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Geological Survey of Denmark and Greenland (GEUS), ster Voldgade 10, DK-1350 Copenhagen K, Denmark
Vietnam Petroleum Institute (VPI), Yen Hoa, Cau Giay, Hanoi, Viet Nam
a r t i c l e i n f o
a b s t r a c t
Article history:
Received 26 September 2007
Received in revised form
26 March 2008
Accepted 16 April 2008
Available online 25 December 2008
The Cuu Long Basin (Mekong Basin) is a rift basin off southern Vietnam, and the most important
petroleum producing basin in the country. However, information on petroleum type and characteristics
has hitherto been largely unavailable to the public. This paper presents petroleum geochemical data on
nine oil samples from four different producing elds in the Cuu Long Basin: the Dragon (Rong), Black Lion
(Sutu-Den), Sunrise (Rang ong) and White Tiger (Bach Ho) Fields. The oils are highly parafnic with
bimodal normal alkane distributions and show moderate pristane to phytane ratios and a conspicuous
hyperbolic decrease in abundance with increasing carbon number of hopane homologues from C30 to C35.
The TPP-index of Holba et al. (Holba, A.G., Dzou, L.I., Wood, G.D., Ellis, L., Adam, P., Schaeffer, P., Albrecht,
P., Greene, T., Hughes, W.B., 2003. Application of tetracyclic polyprenoids as indicators of input from
freshbrackish water environments. Organic Geochemistry 34, 441469) is equal to 1 in all samples
which in combination with tricyclic triperpane T26/T25 ratios >1 and the n-alkane and hopane distributions mentioned above provide a strong indication of an origin from lacustrine source rocks. This is
supported by the absence of marine C30 desmethyl steranes (i.e. 24-n-propylcholestanes) and marine
diatom-derived norcholestanes. Based on the overall biological marker distributions, the lakes probably
belonged to the overlled or balanced-ll types dened by Bohacs et al. (Bohacs, K.M., Carroll, A.R., Neal,
J.E., Mankiewicz, P.J., 2000. Lake-basin type, source potential, and hydrocarbon character. An integrated
sequence-stratigraphicgeochemical framework. AAPG Studies in Geology 46, 334). The oils were
generated from source rocks at early- to mid-oil-window maturity, presumably Oligocene lacustrine
shales that are present in the syn-rift succession. Oils from individual elds may, however, be distinguished by a combination of biological marker parameters, such as the oleanane index, the gammacerane
index, the relative abundance of tricyclic terpanes, the proportions of diasteranes and 28-norspergulane,
complemented by other parameters. The oils of the Cuu Long Basin show an overall similarity to the B-10
oil from the Song Hong Basin off northern Vietnam, but are markedly different from the seepage oils
known from Dam Thi Nai on the coast of central Vietnam.
2008 Elsevier Ltd. All rights reserved.
Keywords:
Vietnam
Cuu Long Basin
Petroleum composition
Biological markers
Lacustrine source rocks
1. Introduction
The petroleum reserves of Vietnam are considerable, with
proven reserves of oil (in 2006) amounting to 2.5 billion barrels and
193 billion cubic metres of gas (in 2005). Annual production in
2005 was estimated at 146 million barrels of oil (400,000 barrels/
day) and 6.342 billion cubic metres of gas (CIA, 2007). Resource
assessments vary, however, and the gures given by Nguyen (2006)
that are used below add up to somewhat more than the estimates
by the CIA cited above.
* Corresponding author. Tel.: 45 3814 2459; fax: 45 3814 2050.
E-mail address: jbk@geus.dk (J.A. Bojesen-Koefoed).
0264-8172/$ see front matter 2008 Elsevier Ltd. All rights reserved.
doi:10.1016/j.marpetgeo.2008.04.011
900
Fig. 1. Location map. Left: overview, study area shown by red rectangle; right: Cuu Long Basin areas corresponding to red rectangle shown in overview map. Oil eld locations are
shown.
