella, Bolivina, and
Brizalina which may have been downmixed. Conditions during the deposition of the sapropel at
this locality must have been anoxic at times.
Near the top of the sapropel layer at 90 cm, a
maximum in Globobulimina is observed, indicating
a slight improvement in the bottom water oxygenation. At 80 cm, miliolids and Hyalinea appear,
while Uvigerina makes its rst appearance at
20 cm, suggesting further increase in oxygenation.
Plate II.
1.
2a.
2b.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
Biloculinella globula (Bornemann, 1855)

Quinqueloculina patagonica dOrbigny, 1839
Quinqueloculina stelligera Schlumberger, 1893
Lagena striata (dOrbigny, 1839)
Amphicoryna proxima (Silvestri, 1872)
Lenticulina gibba (dOrbigny, 1826)
Homalohedra sp
Favulina hexagona (Williamson, 1848)
Brizalina spathulata (Williamson, 1858)
Brizalina striatula (Cushman, 1922)
Brizalina catanensis (Seguenza, 1862)
Brizalina alata (Seguenza, 1862)
Brizalina dilatata (Reuss, 1850)
Brizalina sp
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MARGO 3162 4-10-02
^
^
^
^
^
^
^
^
^
^
^
^
^
^
^
40 cm
40 cm
40 cm
10 cm
10 cm
20 cm
50 cm
10 cm
80 cm
30 cm
0 cm
0 cm
20 cm
30 cm
30 cm
Oblique side view U500

Side view U90
Apertural view U500
Side view U90
Side view U130
Side view U150
Side view U240
Side view U300
Side view U310
Side view U115
Side view U150
Side view U175
Side view U90
Side view U140
Side view U150
174
Plate III.
MARGO 3162 4-10-02
5. Discussion
5.1. Initial recolonisation of the Marmara Sea
after the last deglaciation
Three of the studied cores recovered the base of
the upper marine layer that drapes the lowstand
deltas on the Marmara Sea shelf. Radiocarbon
dates at the two deeper sites (MAR98-12 and
MAR97-11) are consistent with the V12-ka estimate for the breaching of the Dardanelles sill
(Aksu et al., 2002a). At that time, Mediterranean
Sea water began to ow into the Marmara Lake
from the Aegean Sea. Among the rst species to
establish themselves at the deeper localities in the
Marmara Sea were Aubignyna perlucida, Cassidulina carinata, Haynesina depressula, and Fursenkoina acuta. In Iskundrun Bay, H. depressula occurs at water depths as shallow as 9 m (Basso and
Spezzaferri, 2000), while Fu. acuta is known from
the littoral zone in the northern Adriatic (Iaccarino, 1967, reported in Sgarrella and Moncharmont Zei, 1993). This initial recolonisation event
documents the rst signicant inux of Mediterranean surface waters through the Dardanelles
after the last deglaciation (benthic foraminifera
recovered from Pliocene and older Pleistocene
sediments in the Gulf of Izmet by MericM et al.,
1995 point to previous periods of faunal connections with the Mediterranean). The Dardanelles,
however, apparently acted as a selective faunal
lter, as we do not observe any of the larger rotaliids and miliolids that are common at shallow
175
depths in the eastern Mediterranean. Rare (and

stunted) specimens of Planorbulina mediterranensis constitute the only larger foraminifera in our
samples. It is quite possible that the larger foraminifera have been excluded because of the low
salinity of the upper 20 m of the water column.
This initial recolonisation event was followed
by an increase in Brizalina and Bulimina, which
is observed at all studied localities. These forms
have a wide bathymetric range, but on average
occur at deeper stations in Iskundrun Bay (Basso
and Spezzaferri, 2000). At a later stage in the
recolonisation, species such as Hyalinea balthica
appear in our cores. This species lives below 70
m depth in the Gulf of Naples (Sgarrella and
Moncharmont Zei, 1993), and its appearance in
the Marmara Sea reects the deepening of water
over the Dardanelles sill as sea level rose further
during the later Holocene.
The selective lter eect of the Dardanelles sill
is still in evidence today, since deep stations in the
Marmara Sea are poor in organically cemented
deep-water agglutinated foraminifera and cosmopolitan bathyal benthics such as Pullenia and
Melonis. These forms are present in the Aegean
Sea, but because they possess upper depth limits
that are deeper than the Dardanelles sill, they
have not been able to enter the Marmara Sea.
5.2. Drowning of the Bosphorus Strait-exit delta
The location of Core MAR98-9 was chosen to
decipher the history of the Holocene delta (v1) at
Plate III.
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
Cassidulina carinata Silvestri, 1896

Cassidulina carinata Silvestri, 1896
Bulimina aculeata dOrbigny, 1826
Bulimina elongata dOrbigny 1846
Bulimina costata dOrbigny, 1852
Bulimina costata dOrbigny, 1852
Bulimina sp
Globobulimina anis (dOrbigny, 1839)
Rectiuvigerina phlegeri Le Calvez, 1959
Uvigerina mediterranea Hofker, 1932
Fursenkoina acuta (dOrbigny, 1846)
Fursenkoina acuta (dOrbigny, 1846)
Hyalinea balthica (Schroeter, 1783)
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MARGO 3162 4-10-02
^
^
^
^
^
^
^
^
^
^
^
^
^
70
70
30
10
30
30
30
20
70
10
70
70
30
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
Side view U155

Apertural view U250
Side view U100
Side view U160
Side view U120
Side view U150
Side view U135
Side view U80
Side view U90
Side view U55
Apertural view U160
Side view U160
Umbilical view U95
176
Plate IV.
MARGO 3162 4-10-02
the southern entrance of the Bosphorus, and by

inference the history of outow from the Black
Sea. Here, the presence in seismic proles of a
southward-prograding delta is interpreted as evidence for a strong unidirectional outow current
from the Black Sea (Hiscott et al., 2002). The
presence of brackish Ammonia-dominated faunas
within deltaic sediments at the base of Core
MAR98-9, dated radiometrically at V10.2 ka, is
here interpreted as evidence of this freshwater
outow from the Black Sea. On the modern Black
Sea shelf, foraminiferal faunas with s 80% Ammonia characterise very shallow deltaic or lagoonal environments with salinities below 5x (Yanko, 1990). Using the known sill depth of the
Bosphorus and the sea-level curve of Fairbanks
(1989), Aksu et al. (1999) estimated that rising
water levels in the Marmara Sea would have
reached the sill at about 9.5 ka. The rst occurrences of Aubignyna, Porosononion, Nonionella,
Bulimina, Brizalina, Fursenkoina, and Lobatula between 100 and 50 cm in the core (dated radiometrically at 9070 yr BP at a depth of 60 cm) are
entirely consistent with this estimate. Modern assemblages with common Aubignyna and Porosononion are found in water depths of 10^25 m on
the Black Sea shelf, where salinities vary from 11
to 16x (Yanko, 1990). The genera Bulimina and
Brizalina are currently extremely rare within the
modern Black Sea (Yanko and Troitskaja, 1987).
177
Their appearance toward the top of the distal v1

succession at 60 cm is here interpreted as reecting the appearance of more saline waters of Mediterranean origin and the initial establishment of a
salt wedge at this site. Between V9.1 and 6.1 ka,
Black Sea outow had decreased to the point that
planktonic foraminifera were no longer excluded
from the delta, and the appearance of a dysoxic
benthic foraminiferal assemblage reects deposition of the marine drape beneath a stably stratied water column.
Our data suggest a reduction of fresh-water
outow from the Black Sea at V9.1 ka, when
planktonic foraminifera were rst able to live in
surface waters over the distal fringe of the
drowned Holocene delta south of the Bosphorus
exit. This reduction in outow would be a prerequisite for establishment of a two-way ow
through the Bosphorus. Even occasional incursions of Mediterranean water through the strait,
potentially long before a permanent and stable
two-way ow was established, could have allowed
pioneering bottom dwellers like benthic foraminifera to colonise the Black Sea shelf, particularly
those species that tolerate hyposaline conditions.
Infrequent and irregular marine incursions into
marginal seas with restricted entrances are common even today; for example, there are some
years when marine incursions into the modern
Baltic Sea do not occur.
Plate IV.
1a.
1b.
2a.
2b.
3a.
3b.
4.
5.
6.
7.
8.
9.
10.
11.
12a.
12b.
Lobatula lobatula (Walker and Jacob, 1798)

Planorbulina mediterranensis dOrbigny, 1826
Haynesina depressula (Walker and Jacob, 1798)
Nonionella opima Cushman, 1947
Nonionella opima Cushman, 1947
Aubignyna perlucida (Heron-Allen and Earland, 1913)
Gyroidinoides lamarckiana (dOrbigny, 1839)
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MAR97-11
MARGO 3162 4-10-02
^
^
^
^
^
^
^
^
^
^
^
^
^
^
^
^
70
70
70
70
60
60
80
80
40
40
80
80
80
10
10
10
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
cm
Umbilical view U135

