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363
Short Communication
DIATOM BIOSTRATIGRAPHY
EASTERN JAVA (INDONESIA)
OF
LATE
MIOCENE
AND
PLIOCENE
SEDIMENTS
OF
LLOYD H. BURCKLE
Lamont-Doherty Geological Observatory, Palisades, New York 10964 (U.S.A.)
Abstract
Burckle, L.H., 1982. Diatom biostratigraphy of Late Miocene and Pliocene sediments of eastern Java (Indonesia).
Mar. Micropaleontol., 7 : 363--368.
A study of the marine diatoms of the Late Miocene to Pliocene Njepung section (Java) yield results that are
in substantial agreement with Saint-Marc and Suminta (1979). The lower part of the Globigerina Marls belongs
to the Late Miocene/Early Pliocene Thalassiosira convexa zone of Burckle (1972) while the middle of the formation belongs to the Middle Miocene Nitzschia jousea zone of Burckle (1972). An open ocean environment is indicated while the abundant presence of Thalassiosira nitzschioides suggests strong upwelling, at least in the lower
part of the Globigerina Marls.
Introduction
Within t h e past few years, a n u m b e r o f
p a p e r s have b e e n p u b l i s h e d on t h e m i c r o fossil b i o s t r a t i g r a p h y
o f L a t e Miocene/
latest-Pliocene sections in c e n t r a l and e a s t e r n
Java. ( N i n k o v i c h and Burckle, 1 9 7 8 ; SaintMarc and S u m i n t a , 1 9 7 9 ; V a n Gorsel and
T r o e l s t r a , 1981.) In a d d i t i o n t o i d e n t i f y i n g
b i o s t r a t i g r a p h i c m a r k e r s , these p a p e r s have
addressed such p r o b l e m s as p a l e o c l i m a t e ,
paleoceanography, the timing of the emergence o f this p o r t i o n o f J a v a as well as t h e
t i m i n g o f t h e first a p p e a r a n c e o f h o m i n i d s
in J a v a ( N i n k o v i c h and Burckle, 1 9 7 8 ; Nink o v i c h et al., 1 9 8 2 ) . T h e sections studied b y
Saint-Marc and S u m i n t a {1979) and Van
Gorsel and T r o e l s t r a ( 1 9 8 1 ) are l o c a t e d a
s h o r t d i s t a n c e f r o m t h e B o d j o n e g o r o Well
No. 1 (Bolli, 1 9 6 6 ) and serve to c o m p l e m e n t
its f o r a m i n i f e r a l b i o s t r a t i g r a p h y .
T h r o u g h t h e c o u r t e s y o f Saint-Marc, I
o b t a i n e d s a m p l e s ( s o m e 70 in all) f r o m t h e
N j e p u n g section (Saint-Marc and S u m i n t a ,
1 9 7 9 ) in eastern J a v a for d i a t o m analysis.
T h e N j e p u n g section, m o r e t h a n 6 5 0 m
t h i c k , is l o c a t e d 50 k m s o u t h w e s t o f Bodjon e g o r o and consists o f t h e L a t e M i o c e n e
K e r e k l i m e s t o n e overlain b y t h e L a t e Mioc e n e - - P l i o c e n e G l o b i g e r i n a Marls f o r m a t i o n
and t h e Pleistocene N j e p u n g l i m e s t o n e . T h e
results o b t a i n e d b y these t w o a u t h o r s are
s u m m a r i z e d in Fig. 1. A hiatus was identified at t h e c o n t a c t b e t w e e n the K e r e k
F o r m a t i o n and t h e G l o b i g e r i n a Marls w i t h i n
t h e G l o b o r o t a l i a acostaensis Z o n e . T h r e e
additional
foraminiferal zones
gave t h e
a u t h o r s sufficient d a t a to tie t h e i r section
t o t h e B o d j o n e g o r o Well o f Bolli (1966).