2. Geology
The Cuu Long Basin is an elongated WSWENE trending basin
that covers an area of approximately 100 by 250 km, situated off the
south coast of Vietnam. It is one of a series of Tertiary age basins
along the Vietnamese coast that also includes the Song Hong, Phu
Khanh, and Nam Con Son Basins (Andersen et al., 2005; Canh et al.,
1994; Fyhn et al., 2009; Lee and Watkins, 1998; Lee et al., 2001). The
Cuu Long Basin is a typical rift basin, underlain by fractured and
heavily weathered Mesozoic basement (granites and granodiorites). The sedimentary succession consists of a Palaeogene syn-rift
package separated from a Neogene post-rift succession by an
inversion unconformity of latest Oligocene to earliest Miocene age.
The inversion unconformity marks the transition from a tectonic
regime dominated by rifting to one characterised by regional
subsidence. The syn-rift succession (EoceneOligocene) is made up
of terrigenous clastic rocks that include lacustrine and uvial
deposits and coals. The late post-rift succession consists of thick,
basinward prograding and dipping clinoforms of paralic or shallow
marine sediments (Lee et al., 2001). Organic-rich lacustrine
deposits as well as coals that may serve as petroleum source rocks
are present in the syn-rift succession. Lacustrine source rocks either
directly onlap the main reservoirs in fractured and weathered
basement, or have been brought into juxtaposition by faulting. Less
important petroleum reservoirs are present in Oligocene and
Miocene age clastic rocks of the post-rift succession.
3. Samples and methods
A total of nine oil samples from the Cuu Long Basin were analysed. They were non-pressurised test oils without detailed information regarding reservoir type or depth. The samples were
collected from the following elds (Fig. 1): Black Lion/Sutu-Den
(two samples), Sunrise/Rang ong (two samples), White Tiger/Bach
Ho (two samples), and Dragon/Rong (three samples). Aliquots were
Sample
#
Asphaltenes
(%)
Saturates
(%)
Aromatics
(%)
NSOs
(%)
Sat/
Aro
Pristane/
Phytane
Dragon
Dragon
Dragon
Black Lion
Black Lion
Sunrise
Sunrise
White
Tiger
White
Tiger
8679
8680
8681
8683
8684
8685
8686
9124
0.8
0.1
1.2
2.5
2.3
1.0
0.3
2.9
84.0
93.2
85.7
77.4
76.1
83.2
84.3
66.6
9.3
4.6
7.6
11.8
11.4
8.6
9.0
13.1
6.7
2.2
6.8
10.8
12.5
8.1
6.6
20.3
9.1
20.1
11.3
6.6
6.7
9.6
9.4
5.1
2.06
2.32
2.04
2.60
2.59
2.18
2.02
2.25
9125
0.6
83.6
8.6
7.8
9.7
2.01
left at room temperature until stable. Asphaltenes were precipitated by addition of a 40-fold excess of n-pentane. Maltene fractions were separated into saturated hydrocarbons, aromatic
hydrocarbons and heteroatomic polar compounds by Medium
Pressure Liquid Chromatography (MPLC), using a procedure
modied from Radke et al. (1980).
Gas chromatography of total hydrocarbon fractions was carried
out using a Shimadzu 2010 GC, furnished with a 25 m HP-1 WCOT
column and FID.
GCMSMS (parentdaughter) and GCMS(SIM) analyses were
performed using an Agilent 6890N gas chromatograph connected
to a Waters (Micromass) Quattro Micro GC tandem quadrupole
mass spectrometer. A Phenomenex ZB-5 capillary column
(30 m 0.25 mm i.d., lm thickness 0.10 mm) was used. The
temperature program was 30 C/min from 70 to 100 C and 4 C/
min from 100 to 308 C followed by 8 min at 308 C.
901
4. Results
Bulk compositions of the oil samples are listed in Table 1.