Spiral view U135
Spiral view U220
Umbilical view U220
Unattached side U90
Attached side U90
Side view U90
Side view U70
Side view U150
Side view U200
Umbilical view U150
Edge view U150
Edge view U95
Spiral side U100
Spiral side U100
Umbilical view U100
178
Plate V.
MARGO 3162 4-10-02
Evidence for the rst post-glacial colonisation

of the Black by benthic foraminifera was reported
by Yanko and Troitskaja (1987, p. 88) who documented the rst appearance of Holocene foraminifera in a sediment core from the Russian (eastern) Black Sea shelf. These authors reported an
assemblage consisting of Mayerella, Ammonia and
Elphidium in a transgressive interval near the base
of the core, which was dated radiometrically at
9.58 ka. Yanko (1990) indicated that other cores
in the area have yielded similar radiometric dates.
Based on studies of modern foraminiferal distributions in the Black Sea, this assemblage indicates
water depths of 2^3 m and salinities of V4^5x
(Yanko and Troitskaja, 1987; Yanko, 1990).
Yanko (1990) emphasised that the foraminifera
found in this core are of Mediterranean origin.
Clearly, the suggestion by Ryan et al. (1997)
that there was no connection between the Mediterranean and Black Seas until 7.15 ka cannot be
sustained. This is in line with independent evidence from a number of studies that the Black
Sea was persistently exporting brackish water to
the Marmara and Aegean seas from V10.6 ka to
the present (Aksu et al., 1995, 1999, 2002a; Hiscott and Aksu, 2002; CMagatay et al., 2000; Algan
et al., 2001). As argued by Aksu et al. (1999), the
delay, until 7.15 ka, of the arrival of Mediterranean molluscs on the northern shelves of the
Black Sea (Ryan et al., 1997) may be explained
by a protracted replacement of the bottom water
of the Black Sea by saline Mediterranean water so
179
that surface waters remained relatively fresh long

after the establishment of two-way ow.
5.3. The establishment of the stable density
stratication of the Marmara Sea
Benthic foraminiferal data from Cores 97-11,
98-7, and 98-9 were analysed to calculate the
BFOI of Kaiho (1991, 1994) (Fig. 5). Dissolved
oxygen data collected from the Sea of Marmara
show that modern values beneath the halocline
range from between V2 in the western basin
and 0.5 ml/l in the east (Alavi, 1988), which is
well within the useful range of Kaihos BFOI.
At each locality except at the shallowest station
(MAR98-9), the onset of suboxic to dysoxic conditions below the surface mixed later in the Marmara Sea was very rapid. The initial recolonising
assemblages, consisting of Fursenkoina and Cassidulina, are regarded as dysoxic forms in the morphogroup classication of Kaiho (1994). The initial inux of Mediterranean waters into the
Marmara Lake at V12 ka must have quickly
created a stable halocline as the dense marine
water mass displaced the pre-existing, likely
brackish deep water. Although the surface waters
of the Mediterranean were well-oxygenated at the
time, the deeper marine waters of the Marmara
Sea must have been rapidly depleted of oxygen
owing to the oxidation of organic matter and
lack of ventilation of the deep water across the
halocline. Our analysis of the foraminiferal mor-
Plate V.
1.
2.
3.
4.
5a.
5b.
6.
7.
8.
9a.
9b.
10a.
10b.
11.
12.
Discorbinella bertheloti (dOrbigny, 1839)

Ammonia parasovica Stshedrina and Mayer
Ammonia parasovica (Stschedrina and Mayer, 1975)
Ammonia sp. 1 (Cimerman and Langer, 1991)
Ammonia tepida (Cushman, 1926)
Ammonia compacta (Hofker, 1969)
Porosononion martkobi (Bogdanowicz)
Porosononion martkobi (Bogdanowicz)
Elphidium articulatum (dOrbigny, 1839)
Elphidium articulatum (dOrbigny, 1839)
Elphidium macellum (Fitchel and Moll, 1798)
Elphidium translucens Natland, 1938
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
Core
MAR97-11 ^ 70 cm
MAR97-11 ^ 70 cm
MAR98-9 ^ ?? cm
MAR97-11 ^ 150 cm
MAR98-9 ^ 80 cm
MAR98-9 ^ 80 cm
MAR97-11 ^ 150 cm
MAR98-9 ^ ?? cm
MAR98-9 ^ ?? cm
MAR97-11 ^ 110 cm
MAR97-11 ^ 110 cm
MAR97-11 ^ 80 cm
MAR97-11 ^ 80 cm
MAR97-11 ^ 80 cm
MAR98-7 ^ 120 cm
MARGO 3162 4-10-02
Spiral view U125

Umbilical view U125
Umbilical view U75
Spiral view U100
Umbilical view U75
Spiral view U75
Umbilical view U70
Umbilical view U105
Spiral view U100
Side view U160
Apertural view U160
Side view U90
Apertural view U90
Side view U70
Side view U150
180
Fig. 2. Downcore plots of percentage abundances of benthic foraminifera for Core MAR98-9. Radiocarbon dates are fully explained and tabulated in Aksu et al. (2002a).
phogroups and the BFOI (Fig. 5, also summarised in Aksu et al., 2002a) indicates that dissolved oxygen values were even lower during the
initial recolonisation stage than todays values.
The initiation of a strong outow of fresh water
from the Black Sea at V10.5^10.0 ka intensied
the stratication of the Marmara Sea (Fig. 6,
10.0 ka). This outow is linked to the deposition
of sapropel sediments in both the Marmara Sea
(M1) and the Aegean Sea (S1) (Aksu et al., 1995,

2002a; CMagatay et al., 2000). The sparse Chilostomella assemblages and intervals barren of benthic
foraminifera at our deep site (MAR98-12) suggest
the bottom waters of the deep basins may have
been anoxic at times. However, at shelf depths the
oxygen content, although low, was sucient to
sustain communities of predominantly dysoxic
and suboxic benthic foraminifera. CMagatay et
MARGO 3162 4-10-02
181
al. (2000) also report moderate to high benthic

foraminiferal abundances in Holocene sapropel
deposits on the shelves of the Marmara Sea, consistent with higher oxygen contents outside the
deep basinal areas.
After the observed reduction in Black Sea outow occurred at V6.5 ka, oxygenation of the
deep waters in the Marmara Sea improved some-
what. The upper 30^40 cm of the marine drape in

studied cores contain greater proportions of the
oxic foraminiferal morphogroup, which includes
forms such as Discorbinella, Cibicides, Planorbulina, and miliolids. Nevertheless, our data and
those of Yanko et al. (1999) indicate persistent
stratication and predominantly dysoxic taxa.
Signicantly, we did not observe any return to
MARGO 3162 4-10-02
182
fully oxygenated conditions at any time since the

the onset of marine deposition after the last deglaciation.
If the hypothesis of Ryan et al. (1997) is correct, and surface water of Mediterranean origin
had catastrophically inlled the Black Sea at
V7.15 ka, the Marmara Sea would have been
eectively ushed with well-oxygenated Mediterranean waters. The outow from the small rivers
that empty into the southern Marmara Sea shelf
would have been inadequate to create a low-salinity lid over the Marmara Sea. In eect, the Marmara Sea would have become simply an arm of
the Aegean Sea. Had this occurred, typical Med-
MARGO 3162 4-10-02
183
Fig. 5. Calculated BFOI values in the studied cores.
iterranean planktonic and benthic foraminifera

would have been swept into the Marmara Sea
together with the inrushing current, and benthic
foraminiferal faunas would be dominated by the
oxic morphogroup. Our ndings do not support
such a scenario. CMagatay et al. (2000) have made
very similar observations that refute the notion of
catastrophic ooding across the Marmara Sea.
Instead, the exclusive occurrence of dysoxic assemblages throughout the period V10.8^6 ka
supports the scenario of Aksu et al. (1995, 1999,
2002a) that attributes the deposition of sapropels
to stable stratication caused by outow of brackish water from the Black Sea. This brackish outow makes its way into the Aegean Sea via the
Marmara Sea and the intervening straits. Fig. 6
summarises our reconstruction of the history of
water exchange through the Marmara Sea and
connecting straits since 18 ka, and diers only
in detail from the model published by Aksu et
al. (1999, their g. 19).
6. Conclusions
The benthic foraminiferal data from Marmara
Sea cores MAR97-11, MAR98-7, MAR98-9, and
MAR98-12 presented in this study yield the following interpretations:
(1) The Marmara Sea was a brackish, well-oxygenated, inland lake during the last glacial maximum until the Aegean Sea rose to the height of
the Dardanelles sill at V12 ka (Fig. 6). At this
time, molluscs adapted to brackish environments
and only very sparse foraminifera inhabited the
Marmara Sea.
(2) At V12 ka, marine surface waters from the
Aegean Sea were introduced into the deeper parts
of the Marmara Sea basin but left the shelf margins brackish, and initiated a two-way water exchange between the Marmara Sea and the Aegean
Sea through the Dardanelles Strait. The deeper
parts of the Marmara Sea basin show an initial
colonisation of the substrate by abundant pio-
MARGO 3162 4-10-02
184
Fig. 6. Palaeoceanographic reconstruction of water exchange across the Marmara Sea since the last glacial maximum. Horizontal
arrows indicate directions of predominant water ow. Vertical arrows indicate changing water levels.
neering foraminifera, such as Cassidulina, Nonionella, and Fursenkoina; whereas the Marmara
shelf south of the Bosphorus Strait is dominated
by a low-diversity Ammonia assemblage at this
time, indicating brackish conditions. The Dardanelles acted as a faunal lter between the Marmara Sea and the Mediterranean, so that only
shallow-dwelling species have crossed the strait.
(3) After V10.5 ka, there was a decline of the
pioneering foraminifera on the southern Marmara Sea shelf and a subsequent increase in dysoxic forms such as Bulimina and Brizalina. Very
sparse foraminiferal assemblages dominated by
Fursenkoina indicated that anoxia/dysoxia prevailed from V10.6 ka in the deeper parts of the
the basin during the deposition of sapropel M1
(Core MAR98-12). The stable stratication of
the water column prevented mixing, so that dis-
MARGO 3162 4-10-02
solved oxygen contents remained low (below