T h e regional g e o l o g y o f t h e N j e p u n g area
has b e e n s u m m a r i z e d b y Saint-Marc and
S u m i n t a ( 1 9 7 9 ) . T h e region is within an
364
NJEPUNG
FORMATI
SECT ON
ONS
ZONES
NJEPUNG
LIME
FORAM.
DIATOM
This
ZONES
poper
~roposed
tie to
~aleomac
stratig "
~.GE
G.
truncatulinoides
STONE
Middle
port of
6O
< 59
GAUSS
[LLq
obliquiloculata
.-%
\49
GLOBI
G.
G E RI N A
Mid to
upper
port of
-42
MARLS
- :59
margar/tae
GILBER
/ 50
X 29
,-@
N22
Lower
G.
--15
Th.
p o r t of
con vex a
$1LBER
acostaens/s
-11
EPOCH
5
1 8.----~-~ -
G.
LIME
STONE
acostaensi$
365
east--west trending anticlinorium (the Kendeng Zone). Paralleling it to the south is the
east--west trending volcanic high of Java,
while to the north is the Rembang uplift.
The Kendeng Zone was submerged during
the Late Miocene and Pliocene and was
apparently deep enough for open ocean conditions to prevail. Progressive uplift from the
south eventually led to emergent conditions
in this region during the latest Pliocene.
Methods
Samples were prepared using procedures
described by Burckle et al. (1978}. This is
a modification of a "standard" method
described by Schrader (1974} and is not
much different from that used by most
diatomists. Identification of major index
species follow that of Muchina (1963),
Burckle (1972), and Schrader (1974) while
the ranges of these species are taken from
Burckle (1972, 1977, 1978), Burckle and
Opdyke (1977) and Kazarina (1975). In
these papers, all ranges of all index species
have been tied directly to the paleomagnetic
reversal record. Of the 70 samples examined,
samples 1 to 29 and 39 to 41 contained
diatoms (Fig. 1). The remaining samples
were barren of this group, or the diatoms
were in too poor a state of preservation for
identification.
Biostratigraphy
The late Cenozoic planktonic diatom
zonation of Burckle (1972, 1978) is used in
this study. The Epoch and Age boundaries
follow the usage of Cita (1975), Saito et al.
(1975), Berggren and Van Couvering (1974),
Van Couvering et al. (1976), and Berggren
et al. (1980}, in that the Miocene/Pliocene
boundary is placed just above the Epoch 5/
Gilbert Magnetic Epoch boundary and the
Pliocene/Pleistocene boundary is placed in
the Olduvai Event of the Matuyama Reversed
Magnetic Epoch. In their study, Saint-Marc
and Suminta (1979) followed the usage of
366
yama Reversed Epoch). This form occurs in
samples 8 to 29 and 39 to 41. Finally, I
note the occurrence of Nitzschia jouseae
Burckle in samples 39 to 41. This species
ranges in the Pliocene from the " c " event
of the Gilbert to the upper part of the Gauss
Normal Epoch. The most abundant species
found in most samples is Thalassionema
nitzschioides Grunow and Th. nitzschioides
var. parva. These two forms are quite cosmopolitan, but occur most abundantly in
upwelling areas along eastern boundary currents (Cook-Poferl et al., 1975).
Discussion
367
for this sample, sometime during the Gilbert
Reversal Magnetic Epoch. I use negative
evidence because both of these species are
found in the equatorial Atlantic and IndoPacific (Burckle, 1972; Schrader, 1974;
Kazarina, 1975), and thus, their presence
should be expected in the Njepung section
particularly since Ninkovich and Burckle
(1979) and Ninkovich et al. (1982) report
the presence of these two species in sections
from central Java. The composition of the
diatom
flora
{abundant
Thalassionema
nitzschioides and var. parva and such open
ocean tropical and subtropical forms as
Nitzschia marina, Coscinodiscus nodulifer,
Hernidiscus cuneiforrnis and Coscinodiscus
radiatus Ehrenberg) support the conclusion
of Saint-Marc and Suminta (1979) that
this section represents a largely deep water,
open ocean environment. Abundant Thalassionerna nitzschioides is associated with a
strongly upwelling marine environment usually along an eastern boundary current. In
previous studies (Cook-Poferl et al., 1975, and
author's unpublished notes) an assemblage
dominated by Thalassionerna nitzschioides
in surface sediments was found to be associated with the Peru--Chile current. Burckle
et al. (1982) noted the initiation of the
Th.