Asphaltene contents are low to moderate, <3%. Maltene fractions
are generally dominated by saturated hydrocarbons with subordinate proportions of heteroatomic compounds and aromatic
hydrocarbons. Thus saturated/aromatic hydrocarbon ratios are
generally high, 520. The White Tiger Field (#9124) sample has
somewhat higher proportions of asphaltenes and heteroatomic
compounds than the rest of the samples analysed, but this does not
inuence the saturated/aromatic hydrocarbon ratio, which remains
high.
Gas chromatograms generally show asymmetric bimodal,
heavy-end skewed normal alkane distributions that range at least
to nC44, with primary maxima at approximately nC25, and
secondary maxima at approximately nC15. Baselines are essentially
at with no notable presence of unresolved components (UCM),
and only very slight odd carbon number predominance is observed
among the normal alkanes. One sample from the Dragon Field
(#8680) falls outside the general pattern in showing only slight
bimodality, with a primary maximum at approximately nC15,
a secondary maximum at nC23, and a normal alkane distribution
that does not seem to extend far beyond nC38 (Fig. 2). Pristane to
phytane ratios do not show much variation, at 2.02.6 for all
samples (Table 1).
Bishomohopane 22S/(22S 22R) isomer ratios are essentially at
equilibrium for all samples, whereas C29 sterane 20S/(20S 20R)
isomer ratios are generally at or slightly below equilibrium, suggesting that the oils were generated from early- to mid-oil-window
mature source rocks (Table 2). One sample from the White Tiger
Field (#9124) shows somewhat lower C29 sterane 20S/(20S 20R)
isomer ratio, 0.34. Ratios of Ts/(Ts Tm) show little variation, 0.75
0.81, except for the White Tiger Field (#9124) sample, that yields
a value somewhat lower, 0.56 (Table 2).
Hopane distributions are shown in Fig. 3. A common feature of
all samples is the hyperbolic decrease in abundance with increasing
carbon number of hopane homologues from C30 to C35. Except for
the White Tiger Field (#9124) sample which falls outside the
general trend, all samples show high proportions of rearranged
Fig. 2. Gas chromatography data. Numbers refer to n-alkane carbon numbers. Pr: pristane, Ph: phytane.
902
Table 2
Biological marker maturity indicators.
Field
Sample #
Sterane
C29 S/(S R)
Hopane
C32 S/(S R)
Ts/(Ts Tm)
Dragon
Dragon
Dragon
Black Lion
Black Lion
Sunrise
Sunrise
White Tiger
White Tiger
8679
8680
8681
8683
8684
8685
8686
9124
9125
0.55
0.51
0.46
0.48
0.48
0.50
0.50
0.34
0.54
0.52
0.60
0.57
0.57
0.59
0.58
0.56
0.57
0.61
0.78
0.77
0.75
0.81
0.77
0.77
0.79
0.56
0.77
Sterane C29 S/(S R): C29 regular sterane 20aaS/(20aaS 20aaR) epimer ratio.
Hopane C32 S/(S R): Bishomohopane 22S/(20S 20R) epimer ratio.
Ts/(Ts Tm): Trisnorneohopane/(Trisnorneohopane Trisnorhopane) ratio.
Ts H29
H30
Dragon
#8679
Tm
D29
O
Dragon
#8680
Dragon
#8681
Black Lion
#8683
Sunrise
#8685
White Tiger
#9124
Black Lion
#8684
Sunrise
#8686
White Tiger
#9125
H33
Fig. 3. Distribution of C27C35 hopanes. Sum of relevant GCMSMS parentdaughter transitions (m/z 370191; m/z 384191; m/z 398191; m/z 412191; m/z 426191; m/z 440
191; m/z 454191; m/z 468191; m/z 482191). Ts: trisnorneohopane; Tm: trisnorhopane; D29: C29 diahopane; H29; C29 hopane; O: oleanane; H30: hopane; and H33: trishomohopane. Note the hyperbolic decrease in abundance with increasing carbon number of extended hopanes.