V1.5 ml/l) beneath the halocline (Fig. 5).
(4) The drowning of the Bosphorus Strait-exit
delta (v1) and the establishment of a salt wedge
over the drowned delta occurred at V9.1 ka. The
benthic foraminifera assemblages reect a continued rise in sea level throughout this period, and
the oxygen content of bottom waters reached a
minimum at this time. Continued sea-level rise
and the reduction in Black Sea outow led to
the establishment of a permanent two-way ow
between the Marmara Sea and the Black Sea
(across the Bosphorus) after V9.1 ka.
(5) The rst appearance and subsequent proliferation of planktonic foraminifera in the shallow
waters near the Bosphorus strait-exit delta at
V6.1 ka indicate the encroachment of more saline surface waters as outow from the Black Sea
diminished. In the upper part of the Holocene
mud drape at all studied localities (after V4.5 ka
in Core MAR98-9), there was an increase in
benthic foraminiferal oxic morphotypes. This suggests a continued reduction in Black Sea outow
and weakening of the halocline.
(6) The benthic foraminiferal data support the
hypothesis of Aksu et al. (1999, 2002a) that Mediterranean Sea water began to ow into the Marmara Sea at V12 ka. At V9.5 ka, rising sea level
reached the Bosphorus sill depth but was unable
to penetrate the Black Sea to a major extent owing to the strong outow of Black Sea surface
water. Foraminiferal assemblages on the Russian
Black Sea shelf (Yanko and Troitskaja, 1987) indicate that some faunal exchange took place as
early as 9.58 ka. By V9.1 ka, brackish water
discharge through the Black Sea^Marmara Sea
gateway decreased suciently to allow the initiation of a stable and persistent two-way ow in the
Bosphorus Strait. Importantly, the hypothesis of
Ryan et al. (1997) that a catastrophic inow of
Mediterranean water penetrated the Black Sea at
V7.15 ka, ooding the arable shelves of the Black
Sea, is incompatible with our observations.
Acknowledgements
We thank Prof. Dr Erol Izdar, the Director of
185
the Piri Reis Foundation for Maritime and Marine Resources Development and Education, and
Prof. Dr Orhan Uslu, the Director of the Institute
of Marine Sciences and Technology, for their support and encouragement. We extend our special
thanks to the ocers and crew of the RV Koca
Piri Reis for their assistance in data acquisition.
We gratefully acknowledge the assistance of Michelle Miskell and Helen Gillespie in core handling and sample preparation. This study was
supported by research and ship-time funds from
the Natural Sciences and Engineering Research
Council of Canada (NSERC) to A.A. and
R.N.H., travel funds from the Dean of Science
at Memorial University of Newfoundland, and
special grants from the Piri Reis Foundation for
Maritime and Marine Resources Development
and Education, Turkey. Foraminiferal analyses
were supported by the KLFR. We are grateful
to Valentina Yanko (Avalon Institute) for checking some of our species identications, and to
Rodolfo Coccioni (University of Urbino) and
Chris Smart (University of Plymouth) for reviewing a draft of the manuscript.
Appendix 1. Taxonomy
The taxonomy of benthic foraminifera reported
here is based primarily on studies of Mediterranean foraminifera of Parker (1958), Jorissen
(1988), Cimerman and Langer (1991), and Sgarrella and Moncharmont Zei (1993) ; the monograph of Black Sea foraminifera by Yanko and
Troitskaja (1987) ; and the study of Marmara
Sea foraminifera by MericM et al. (1995). We also
consulted J.A. Cushmans (1918^1931) eight-part
treatise Foraminifera of the Atlantic Ocean, Saidovas (1975) three-part benthic foraminifera of
the Pacic Ocean, the taxonomical monograph of
Red Sea foraminifera by Hottinger et al. (1993),
Indo-Pacic foraminifera by Loeblich and Tappan (1994), the revision of the HMS Challenger
Foraminifera by Jones (1994), and the monograph of New Zealand foraminifera by Hayward
et al. (1999). Generic classication follows Loeblich and Tappan (1987). Direct comparisons
were made using the M. Al Salameen collection
MARGO 3162 4-10-02
186
of Mediterranean Sea foraminifera housed in the

micropalaeontological collections at UCL.
Adelosina cliarensis (Heron-Allen and Earland,
1930) Plate I, 12, 13
1930 Quinqueloculina cliarensis Heron Allen
and Earland, p. 58, pl. 3, gs. 26, 31.
1991 Adelosina cliarensis (Heron-Allen and Earland) ^ Cimerman and Langer, p. 26, pl. 18, gs.
1^4.
Adelosina dubia (dOrbigny, 1826)
1826 Triloculina dubia dOrbigny, p. 300, no.
24.
1923 Adelosina dubia (dOrbigny) ^ Wiesner, p.
77, pl. 14, g. 193.
1991 Adelosina dubia (dOrbigny) ^ Cimerman
and Langer, p. 27, pl. 18, gs. 5^7.
Adelosina sp. Plate I, 14
Agglutinella arenata (Said, 1949)
1949 Quinqueloculina anguina Said, p. 9, pl. 1,
g. 25.
1988 Quinquelloculina arenata (Said) ^ Haig, p.
233, pl. 4, gs. 15^17.
1994 Agglutinella arenata (Said) ^ Loeblich and
Tappan, p. 306, 307, and 311, pl. 69, gs. 9^11, pl.
70, gs. 10^15, and pl. 74, gs. 10^13.
Ammonia ammoniformis (dOrbigny, 1826)
1826 Rotalia ammoniformis dOrbigny, p. 174,
pl. 12, g. 149.
1974 Ammonia ammoniformis (dOrbigny) ^ Colom, p. 140, g. 23.
1987 Ammonia ammoniformis (dOrbigny) ^
Yanko and Troitskaja, p. 42, pl. 10, gs. 1^10.
Occurrence: Reported from the Mediterranean
and the Atlantic coast of Spain (Colom, 1974)
and from 5 to 220 m depth on the Black Sea Shelf
where it is often very abundant (Yanko and Troitskaja, 1987).
Ammonia beccarii (Linne, 1758)
1758 Nautilus beccarii Linne, p. 710 (de Ellis
and Messina, 1940).
1987 Ammonia beccarii (Linne) ^ Loeblich and
Tappan, p. 664, pl. 767, gs. 1^7.
Ammonia compacta (Hofker, 1964) Plate V, 8

1964 Streblus compactus Hofker, p. 99, gs.
242, 243.
1987 Ammonia compacta (Hofker) ^ Yanko and
Troitskaja, p. 44, pl. 11, gs. 1^10.
Ammonia inata (Seguenza, 1862)
1862 Rosalina inata Seguenza, p. 106, pl. 1,
g. 6.
1988 Ammonia beccarii forma inata ^ Jorissen,
p. 52, pl. 6, gs. 1^4.
1991 Ammonia parkinsoniana (Sequenze) ^ Cimerman and Langer, p. 76, pl. 87, gs. 5, 6.
Ammonia novoeuxinica Yanko, 1979
1979 Ammonia novoeuxinica Yanko, 1979, pl.
24b, g. 1
1987 Ammonia novoeuxinica Yanko ^ Yanko
and Troitskaja, p. 46, pl. 12, gs. 1^3.
Occurrence : Originally described from the
Black Sea Shelf where it was found at depths of
7^56 m (Yanko and Troitskaja, 1987).
Ammonia parasovica Stschedrina and Mayer,
1975 Plate V, 3, 4
1975 Ammonia parasovica Stschedrina and
Mayer, p. 255, pl. 2, gs. 4^6.
1987 Ammonia parasovica Stschedrina and
Mayer ^ Yanko and Troitskaja, p. 47, pl. 12,
gs. 4^6.
1995 Ammonia parasovica ^ MericM et al., pl. 12,
gs. 4a^c.
Occurrence : Originally described from the
Black Sea Shelf where it was found at depths of
5^40 m (Yanko and Troitskaja, 1987); MericM
et al. (1995) rst reported it from the Marmara
Sea.
Ammonia parkinsoniana (dOrbigny, 1839)
1839 Rosalina parkinsoniana dOrbigny, p. 99,
pl. 4, gs. 25^27.
1991 Ammonia parkinsoniana (dOrbigny) ^ Cimerman and Langer, p. 76, pl. 87, gs. 7^9.
1993 Ammonia parkinsoniana (dOrbigny) ^
Sgarrella and Moncharmont Zei, p. 228, pl. 20,
gs. 3^4.
Ammonia tepida (Cushman, 1926) Plate V, 7
MARGO 3162 4-10-02
1926 Rotalia beccarii (Linne) var. tepida