nitzschioides
dominated assemblage
occuring at the same time as a major global
cooling. Finally, Schrader (in Berggren et
al., 1976) has pointed out the close association between a Th. nitzschioides dominated
assemblage and coastal upwelling in the E1
Cuervo section of southern Spain.
Conclusions
Diatom results from the Late Miocene/
Pliocene Njepung section of eastern Java
are in substantial agreement with results from
the Foraminifera. They provide additional
ties to the paleomagnetic reversal records.
Correlations are made as follows.
(1) The lower part of the Globigerina
Marls belong to the Thalassiosira convexa
zone of Burckle (1972).
368
in marine and continental sequences. Paleogeogr.,
Palaeoclimatol., Palaeoecol., 16 (1/2): 1--216.
Berggren, W.A., Benson, R.H., Haq, B.U., Riedel,
W.R., Sanfilippo, A., Schrader, H.J. and Tjalsma,
R.C., 1976. The E1 Cuervo section (Andalusia,
Spain): micropaleontologic anatomy o f an early
Late Miocene lower bathyal deposit. Mar. Micropaleontol., 1 : 195--247.
Berggren, W.A., Burckle, L.H., Cita, M.B., Cooke,
H.B.S., Funnell, B.M., Gartner, S., Hays, J.D.,
Kennett, J.P., Opdyke, N.D., Pastouret, L.,
Shackleton, N.J. and Takayanagi, Y., 1980.
Towards a quaternary time scale. Quat. Res., 13:
277--302.
Bolli, H.M., 1966. The planktonic foraminifera in
well Bodjonegoro-1 of Java. Eclogae Geol. Helv.,
59 : 449--465.
Burckle, L.H., 1972. Late Cenozoic planktonic
diatom zones from the eastern equatorial Pacific.
Nova Hedwigia, 39 : 217--246.
Burckle, L.H., 1977. Pliocene and Pleistocene diatom
datum levels from the equatorial Pacific. Quat.
Res., 7 : 330--340.
Burckle, L.H., 1978. Late Miocene to Early Pliocene
high resolution diatom biostratigraphy for the
Central Pacific. Geol. Soc. Am., Abstracts with
Program, 7 : 374.
Burckle, L.H. and Opdyke, N.D., 1977. Late Neogene
diatom correlations in the circum-Pacific. Proc.
Int. Congr. Pacific Neogene Stratigraphy, 1st,
T o k y o , pp. 255--284.
Burckle, L.H., Clarke, D.B. and Shackleton, N.J.,
1978. Isochronous last-abundant-appearance datum (LAAD) o f the diatom Hemidiscus karstenii
in the sub-Antarctic. Geology, 6: 243--246.
Burckle, L.H., Keigwin, L.D. and Opdyke, N.D.,
1982. Middle and Late Miocene stable isotope
stratigraphy: correlation of the Paieomagnetic
Reversal Record. Micropaleontology. In press.
Cita, M.B., 1975. The Miocene--Pliocene boundary:
history and definition. In: T. Saito and L.H.
Burckle (Editors), Late Neogene Epoch Boundaries. Micropaleontology Press, New York, N.Y.,
pp. 1--30.
Cooke-Proferl, K., Burckle, L.H. and Riley, S., 1975.
Diatom evidence bearing on late Pleistocene climatic changes in equatorial Pacific. Annual Mtg.
Geol. Soc. Am., Abstracts with Program, pp.
1038--1039.