H30
H30
H30
Dragon
#8679
903
Dragon
#8680
Dragon
#8681
DH03 O
G
DH30 O
DH30 O
H30
H30
H30
Sunrise
#8685
Black Lion
#8683
DH30
White Tiger
#9124
DH30 O
G
H30
DH30
O
G
H30
H30
Black Lion
#8684
Sunrise
#8686
DH30
DH30 O
White Tiger
#9125
DH30
Fig. 4. C30 pentacyclic triterpanes, GCMSMS data m/z 412191 transition. DH30: diahopane; O: oleanane; H30: hopane; and G: gammacerane.
Table 3
Biological marker facies indicators.
Field
Sample # C29 Sterane Dia/Regular Total Sterane C27/C29 Diahopane index Oleanane index Gammacerane index C23 Tricyclic/Hopane Bicadinane index
Dragon
Dragon
Dragon
Black Lion
Black Lion
Sunrise
Sunrise
White Tiger
White Tiger
8679
8680
8681
8683
8684
8685
8686
9124
9125
0.87
0.97
0.77
1.63
1.69
1.87
1.92
0.55
0.83
1.05
1.10
1.06
1.09
1.13
1.12
1.19
1.14
1.09
18.57
8.38
15.03
10.84
8.62
16.03
15.42
2.95
16.51
13.6
6.5
12.1
10.3
7.9
14.5
13.5
5.4
12.5
8.17
4.87
7.99
3.17
3.50
5.52
5.35
3.64
7.99
1.55
0.64
1.40
0.15
0.10
0.20
0.23
0.05
1.10
69.0
32.4
65.1
44.2
35.5
77.3
79.8
33.4
69.6
904
H29
Dragon
#8679
Dragon
#8680
H29
29Ts
Dragon
#8681
29Ts
DH29
DH29
M29
NSP
NG?
H29
29Ts
DH29
M29
NSP
DH29
H29
Black Lion
#8683
29Ts
H29
29Ts
NG?
NG?
NG?
H29
Black Lion
#8684
H29
Sunrise
#8685
NSP
M29
DH29
H29
Sunrise
#8686
29Ts
White Tiger
#9124
NSP
M29
29Ts
NG?
White Tiger
#9125
DH29
DH29
DH29
NG?
29Ts
DH29
NSP
M29
NSP
M29
NSP
M29
NSP
NG?
M29
NSP
M29
NG?
NG?
Fig. 5. C29 pentacyclic triterpanes, GCMSMS data m/z 398191 transition. DH29: nordiahopane; H29: norhopane; 29Ts: norneohopane; NSP: 28-norspergulane; M29: normoretane; and NG?: norgammacerane (tentatively identied).
T23
T23
Dragon
#8679
Dragon
#8680
T23
H30
Dragon
#8681
H30
H30
H30
Sunrise
#8685
Black Lion
#8683
H30
H30
White Tiger
#9124
T23
T23
T23
H30
H30
Black Lion
#8684
Sunrise
#8686
T23
White Tiger
#9125
T23
H30
T23
Fig. 6. Distribution of C19C33 tricyclic triterpanes. Sum of relevant GCMSMS parentdaughter transitions (m/z 262191; m/z 276191; m/z 290191; m/z 304191; m/z 318191;
m/z 332191; m/z 346191; m/z 360191; m/z 374191; m/z 388191; m/z 402191; m/z 416191; m/z 430191; m/z 444191; m/z 458191). C30 hopane (m/z 412191) included for
comparison. T23: C23 tricyclic terpane; H30: hopane.