Cushman, p. 79, pl. 1 (de Ellis and Messina,
1940).
1931 Rotalia beccarii (Linne) var. tepida Cushman ^ Cushman, p. 61, pl. 13, g. 3a^c.
1965 Streblus beccarii (Cushman) ^ Todd, p. 29,
pl. 6, g. 1, pl. 7, g. 2.
1988 Ammonia parkinsoniana (dOrbigny) forma tepida Cushman ^ Jorissen, p. 56, pl. 10,
gs. 1^3.
1991 Ammonia tepida (Cushman) ^ Cimerman
and Langer, p. 76, pl. 87, gs. 10^12.
Plate V, 5a,b, 6
1991 Ammonia sp. 1 ^ Cimerman and Langer,
p. 77, pl. 88, gs. 1^4.
Remarks : Valentina Yanko (personal communication to M.A.K., 2001) regards this to be a
form of Ammonia tepida.
Amphicoryna proxima (Silvestri, 1872) Plate
II, 5
1872 Nodosaria proxima Silvestri, p. 63, pl. IV,
g. 138^147.
1994 Amphicoryna proxima (Silvestri) ^ Jones,
pl. 64, g. 5.
Angulogerina angulosa (Williamson, 1858)
1858 Uvigerina angulosa Williamson, p. 67, pl.
5, gs. 3^4.
1987 Angulogerina angulosa (Williamson) ^
Loeblich and Tappan, p. 525, pl. 574, gs. 5^9.
Anomalinoides globulosus (Chapman and Parr,
1937)
1937 Anomalina globulosa Chapman and Parr,
p. 117, pl. 9, g. 27.
1989 Anomalinoides globulosus (Chapman and
Parr) ^ Inoue, pl. 27, g. 8.
Asterigerinata mamilla (Williamson, 1858)
1858 Rotalina mamilla Williamson, p. 54, pl. 4,
gs. 109^111.
1931 Rotalina mamilla (Williamson) ^ Cushman, p. 23, pl. 5, g. 11.
1958 Discorbis mamilla (Williamson) ^ Le Cavez, Y., p. 182.
187
1991 Asterigerinata mamilla (Williamson) ^ Cimerman and Langer, p. 73, pl. 82, gs. 1^4.
1995 Asterigerinata mamilla (Williamson) ^
MericM et al., pl. 10, gs. 4a^d.
Astrononion stelligerum (dOrbigny, 1839)
1839 Nonionina stelligerum dOrbigny, p. 128,
pl. 3, g. 12.
1930 Nonionina stelligerum (dOrbigny) ^ Cushman, p. 7, pl. 8, g. 8^12, pl. 3, g. 1^3.
1991 Astrononion stelligerum (dOrbigny) ^
Cimerman and Langer, p. 74, pl. 84, gs. 13^
15.
Aubignyna perlucida (Heron-Allen and Earland,
1913) Plate IC, 8^10
1913 Rotalia perlucida Heron-Allen and Earland, p. 139, pl. 13, gs. 7^9.
1987 Aubignyna perlucida (Heron-Allen and
Earland) ^ Yanko and Troitskaja, p. 36, pl. 7,
gs. 6^9; pl. 8, g. 1.
1988 Ammonia perlucida (Heron-Allen and Earland) ^ Jorissen, p. 62, pl. 2, gs. 11^12.
1999 Aubignyna perlucida (Heron-Allen and
Earland) ^ Hayward et al., p. 162, pl. 16, gs.
1^3.
Aubignyna planidorso (Atkinson, 1969)
1969 Buccella planidorso Atkinson, p. 535, pl. 6,
g. 3a^c.
1991 Aubignyna planidorso (Atkinson, 1969) ^
Cimerman and Langer, p. 75, pl. 86, gs. 5^6.
Bigenerina nodosaria dOrbigny, 1826 Plate I, 9
1826 Bigenerina nodosaria, dOrbigny, p. 261,
pl. 2, gs. 9^10.
1974 Bigenerina nodosaria dOrbigny ^ Colom,
p. 87, g. 6a^k.
1987 Bigenerina nodosaria dOrbigny ^ Loeblich
and Tappan, p. 172, pl. 191, gs. 1, 2.
1991 Bigenerina nodosaria dOrbigny ^ Cimerman and Langer, p. 21, pl. 9, gs. 1^6.
Biloculinella globula (Bornemann, 1855) Plate
II, 1
1855 Biloculina globulus Bornemann, p. 349, pl.
19, g. 3a,b.
MARGO 3162 4-10-02
188
1891 Biloculina globulus Bornemann ^ Schlumberger, p. 575, pl. 12, g. 97^100.

1991 Biloculina globulus Bornemann ^ Cimerman and Langer, p. 40, pl. 36, g. 1^2.
1922 Bolivina striatula Cushman, p. 27, pl. 3,

g. 10.
1991 Brizalina striatula (Cushman) ^ Cimerman
Bolivina variabilis (Williamson, 1858)

1858 Textularia variabilis Williamson, p. 76, pl.
6, gs. 7^8.
1988 Bolivina variabilis (Williamson) ^ Alavi,
pl. 2, g. 4.
1991 Bolivina variabilis (Williamson) ^ Cimerman and Langer, p. 59, pl. 61, gs. 7^8.
Brizalina sp. 2 (Cimerman and Langer)

1991 Brizalina sp. 2. Cimerman and Langer, p.
60, pl. 62, g. 1
Brizalina alata (Seguenza, 1862) Plate II, 12

1862 Vulvulina alata Seguenza, p. 115, pl. 2, g.
Bulimina aculeata dOrbigny, 1826 Plate III, 3

1826 Bulimina aculeata dOrbigny, p. 269,
g. 7.
1988 Bulimina aculeata dOrbigny ^ Alavi, pl. 1,
g. 12.
1991 Bulimina aculeata dOrbigny ^ Cimerman
and Langer, p. 61, pl. 63, g. 10^11.
5.
1937 Bolivina alata (Seguenza) ^ Cushman, p.
106, pl. 13, gs. 3^11.
1991 Brizalina alata (Seguenza) ^ Cimerman
and Langer, p. 59, pl. 61, gs. 12^14.
1995 Brizalina alata (Seguenza) ^ MericM et al.,
pl. 6, gs. 8a^c.
Brizalina catanensis (Seguenza, 1862) Plate II,
11
1862 Bolivina catanensis Seguenza, pp. 113, 125,
pl. 2, g. 3.
1993 Bolivina catanensis Seguenza ^ Sgarrella
and Moncharmont Zei, p. 208, pl. 14, gs. 4^5.
Brizalina dilatata (Reuss, 1850) Plate II, 13
1850 Bolivina dilatata Reuss, p. 381, pl. 48, gs.
15a^c.
1988 Bolivina dilatata Reuss ^ Alavi, pl. 2, g. 5.
1991 Brizalina dilatata (Reuss) ^ Cimerman and
Langer, p. 59, pl. 62, g. 2.
Brizalina spathulata (Williamson, 1858) Plate
II, 9
1858 Textularia variabilis var. spathulata Williamson, p. 76, pl. 6, gs. 164, 165.
1988 Brizalina spathulata (Williamson) ^ Alavi,
pl. 1, g. 7; pl. 2, g. 10.
1991 Brizalina spathulata (Williamson) ^ Cimerman and Langer, p. 60, pl. 62, gs. 3^5.
Brizalina striatula (Cushman, 1922) Plate II, 10
Brizalina sp. Plate 2, g. 14

Remarks : A airing form with an inated proloculum and a slightly dentate periphery.
Bulimina costata dOrbigny, 1852 Plate III,

5, 6
1859 Bulimina costata dOrbigny, p. 194.
1888 Bulimina alazanensis dOrbigny ^ Alavi,
pl. 1, gs. 6, 8.
1991 Bulimina alazanensis dOrbigny ^ Sgarrella
and Moncharmont Zei, p. 211, pl. 15, g. 3.
Bulimina elongata dOrbigny, 1846 Plate III, 4
1846 Bulimina elongata dOrbigny, p. 187, pl.
11, gs. 19^20.
1991 Bulimina elongata dOrbigny ^ Cimerman
Bulimina inata Seguenza, 1862
1862 Bulimina inata Seguenza, p. 109, pl. 1,
g. 10.
1988 Bulimina inata Seguenza ^ Alavi, pl. 1,
g. 5.
Bulimina marginata dOrbigny, 1875
1875 Bulimina marginata dOrbigny, p. 269, pl.
12, gs. 10^12.
1991 Bulimina marginata dOrbigny ^ Cimerman and Langer, p. 62, pl. 64, gs. 9^11.
1994 Bulimina marginata dOrbigny ^ Jones, p.
55, pl. 51, gs. 3^5.
MARGO 3162 4-10-02
Bulimina sp. Plate III, 7

Remarks : A species with ne, discontinuous
costae.
Canalifera parkerae (Yanko, 1974)
1958 Nonion sp. B ^ Parker, p. 259, pl. 1, gs.
40, 41.
1974 Cribroelphidium parkeri Yanko, p. 24,
pl. 1, g. 1
1987 Canalifera parkerae (Yanko) ^ Yanko and
Occurrence: Reported from the Mediterranean
and Black Sea, where it is found at depths from 7
to 200 m.
Cassidulina crassa dOrbigny, 1839
1839 Cassidulina crassa dOrbigny, p. 56, pl. 7,
gs. 18^20.
1993 Cassidulina crassa dOrbigny ^ Sgarrella
Cassidulina carinata Silvestri, 1896 Plate III, 1, 2
1896 Cassidulina laevigata dOrbigny var. carinata Silvestri, p. 104, pl. 2, g. 10a-c.
1993 Cassidulina carinata Silvestri ^ Sgarrella
Cassidulina laevigata dOrbigny, 1826
1826 Cassidulina laevigata dOrbigny, p. 282.
1987 Cassidulina laevigata dOrbigny ^ Loeblich
and Tappan, p. 504, pl. 555, gs. 1^8.
Cibicides advenum (dOrbigny, 1839)
1839 Truncatulina advena dOrbigny, p. 87, pl.
6. gs. 3^5.
1977 Cibicides advenum (dOrbigny) ^ Le Calvez, Y., p. 122, gs. 1^5.
1991 Cibicides advenum (dOrbigny) ^ Cimerman and Langer, p. 70, pl. 74, gs. 8^10.
1995 Cibicides advenum (dOrbigny) ^ MericM et
al., pl. 9, gs. 4a^c.
Cibicides refulgens deMontfort, 1808
1808 Cibicides refulgens deMontfort, p. 123,
g. 122 (de Ellis and Messina).
1974 Cibicides refulgens deMontfort ^ Colom,
p. 150, g. 31o^t.
189
1987 Cibicides refulgens deMontfort ^ Loeblich

and Tappan, p. 582, pl. 634, g. 1^3.
1991 Cibicides refulgens deMontfort ^ Cimerman and Langer, p. 70, pl. 75, gs. 5^9.
Cornuspira planorbis Schultze, 1854
1854 Cornuspira planorbis Schultze, p. 40, pl. 2,
g. 21.
1993 Cornuspira planorbis Schultze ^ Hottinger
et al., p. 43, pl. 23, gs. 1^3.
Cycloforina rugosa (dOrbigny, 1826)
1826 Quinqueloculina rugosa dOrbigny, p. 302,
g. 24.
1991 Cycloforina rugosa (dOrbigny, 1826) ^ Cimerman and Langer, p. 33, pl. 28, gs. 3^4.
Discorbia candeiana (dOrbigny, 1839)
1839 Rosalina candeiana dOrbigny, p. 97, pl. 4,
gs. 2^4.
1922 Truncatulina candeiana (dOrbigny) ^
Cushman, p. 47, pl. 6, gs. 7^9.
1959 Discorbis candeiana (dOrbigny) ^ Graham
and Militante, p. 93, pl. 13, g. 22.
1977 Discorbia candeiana (dOrbigny) ^ Sellier
de Civrieux, p. 18, pl. 4, gs. 1^8, pl. 5, gs. 1^8,
pl. 6, gs. 1^8, pl. 14, gs. 6^8.
1839 Rosalina bertheloti dOrbigny, p. 135, pl.
1, gs. 28^30.
1884 Discorbinella bertheloti (dOrbigny) ^
Brady, p. 650, pl. 89, g. 10.
1993 Discorbinella bertheloti (dOrbigny) ^ Hottinger et al., p.1114, pl. 150, gs. 1^4.
1999 Discorbinella bertheloti (dOrbigny) ^ Hayward et al., p. 152, pl. 14, gs. 1^3.
Elphidium aculeatum (dOrbigny, 1846)
1846 Polystomella aculeata dOrbigny, p. 131,
pl. 6, gs. 1^4.
1991 Elphidium aculeatum (dOrbigny) ^ Cimerman and Langer, p. 77, pl. 89, gs. 1^4.
Elphidium cf. E. advenum (Cushman, 1922)
cf. 1922 Polystomella advena Cushman, p. 56,
pl. 9, gs. 11, 12.
1991 Elphidium cf. E. advenum (Cushman) ^
MARGO 3162 4-10-02
190
the Mediterranean Sea.
Elphidium articulatum (dOrbigny, 1839) Plate