D27 S27
+
D29
Dragon
#8679
905
Dragon
#8680
Dragon
#8681
Black Lion
#8683
Sunrise
#8685
White Tiger
#9124
Black Lion
#8684
Sunrise
#8686
White Tiger
#9125
S28
S29
Fig. 7. Distribution of C27C29 steranes. Sum of relevant GCMSMS parentdaughter transitions (m/z 372217; m/z 386217; m/z 400217). D27: C27 diasteranes; D29:
C29 diasteranes; S27: C27 regular steranes; S28: C28 regular steranes; and S29: C29 regular steranes.
phytane ratios and the conspicuous hyperbolic decrease in abundance with increasing carbon number of hopane homologues from
C30 to C35 are, if not typical, at least very commonly found in
lacustrine deposits. The TPP-index of Holba et al. (2003) is equal to
1 in all samples which in combination with tricyclic triperpanes
T26/T25 ratios >1 (Fig. 10; Peters et al., 2005) provide a strong
indication of a lacustrine origin. This is supported by the absence of
marine C30 desmethyl steranes (i.e. 24-n-propylcholestanes) and
marine diatom-derived norcholestanes.
Despite an overall common origin from lacustrine source rocks,
considerable differences are found in the detailed biological marker
distribution. Hence, based on a variety of such data, oils from the
individual elds can be more or less clearly distinguished, and be
compared to other oil or source rock samples to establish potential
genetic relationships. Moreover, since the oils studied here all show
comparable levels of thermal maturity; differences can be assumed
to reect variations in organic facies of the source rocks.
Conspicuous variations are shown by the relative abundance of
tricyclic to pentacyclic terpanes (Fig. 6). In Table 3, this is represented by the T23/H30 ratio, which varies over an order of
magnitude, but other ratios may be devised as well that show the
same pattern. Tricyclic triterpanes are generally held to be marine
indicators since their occurrence has been linked to prasinophycean algae (e.g. De Grande et al., 1993) but it is also clear that the
abundance of tricyclic terpanes in nearly all kinds of oils and
sediments is much too high to be accounted for by input from such
algae, and other, presently unknown sources must exist (Peters
et al., 2005, and references therein). So although marine shale oils
in general are characterised by a high proportion of tricyclic terpanes, the partially orphaned nature of this compound class
means that it cannot alone be used as an indicator of marine
deposition. In light of the absence of other accepted marine indicators in the Cuu Long Basin oils, and the strong evidence for
lacustrine source rocks, the variation in tricyclic terpanes observed
here is regarded as a reection of differences in depositional
environment other than that caused by marine inuence. Irrespective of the underlying cause, the relative abundance of tricyclic
triterpanes clearly distinguish the Black Lion Field and the Sunrise
Field from each other and from the Dragon and the White Tiger
Fields, that in turn, however, are not clearly mutually distinguished
since one White Tiger Field sample (#9125) is very similar to the
Dragon Field samples whereas the other sample (#9124) is markedly different from any other oil sample analysed. In several other
respects, including thermal maturity, the #9124 sample shows
unexpected features.
Variations are observed in several other parameters (Table 3).
Oleanane, which is usually accepted as a marker of angiosperm
higher land plant contributions to kerogen (see Nytoft et al., 2002,
for in-depth discussion and references), and as such is to be
expected in oils generated from Palaeogene lacustrine source rocks,
shows similar ability to distinguish the individual elds, in particular when combined with the distribution of tricyclic terpanes
(Fig. 11). The variation in the proportions of oleanane probably
reects minor variations in depositional environment and/or
organic matter input within the lakes where the source rocks were
deposited. Gammacerane, which when present in high proportions
C28
Dragon
Black Lion
Sunrise
White Tiger
C27
C29
906
Dragon
#8679
Dragon
#8680
2
3
Dragon
#8681
9
Black Lion
#8683
2
1
Sunrise
#8685
White Tiger
#9124
9
2
Black Lion
#8684
3
1
3
91
Sunrise
#8686
White Tiger 3
#9125
3
91
Fig. 9. Distribution of methylphenanthrenes, GCMS(SIM) m/z 192. Note considerable variation in methylphenanthrene isomers between individual elds. In particular the Sunrise
Field samples show a very unusual isomer distribution. Peak numbers refer to isomer name (e.g. 3 3-methylphenanthrene).