V, 10a,b
1839 Polystomella articulata dOrbigny p. 30,
pl. 3, gs. 9^10.
1980 Elphidium articulatum (Boltovskoy et al.) ^
Boltovskoy et al., p. 85, pl. 13, gs. 1^4.
Elphidium translucens Natland, 1938 Plate V, 12

1938 Elphidium translucens Natland, p. 144, pl.
5, gs. 3, 4.
1970 Cribrononion translucens (Natland) ^ v.
Daniels, p. 88, pl. 7, gs. 13a,b.
1976 Elphidium translucens Natland ^ Hansen
and Lykke ^ Andersen, p. 11, pl. 7, gs. 1^11.
1991 Elphidium translucens Natland ^ Cimerman and Langer, p. 79, pl. 92, gs. 7^11.
Elphidium depressulum (Cushman, 1933)

1933 Elphidium advenum Cushman var depressulum ^ Cushman p. 51, pl. 12, gs, 4a, b.
1991 Elphidium depressulum Cushman ^ Cimerman and Langer, p. 78, pl. 90, gs. 7^8.
Elphidium jenseni Cushman, 1924
1924 Elphidium jenseni Cushman, p. 49, pl. 16,
gs. 4, 6.
1933 Elphidium jenseni Cushman ^ Cushman, p.
48, pl. 11, gs. 6, 7.
1939 Elphidium jenseni Cushman ^ Cushman, p.
62, pl. 17, gs. 14, 15.
1991 Elphidium jenseni (Cushman) ^ Cimerman
Elphidium granosum (dOrbigny, 1846)
1846 Nonionina granosa dOrbigny, p. 110, pl.
5, gs. 19^20.
1991 Elphidium granosum (dOrbigny) ^ Sgarrella and Moncharmont Zei, p. 229, pl. 21, gs. 1^
2.
Elphidium macellum (Fichtel and Moll, 1798)
Plate V, 11
1798 Nautilus macellum var. beta Fichtel and
Moll, p. 66, pl. 19, g. h^k.
1991 Elphidium macellum (Fichtel and Moll) ^
Cimerman and Langer, p. 78, pl. 89, g. 9.
Elphidium ponticum Dolgopolskaya and Pauli,
1931
1931 Elphidium advenum var. pontica Dolgopolskaya and Pauli, p. 36, pl. 3, g. 14.
1987 Elphidium ponticum Dolgopolskaya and
Pauli ^ Yanko and Troitskaja, p.56, pl. 16, g.
3; pl. 17, gs. 1^3.
Occurrence: Yanko and Troitskaja reported
this species from the Black Sea Shelf and from
Elphidium sp. 2 (Cimerman and Langer)

1991 Elphidium sp. 2 ^ Cimerman and Langer,
p. 80, pl. 90, g. 9.
Elphidium vitreum Collins, 1974
1974 Elphidium vitreum Collins, p. 43, pl. 3,
g. 35.
Evolutononion shansiense N.W. Wang, 1964
1964 Evolutononion shansiense N.W. Wang, p.
58.
1975 Nonion shansiense (N.W. Wang) ^ P.X.
Wang, p. 27, pl. 2, gs. 1^2.
1981 Evolutononion shansiense (N.W. Wang) ^
N.W. Wang, p.15, pl. 1, gs. 1^15.
Favulina hexagona (Williamson, 1848) Plate II,
8
1848 Entosolenia squamosa (Montague) var.
hexagona Williamson, p. 20, pl. 2, g. 23.
1987 Favulina hexagona (Williamson) ^ Hottinger et al., p. 80, pl. 92, gs. 9^13.
1995 Favulina hexagona (Williamson) ^ MericM
et al., pl. 6, g. 7.
Favulina scalariformis (Williamson, 1848)
1848 Entosolenia squamosa (Montague) var.
scalariformis Williamson, p. 13, pl. 2, gs. 21,
22.
1991 Favulina scalariformis (Williamson, 1848)
^ Cimerman and Langer, p. 55, pl. 58, gs. 5^7.
Fursenkoina acuta (dOrbigny, 1846) Plate III,
11, 12
1846 Polymorphina acuta dOrbigny, p. 234, pl.
13, g. 4^5.
MARGO 3162 4-10-02
1848 Virgulina schreibersiana Czjzek, p. 147, pl.

13, g. 18^21.
1972 Virgulina schreibersiana Czjzek ^ Rosset
Moulinier, p. 184.
1985 Fursenkoina acuta (dOrbigny) ^ Papp and
Schmid, p. 82, pl. 75, gs. 1^6.
1991 Fursenkoina acuta (dOrbigny) ^ Cimerman and Langer, p. 64, pl. 67, gs. 1^2.
Globobulimina anis (dOrbigny, 1839) Plate
III, 8
1839 Bulimina anis dOrbigny, p. 105, pl. 2,
gs. 25^26.
1958 Globobulimina anis (dOrbigny), p. 262,
pl. 2, gs. 24^25.
Globocassidulina subglobosa (Brady, 1881)
1881 Cassidulina subglobosa Brady, p. 60.
1884 Cassidulina subglobosa Brady ^ Brady p.
430, pl. 54, g. 17a^c.
1991 Globocassidulina subglobosa (Brady) ^ Cimerman and Langer, p. 61, pl. 63, gs. 4^6.
Gavelinopsis praegeri (Heron-Allen and Earland,
1913)
1913 Discorbina praegeri Heron-Allen and Earland, p. 122, pl. 10, gs. 8^10 (de Ellis and Messina, 1940).
1987 Gavelinopsis praegeri (Heron-Allen and
Earland) ^ Loeblich and Tappan, p. 560, pl.
608, g. 6^12.
1991 Gavelinopsis praegeri (Heron-Allen and
Earland) ^ Cimerman and Langer, p. 66, pl. 70,
gs. 3^4.
Plate IV, 11, 12a,b
1939 Rotalia larmarckiana dOrbigny, p. 131,
pl. 1, gs. 13^15.
1991 Gyroidinoides lamarckiana (dOrbigny) ^
1995 Gyroidina umbonata (Silvestri) ^ MericM et
al., pl. 12, gs. 1a^b.
Gyroidinoides soldanii (dOrbigny, 1826)
1826 Gyroidina soldanii dOrbigny, p. 278,
g. 5.
1991 Gyroidinoides soldanii (dOrbigny, 1826) ^
191

Haynesina anglica (Murray, 1965)
1965 Protelphidium anglicum Murray, 1965, p.
149, pl. 25, gs. 1^5.
1987 Haynesina anglica (Murray) ^ Yanko and
Plate IV, 4, 5
1798 Nautilus depressula (Walker and Jacob), p.
641, pl. 14, g, 33.
1976 Nonion depressulus (Walker and Jacob) ^
Hansen and Lykke ^ Andersen, p. 21, pl. 19, gs.
3, 6.
1978 Haynesina depressula (Walker and Jacob)
^ Banner and Culver, p. 200, pl. 10, g. 1^8.
1991 Haynesina depressula (Walker and Jacob)
^ Cimerman and Langer, p. 81, pl. 83, gs. 1^4.
Homalohedra sp. Plate II, 7
Hyalinea balthica (Schroeter, 1783) Plate III, 13
1783 Nautilus balticus Schroeter, p. 20, pl. 1,
g. 2.
1958 Hyalinea balthica (Schroeter) ^ Parker, p.
275, pl. 4, g. 39.
1993 Hyalinea balthica (Schroeter) ^ Sgarrella
and Moncharmont Zei, p. 234, pl. 22, g. 12.
1995 Hyalinea balthica (Schroeter) ^ MericM et
al., pl. 9, gs. 2a^b.
Occurrence : Generally found at outer neritic to
middle bathyal depths in the eastern Mediterranean (Parker, 1958), it is occasionally found at
shallow stations (25^39 m) in the Gulf of Naples
(Sgarrella and Moncharmont Zei, 1993).
Laevidentalina leguminiformis (Batsch, 1791)
1791 Nautilus (Orthoceras) leguminiformis
Batsch, pp. 2, 5, pl. 3, g. 8a^b.
1993 Dentalina leguminiformis (Batsch) ^ Sgarrella and Moncharmont Zei, p. 194, pl. 11, g. 10.
Laevidentalina sidebottomi (Cushman, 1933)
1933 Dentalina sidebottomi Cushman, p. 12, pl.
3, g. 4.
1994 Laevidentalina sidebottomi (Cushman) ^
Loeblich and Tappan, p. 350, pl. 113, gs. 13^19.
MARGO 3162 4-10-02
192
Lagena doveyensis Haynes, 1973

1973 Lagena doveyensis Haynes, p. 85, pl. 12,
gs. 7^8.
Lagena striata (dOrbigny, 1839) Plate II, 4
1839 Oolina striata dOrbigny, pl. 5, g. 12.
1991 Lagena striata (dOrbigny) ^ Cimerman
Lagena strumosa Reuss, 1858
1858 Lagena strumosa Ruess, p. 434.
1993 Lagena strumosa Ruess ^ Hottinger et al.,
pl. 90, gs. 18^25.
Lenticulina gibba (dOrbigny, 1826) Plate II, 6
1826 Cristellaria gibba dOrbigny, p. 292, no.
17.
1839 Cristellaria gibba dOrbigny, p. 40, pl. 7,
gs. 20, 21.
1913 Cristellaria gibba dOrbigny ^ Cushman,
p. 105, pl. 25, g. 4.
1974 Robulus gibba (dOrbigny) ^ Colom, p. 96,
g. 11 g.
1977 Lenticulina gibba (dOrbigny) ^ Le Calvez,
Y., p. 25, g. 1.
1991 Lenticulina gibba (dOrbigny) ^ Cimerman
and Langer, p. 51, pl. 53, gs. 7^11.
Linaresia bikiniensis (McCulloch, 1977)
1977 Valvulineria (?) bikiniensis McCulloch, p.
349, pl. 134, gs. 9^11.
1990 Linaresia semicribrata (McCulloch) ^
Ujiie, p. 50, pl. 29, gs. 5^6.
1994 Linaresia bikiniensis (McCulloch) ^ Loeblich and Tappan, p. 605, pl. 363, gs. 1^6.
Plate IV, 1a,b, 2a,b
1798 Nautilus lobatulus Walker and Jacob (in
Kanmacher), p. 642, pl. 14, g. 36 (de Ellis
and Messina, 1940).
1958 Cibicides lobatulus (Walker and Jacob) ^
Le Calvez, Y., p. 188.
1987 Lobatula lobatula (Walker and Jacob) ^
Loeblich and Tappan, p. 583, pl. 637, gs. 10^
13.

MericM et al., pl. 9, gs. 3a^b.
Massilina gualtieriana (dOrbigny, 1839)
1839 Quinqueloculina gualtieriana dOrbigny, p.
186, pl. 11, gs. 1^3.
1991 Massilina gualtieriana (dOrbigny) ^ Cimerman and Langer, p. 35, pl. 29, gs. 6^9.
Mayerella brotzkajae (Mayer) emend Yanko,
1987
1968 Elphidiella(?) brotzkajae Mayer, p. 33, g.
52.
1987 Mayerella brotzkajae (Mayer) emend Yanko ^ Yanko and Troitskaja, p. 60, pl. 22, gs. 1^
3; pl. 23, gs. 1^4; pl. 24, gs. 1, 2.
Occurrence : Yanko and Troitskaja (1987) reported this species from low-salinity waters on
the Black Sea shelf (Danube Delta), the Caspian
Sea, and the Aral Sea.
Melonis barleanum (Williamson, 1858)
1858 Nonionina barleana Williamson, p. 32, pl.
3, gs. 68^69.
1993 Melonis barleanum (Williamson, 1858) ^
gs. 1^2.
Melonis pompilioides (Fichtel and Moll, 1798)
1798 Nautilus pompilioides Fichtel and Moll, p.
31, pl. 2, gs. a^c.
1988 Melonis pompilioides (Fichtel and Moll,
1798) ^ Alavi, pl. 2, gs. 6^9.
1991 Melonis pompilioides (Fichtel and Moll,
1798) ^ Cimerman and Langer, p. 74, pl. 85,
gs. 1^4.
Miliolinella labiosa (dOrbigny, 1839)
1839 Triloculina labiosa dOrbigny, p. 178, pl.
10, gs. 12^14.
1923 Miliolina labiosa (dOrbigny) ^Wiesner, p.
71, pl. 134, g. 172.
1929 Triloculina lobiosa dOrbigny ^ Cushman,
p. 60, pl. 15, g. 3.
1991 Miliolinella labiosa (dOrbigny) ^ Cimerman and Langer, p. 41, pl. 3 8, gs. 1^3
MARGO 3162 4-10-02
Miliolinella subrotunda (Montagu, 1803)

1803 Vermiculum subrotunda Montagu, p. 521
(de Ellis and Messina, 1940).
1923 Miliolinella subrotunda (Walker and Boys)
^ Wiesner, p. 69, pl. 13, gs. 165^169.
1991 Miliolinella subrotunda (Montagu) ^ Cimerman and Langer p. 42, pl. 38, gs. 4^9.
Nonionoides auris (dOrbigny, 1839)
1839 Valvulina auris dOrbigny, p. 47, pl. 2, gs.
15^17.
1933 Nonionella auris (dOrbigny) ^ Cushman,
p. 45, pl. 10, g. 10, pl. 11, g. 10, pl. 11, g. 1.
1975 Nonionoides auris (dOrbigny) ^ Saidova,
p. 248.
Remarks : Saidova (1975) transferred this species to her new genus Nonionoides.
Nonionella opima Cushman, 1947 Plate IV, 6, 7
1947 Nonionella opima Cushman, p. 90, pl. 20,
gs. 1^3.
Nonionella turgida (Williamson, 1858)
1858 Rotalina turgida Williamson, p. 50, pl. 4,
gs. 95^97.
1991 Nonionella turgida (Williamson) ^ Cimerman and Langer, p. 74, pl. 84, gs. 6^8.
Parassurina staphyllearia (Schwager, 1866)
1866 Fissurina staphyllearia Schwager, p. 209,
pl. 5, g. 24
1991 Parassurina staphyllearia (Schwager) ^
g. 12.
Plate IV, 3a,b
1826 Planorbulina mediterranensis dOrbigny, p.
280, no. 2.
1931 Planorbulina mediterranensis dOrbigny ^
Cushman, p. 129, pl. 24, gs. 5^8.
Barker, pl. 92, gs. 1^3.
MericM et al., pl. 10, gs. 5a^b
193
Polymorphina sp. A
Porosononion martkobi (Bogdanowicz, 1947)
Plate V, 9a,b
1947 Nonion martkobi Bogdanowicz, p. 30, pl.
4. gs. 4a^c.
1987 Porosononion martcobi (Bogdanowicz)
(sic) ^ Yanko and Troitskaya, p. 52, pl. 18, gs.
1^4.
cf. 1991 Porosononion sp. 1 ^ Cimerman and
Langer, p. 81, pl. 84, gs. 9^12.
Remarks : Found in high numbers within the
deltaic sediments recovered in Core MAR98-9.
On the Black Sea shelf, this species tolerates salinities as low as 11x (Yanko and Trotskaya,
1987). Our identication of this species was veried by Valentina Yanko.
Procerolagena chathamensis (McCulloch, 1977)
1977 Lagena multilatera subsp. chathamensis
McCulloch, p. 41, pl. 50, g. 6.
1994 Procerolagena chathamensis (McCulloch)
^ Loeblich and Tappan, p. 380, pl. 143, gs. 7^11.
Procerolagena implicata (Cushman and McCulloch, 1950)
1950 Lagena implicata Cushman and McCulloch, p. 340, pl. 45, gs. 5^7.
1951 Cushmanina? sp. A. (Cushman and
McCulloch) ^ Hatta and Ujiie, p. 168, pl. 23,
gs. 2^3.
1994 Procerolagena implicata (Cushman and
McCulloch) ^ Loeblich and Tappan, p. 380, pl.
143, gs. 12^13.
Protoglobobulimina pupoides (dOrbigny, 1846)
1846 Bulimina pupoides dOrbigny, p. 185, pl.
11, gs. 11, 12.
1991 Protoglobobulimina pupoides (dOrbigny,
1846) ^ Cimerman and Langer, p. 62, pl. 65,
gs. 1^3.
Pseudononion granuloumbilicatum (Zheng, 1979)
1979 Pseudononion granuloumbilicatum Zheng,
p. 189, 229, pl. 25, g. 6.
MARGO 3162 4-10-02
194
Pygmaeoseistrom islandicum (W.R. Jones, 1984)

1984 Pygmaeoseistrom islandicum W.R. Jones,
p. 134, pl. 7, g. 18.
Pyramidulina catesby (dOrbigny, 1839)
1839 Nodosaria catesbyi dOrbigny, p. 16, pl. 1,
gs. 8^10.
1977 Lagenonodosaria catesbyi (dOrbigny) ^ Le
Calvez, p. 47, gs. 1^5, 8^10.
1994 Pyramidulina catesbyi (dOrbigny) ^ Loeblich and Tappan, p. 353, pl. 116, gs. 10^12.
Plate II, 2a,b
1839 Quinqueloculina patagonica dOrbigny, v.
5, pt. 5, p. 84, pl. 4, gs. 14^16.
Quinqueloculina seminula (Linne, 1758)
1758 Serpula seminulum Linne, p. 786, pl. 2, g.
1a^c.
1991 Quinqueloculina seminula (Linne) ^ Cimerman and Langer, p. 38, pl. 34, gs. 9^12.
Quinqueloculina stalkeri Loeblich and Tappan,
1953
1953 Quinqueloculina stalkeri Loeblich and
Tappan, p. 40, pl. 5, gs. 5^9
1993 Quinqueloculina stalkeri Loeblich and
Tappan ^ Sgarrella and Moncharmont Zei, p.
174, pl. 5, gs. 13^14.
Quinqueloculina stelligera Schlumberger, 1893
Plate II, 3
1893 Quinqueloculina stelligera Schlumberger,
p. 210, textg. 17, pl. 2, gs. 58, 59.
1991 Quinqueloculina stelligera Schlumberger ^
Rectuvigerina phlegeri Le Calvez, 1959 Plate
III, 9
1959 Rectuvigerina phlegeri Le Calvez ^ Berthois and LeCalvez, p. 363, pl. 1, g. 11.
1960 Rectuvigerina raricosta Moncharmont Zei,
pp. 149^150, pl. 4, gs. 18^20.
1988 Rectuvigerina phlegeri Le Calvez ^ Alavi,
pl. 1, g. 4.
1993 Rectuvigerina phlegeri Le Calvez ^

gs. 3, 4.
1995 Rectuvigerina cf. elongastriata (Colom) ^
MericM et al., pl. 7, g. 3.
Rosalina bradyi (Cushman, 1915)
1884 Discorbina globularis ^ Brady (not dOrbigny), p. 178, pl. 86, gs. 8a^c.
1915 Discorbina globularis (dOrbigny) var. bradyi Cushman, p. 12.
1951 Discopulvinulina bradyi (Cushman) ^
Hofker, p. 452, g. 310a,b.
1991 Rosalina bradyi (Cushman) ^ Cimerman
Rosalina catesbyana dOrbigny, 1839
1839 Rosalina catesbyana dOrbigny, p. 99, pl.
4, gs. 22, 24.
1987 Rosalina catesbyana dOrbigny ^ Yanko
and Troitskaja, p. 37, pl. 8, gs. 2^6.
Occurrence : Yanko and Troitskaja (1987) reported this species in water depths less than 25 m
on the Black Sea shelf o the Ukraine. Also
known from the Caspian Sea (Yanko and Troitskaja (1987)).
Rotorbinella lepida McCulloch, 1977
1977 Rotorbinella lepida McCulloch, p. 360, pl.
116, g. 4.
Sigmoilinita sp. 1 (Cimerman and Langer)
1991 Sigmoilinita sp. 1 ^ Cimerman and
Langer, p. 48, pl. 46, gs. 1^5.
Sigmoilina sp. 2 (Cimerman and Langer)
1991 Sigmoilinita sp. 2 ^ Cimerman and
Langer, p. 48, pl. 46, gs. 6^8.
Sigmoilinita tenuis (Czjzek, 1848)
1848 Quinqueloculina tenuis Czjzek, p. 149, pl.
13, gs. 31^34.
1987 Sigmoilinita tenuis (Czjzek) ^ Loeblich and
Tappan, p. 348, pl. 356, gs. 17, 18.
1988 Sigmoilina tenuis (Czjzek) ^ Alavi, pl. 1,
g. 1.
Sigmoilopsis schlumbergeri (Silvestri, 1904)
1904 Sigmoilina schlumbergeri Silvestri, p. 267,
MARGO 3162 4-10-02
textgs. 12^14; p. 481, textg. 6; p. 482, textg. 7.

1986 Sigmoilopsis schlumbergeri (Silvestri, 1904)
^ Van Morkhoven et al. p. 57, pl. 18, g. 1a^
c.
Spiroloculina cymbium dOrbigny, 1839
1839 Spiroloculina cymbium dOrbigny, p. 140,
pl. 3, gs. 5, 6.
1991 Spiroloculina cymbium dOrbigny ^ Cimerman and Langer, p. 29, pl. 22, gs. 1^4.
Spiroloculina dilatata dOrbigny, 1846
1846 Spiroloculina dilatata dOrbigny, p. 271,
pl. 16, gs. 16^18.
1991 Spiroloculina dilatata dOrbigny ^ Cimerman and Langer, p. 30, pl. 22, gs. 5^8.
195
1991 Textularia bocki Hoglund ^ Cimerman

and Langer, p. 21, pl. 10, g. 3^6.
Textularia conica dOrbigny, 1839
1839 Textularia conica dOrbigny, p. 143, pl. 1,
gs. 19, 20.
1899 Textularia conica dOrbigny ^ Flint, p.
285, pl. 29, g. 6.
1923 Textularia conica dOrbigny ^ Cushman,
p. 11, pl. 2, gs. 8^10.
1991 Textularia conica dOrbigny ^ Cimerman
Textularia cushmani Said, 1949 Plate I, 5, 6a,b
1949 Textularia cushmani Said, p. 7, pl. 1, g.
13.
1995 Spiroplectinella saggitula (dOrbigny) ^
MericM et al., pl. 1, gs. 2a^b.
Spiroloculina excavata dOrbigny, 1846 Plate I,

11
1846 Spiroloculina excavata dOrbigny, 1846 p.
271, pl. 16, gs. 19^21.
1991 Spiroloculina excavata dOrbigny ^ Cimerman and Langer, p. 30, pl. 23, gs. 1^3.
1995 Spiroloculina excavata dOrbigny ^ MericM
et al., pl. 2, g. 4.
Spiroloculina tenuiseptata Brady, 1884 Plate I, 10
1884 Spiroloculina tenuisepta Brady, p. 153, pl.
10, g. 5.
1991 Spiroloculina tenuisepta Brady ^ Cimerman and Langer, p. 31, pl. 24, gs. 6^9.
1995 Spiroloculina tenuisepta Brady ^ MericM et
al., pl. 2, gs. 5a^b.
Spirorutilus spp. Plate I, 3, 4a,b
1991 Spiroplectinella sagittula (dOrbigny) ^ Cimerman and Langer, p. 20, pl. 6, gs. 5^6.
Remarks : The specimen illustrated by Cimerman and Langer (1991) as Spiroplectinella sagittula is misidentied and rightly belongs in the
genus Spirorutilus. Textularia sagittula is the
type species of Textularia, and cannot be transferred to a dierent genus.
Textularia bocki Hoglund, 1947 Plate I, 1, 2
1947 Textularia bocki Hoglund, p. 171, pl. 12,
gs. 5, 6.
Textularia stricta Cushman, 1911

1911 Textularia stricta Cushman, p. 11, text g.
13.
1951 Valvotextularia stricta (Cushman) ^
Hofker, p. 33, g. 11.
1966 Textulina srticta (Cushman) ^ Norvang, p.
6, pl. 1, g. 1, pl. 2, gs. 1^2.
1994 Textularia stricta (Cushman) ^ Loeblich
and Tappan, p. 275, pl. 38, gs. 1^9.
Textularia truncata Hoglund, 1947
1947 Textularia truncata Hoglund, p. 175, pl.
12, gs. 8, 9, textgs. 147^149.
1991 Textularia truncata Hoglund ^ Cimerman
1995 Textularia truncata Hoglund ^ MericM et
al., pl. 1, gs. 5a-c.
Textularia sp. Plate I, 7, 8a,b
Triloculina tricarinata dOrbigny, 1826
1826 Triloculina tricarinata dOrbigny, p. 299.
1991 Triloculina tricarinata dOrbigny ^ Cimerman and Langer p. 46, pl. 44, gs. 3^4.
Uvigerina bradyana Fornasini, 1900
1900 Uvigerina bradyana Fornasini, p. 390, textg. 40.
MARGO 3162 4-10-02
196
1994 Uvigerina bradyana Fornasini ^ Loeblich

and Tappan, p. 128, pl. 250, gs. 1^6.
1999 Uvigerina bradyana Fornasini ^ Hayward
et al., p. 135, pl. 9, g. 27.
1958 Uvigerina mediterranea Hofker ^ Parker,

p. 263, pl. 2, gs. 39, 40.
1988 Uvigerina mediterranea Hofker ^ Alavi, pl.
2, g. 1.
1991 Uvigerina mediterranea Hofker ^ Cimerman and Langer p. 63, pl. 65, gs. 7^9.
Uvigerina mediterranea Hofker, 1932 Plate III,

10
1932 Uvigerina mediterranea Hofker, p. 118,
textgs. 32a^g.
Vaginulina lequilensis Fornasini, 1901

1901 Vaginulina lequilensis, Fornasini, p. 60, p.
61, text g. 13.
Appendix 2. Benthic foraminiferal data (number of specimens per sample)

Core MAR98^9
Depth in centimetres
?Eponides sp.
?Haynesina sp. Cimerman
?Mayerella spp.
Adelosina spp.
Ammonia beccarii
Ammonia sp. 1
Ammonia tepida
Amphicoryna spp.
Angulogerina spp.
Anomalinoides spp.
Astacolus spp.
Astigerinata mammila
Aubignyna perlucida
Bulimina costata
Bulimina marginata
Bulimina aculeata
Bigenerina nodosaria
Biloculinella spp.
Bolivina spp.
Brizalina spp.
Bulimina elongata
Cassidulina crassa
Cassidulina carinata
Chilostomella spp.
Cibicides refugens
Cibicides sp.
Discorbinella bertheloti
Elphidium cuvielleri
Elphidium spp.
Favulina hexigona
Fissurina neptuna
Fursenkoina acuta
Gavelinopsis praegeri
Globobulimina spp.
Globocassidulina subglobosa
Gyroidinoides lamarckiana
Haynesina depressula
Hyalinea balthica
Laevidentalina spp.
Lagena semistriata
10
20
1
1
30
40
3
3
2
3
2
50
60
70
32
80
90
100
110
120
26
1
51
3
49
11
5
1
2
108
17
8
113
5
2
6
14
4
7
19
1
2
97
16
21
26
2
2
2
81
28
1
30
4
1
2
2
1
1
4
5
11
5
3
2
6
14
1
5
13
12
1
4
15
13
1
4
17
1
34
1
42
3
5
5
14
12
1
8
14
4
19
2
7
13
48
34
3
20
9
89
26
29
3
1
85
31
1
30
1
2
1
76
60
1
27
3
1
43
48
5
13
26
1
13
1
3
14
6
4
1
1
1
3
6
1
2
1
1
3
2
2
2
5
2
1
1
4
3
2
1
1
2
1
1
MARGO 3162 4-10-02
197
Appendix 2 (Continued).
Core MAR98^9
Depth in centimetres
Lagena sp. (smooth)

Lagena striata
Lenticulina gibba
Lobatula lobatula
Nonion sp.
Nonionella opima
Nonionella turgida
Planorbulina mediterranensis
Porosononion martkobi
Quinqueloculina seminula
Quinqueloculina spp.
Rectuvigerina phlegeri
Rosalina spp.
Sigmoilinita tenuis
Siphotextularia spp.
Spiroloculina excavata
Spiroloculina tenuisepta
Spirorutilus spp.
Textularia spp.
Unident. Trochospiral w
arched limbate sutures
Uvigerina sp.
Valvulina spp.
Total benthic foraminifera
Core MAR98-7
Depth in centimetres:
Agglutinella arenata
Ammonia ammoniformis
Ammonia beccarii
Ammonia compacta
Ammonia inata
Ammonia novoeuxinica
Ammonia pakinsoniana
Ammonia sp. 1 (Cimerman)
Ammonia tepida
Amphicoryna scalaris
Angulogerina angulosa
Anomalinoides globulosus
Asterigerinata cf. mamilla
Astrononion stelligerum
Aubignyna perlucida
Biloculinella globula
Bolivina variabilis
Brizalina alata
Brizalina catanensis
Brizalina dilatata
Brizalina sp. 2 (Cimerman)
Brizalina spathulata
Bulimina aculeata
Bulimina costata
Bulimina elongata
10
20
30
40
50
60
70
80
90
100
110
120
22
10
1
15
18
1
33
47
1
1
10
1
1C s
1
1
2
1
1
1
2
2
1
2
2
3
2
2
2
2
19
14
2
12
5
8
3
18
20
4
1
3
18
11
1
6
248
5
254
2
217
239
2
205
20
30
40
1
1
50
60
1
2
1
6
6
22
10
6
2
1
10
2
8
3
11
22
53
31
15
45
41
30
16
2
242
198
222
191
192
168
252
185
70
80
90 100 110 120 130 140 150 160 170 180
2
1
1
1
1
1
3
2
3
1
1
2
7
2
6
6
1
3
1
3
1
1
3
1
12
1
3
19
1
14
12
46
19
19
25
107
33
7
21
7
7
3
29
37
68 134
26 39
5
6
15 26
5
8
12 13
40 138
25
79 70
21 40
2
5
9 16
1
1
1
1
2
3
1
12
4
24
5
52 40
6
77 51
38 128
1
14 31
3
1
3
12
43
1
3
54
45
2
5
4
1
1
1
1
1
3
1
10
MARGO 3162 4-10-02
198
Core MAR98-7
Bulimina inata
Bulimina marginata
Canalifera parkerae
Cassidulina crassa
Cassidulina laevigata
Cibicides advenum
Cibicides refugens
Cornuspira planorbis
Cycloforina rugosa
Discorbia candeiana
Elphidium aculeatum
Elphidium advenum
Elphidium jenseni
Elphidium macellum
Elphidium ponticum
Elphidium sp. 2 (Cimerman)
Elphidium translucens
Elphidium depressulum
Evolutononion shansiense
Favulina hexagona
Favulina scalariformis
Fursenkoina acuta
Globobulimina anis
Globobulimina globula
Gravelinopsis praegeri
Gyroidinoides soldanii
Haynesina anglica
Hyalinea balthica
Laevidentalina sidebottomi
Lagena doveyensis
Lagena striata
Lenticulina gibba
Lobatula lobatula
Mayerella brotzkajae
Melonis barleanum
Melonis pompilioides
Miliolinella labiosa
Miliolinella subrotunda
Nonionella opima
Nonionella turgida
Polymorphina sp. A
Procerolagena chathamensis
Protobulimina pupoides
Pygmaeoseistrom islandicum
Quinqueloculina patagonica
Quinqueloculina stalkeri
Rectuvigerina phlegeri
10
20
30
40
50
60
70
80
9
38
3
18
9
21
3
38
1
62
3
23 104
43
27
13
30
9
30
14
12
6
9
11
6
10
8
16
38
59
9
2
3
90 100 110 120 130 140 150 160 170 180

2
10
1
1
2
1
1
1
1
1
2
10
10
8
7
14
1
2
3
1
4
7
1
4
1
1
2
2
2
2
6
12
5
1
2
5
1
1
2
2
3
24
1
52
1
1
3
9
1
2
9
21
11
1
1
1
1
18
3
3
2
16
1
1
2
2
1
1
3
3
2
1
5
1
30
32
16
1
1
11
12
3
5
1
24
12
5
18
1
2
9
2
1
7
3
4
13
2
4
MARGO 3162 4-10-02
1
2
1
1
3
199
Core MAR98-7
Rosalina bradyi
Rosalina catesbyana
Sigmoilina sp. 1
Sigmoilina sp. 2 (Cimerman)
Sigmoilina tenuis
Spiroloculina cymbium
Spiroloculina dilatata
Spiroloculina tenuiseptata
Spirorutilus spp.
Textularia bocki
Textularia conica
Textularia striata
Textularia truncata
Triloculina tricarinata
Uvigerina bradyana
Uvigerina mediterranea
Valvulineria bradyana
Valvulineria minuta
Planktonic Foraminifera
Core MAR97-11
Adelosina cliarensis
Adelosina dubia
Ammonia compacta
Ammonia inata
Ammonia parasovica
Ammonia tepida
Amphicoryna scalaris
Angulogerina angulosa
Aubignyna perlucida
Aubignyna planidorso
Biloculinella globula
Brizalina alata
Brizalina catanensis
Brizalina dilatata
Brizalina spathulata
Brizalina striatula
Bulimina aculeata
Bulimina costata
Bulimina elongata
Bulimina inata
Bulimina marginata
Cassidulina crassa
Cibicides advenum
Eilohedra levicula
Elphidium advenum
Elphidium articulatum
Elphidium granosum
10
20
30
40
50
60
70
80
90 100 110 120 130 140 150 160 170 180

1
2
4
2
2
2
11
11
8
3
4
1
8
1
1
3
3
2
1
1
20
6
17
13
1
1
1
1
1
5
6
7
2
5
8
8
10
1
4
12
9
7
1
1
5
6
3
2
8
1
4
5
2
3
18
2
21
2
3
1
1
1
6
4
2
2
2
136 69 222 38 47 66 68 15
549 344 501 296 491 332 501 414
10
20
30
40
50
32
60
70
80
10
89
90
3
39
5
39
100
110
20
16
120
130
140
150
2
1
1
1
1
1
2
3
2
19
43
33
100
1
24
24
40
38
234
10
13
143
7
11
50
3
33
12
151
16
45
43
26
105
382
1
82
4
47
22
276
8
60
16
29
1
7
17
11
8
5
19
52
2
3
1
3
11
128
43
141
26
43
39
70
15
14
19
17
83
4
19
5
159
5
7
1
44
148
1
17
2
276
18
40
33
38
197
28
39
11
1
2
2
4
1
4
93
33
78
27
17
18
34
170
2
410
52
1
2
1
1
1
2
MARGO 3162 4-10-02
4
2
200
Core MAR97-11
Elphidium macellum
Elphidium sp.
Elphidium vitreum
Favulina hexagona
1
Fursenkoina acuta
1
2
3
Gyroidinoides soldanii
Hanzawaia sp.
Homalohedra sp.
Hyalinea balthica
44
Laevidentalina leguminiformis
1
Lagena striata
Lagena strumosa
Lenticula gibba
Linaresia bikiniensis
Lobatula lobatula
Massilina gualtieriana
3
Melonis barleanum
Melonis pompilioides
Miliolinella subrotunda
7
Nonionella auris
Nonionella opima
Nonionella turgida
Parassurina staphyllearia
Polymorphina sp. A
Procerolagena implicata
Pseudononion granuloumbilicatum
Pulleniatina obliquiloculata
Pyramidulina catesby
Quinqueloculina patagonica
Quinqueloculina seminula
Quinqueloculina stelligera
Rotorbinella lepida
Sigmoilina tenuis
8
Sigmoilopsis schlumbergeri
Spiroloculina cymbium
1
Spiroloculina dilatata
1
Spiroloculina tenuiseptata
4
Spirorutilus sp.
9
Textularia bocki
28
Textularia conica
23
Textularia cushmani
Textularia cf. truncata
3
Uvigerina bradyana
3
Uvigerina mediterranea
Vaginulina lequilensis
Planktonic foraminifera
134
560
10
20
30
40
50
60
70
80
90
1
1
1
1
30
1
206
2
1
2
1
34
100
110
120
130
140
150
1
2
1
6
20
6
7
14
3
20
1
33
1
32
1
2
2
1
1
1
1
37
24
3
1
2
1
2
4
1
22
21
10
17
28
6
8
5
2
4
3
16
1
1
10
11
1
1
3
2
1
11
4
1
17
4
1
1
10
1
2
1
6
22
24
1
2
6
12
1
4
1
2
1
7
14
36
3
6
1
428
860
430
1234
6
1
1
10
8
2
2
24
8
4
4
13
8
8
1
8
4
3
10
1
6
1
1
1
1
34
509
59
846
1
350
330
600
MARGO 3162 4-10-02
819
4
137
1
12
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Marine Geology 190 (2002) 165^202

Late Glacial to Holocene benthic foraminifera in the

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

Black Sea following the last deglaciation. On the

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

benthic foraminifera within the Marmara Sea itself.

Zeiss-940 digital scanning electron microscope at

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

Kaihos (1991, 1994) BFOI is an empirical ratio

anities to those described from the modern

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

silt and clay, and reects increasing water depths

At 70 cm in the core, an abrupt change in the

Textularia bocki Hoglund, 1947

Side view U90

Side view U180

Side view U100

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

Dreissena rostriformis distincta is present. Benthic

elevation coincides with the modern depth of the

Biloculinella globula (Bornemann, 1855)

MARGO 3162 4-10-02

Oblique side view U500

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

depths in the eastern Mediterranean. Rare (and

Cassidulina carinata Silvestri, 1896

MARGO 3162 4-10-02

Side view U155

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

the southern entrance of the Bosphorus, and by

Their appearance toward the top of the distal v1

Lobatula lobatula (Walker and Jacob, 1798)

MARGO 3162 4-10-02

Umbilical view U135

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

MARGO 3162 4-10-02

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

Evidence for the rst post-glacial colonisation

that surface waters remained relatively fresh long

Discorbinella bertheloti (dOrbigny, 1839)

MARGO 3162 4-10-02

Spiral view U125

M.A. Kaminski et al. / Marine Geology 190 (2002) 165^202

(M1) and the Aegean Sea (S1) (Aksu et al., 1995,