1
Dragon Field
Black Lion Field
Sunrise Field
White Tiger Field
na
te
0.8
0.6
C
ar
bo
0.4
rl
Ma
0.2
hal
es
rin
Ma
Lacustrine
0
0.5
0.7
0.9
1.1
1.3
1.5
1.7
1.9
16
Oleanane index
12
10
Dragon Field
Black Lion Field
Sunrise Field
White Tiger Field
14
1.6
1.2
0.8
0.4
Dragon Field
Black Lion Field
Sunrise Field
White Tiger Field
4
0
0.4
0.8
1.2
1.6
Fig. 11. C23 tricyclic terpane to hopane ratio versus oleanane index. The Black Lion and
Sunrise Fields are clearly distinguished from each other as well as from the Dragon and
White Tiger Fields, which in turn are mutually imperfectly separated. The #9125
sample collected from the White Tiger Field shows afnity to the Dragon Field samples,
whereas the #9124 sample from the White Tiger Field shows little afnity to any other
sample analysed.
9
Dragon Field
Black Lion Field
Sunrise Field
White Tiger Field
0.4
0.8
1.2
1.6
28-norspergulane/normoretane
Gammacerane index
907
of such source rocks and the petroleum that may be generated from
them. The geochemical characteristics of source rocks from the
different lake types vary widely, and the variability of characteristics within each group is also considerable. However, judging from
the characteristics noted for the Cuu Long Basin oils compared
to the geochemical criteria established by Carroll and Bohacs
(2001), the lacustrine source rocks from which they were generated
were probably deposited in overlled to balanced-ll lake types,
according to the classication scheme of Bohacs et al. (2000).
Comparison of the characteristics of the Cuu Long Basin oils
studied here to other published oil compositional data from Vietnam shows that they share the overall lacustrine character with the
B-10 oil from the Song Hong Basin (Petersen et al., 2004), although
slight differences can be noted. Conversely, the Cuu Long Basin oils
are markedly different from the seepage oils from Dam Thi Nai on
the coast of south-central Vietnam (Bojesen-Koefoed et al., 2005).
6. Conclusion
3
4
10
12
14
16
Oleanane index
Fig. 12. Oleanane index versus gammacerane index. The Black Lion and Sunrise Fields
are clearly distinguished from each other as well as from the Dragon and White Tiger
Fields, that in turn are mutually imperfectly separated. The #9125 sample collected
from the White Tiger Field shows afnity to the Dragon Field samples, whereas the
#9124 sample from the White Tiger Field shows little afnity to any other sample
analysed.
The Cuu Long Basin in the south Vietnam offshore is the most
prolic and productive petroliferous basin in Vietnam. A series of
nine oil samples collected from wells in the Cuu Long Basin were
analysed. The samples represent four different producing elds: the
Dragon (Rong), Black Lion (Sutu-Den), Sunrise (Rang ong) and
White Tiger (Bach Ho) Fields. The data presented here represent to
the best of our knowledge the most comprehensive publicly
available systematic data on oil compositions in the Cuu Long Basin.
The oils are highly parafnic, wax-rich, not biodegraded, and
show similar levels of thermal maturity. Despite overall similarity
of the oils, a combination of several biological marker parameters
allows the individual elds to be distinguished from each other,
although samples from the Dragon and White Tiger Fields in
a number of respects show very similar characteristics this may
reect their relatively close geographical proximity.
Biological marker data suggest that all of the oils were generated
from lacustrine source rocks that are known to be present in the
908
Oligocene syn-rift portion of the basin ll. The geochemical characteristics of the oils suggest that they were generated from source
rocks deposited in overlled to balanced-ll lake types according to
the classication of Bohacs et al. (2000) and Carroll and Bohacs
(2001). The Cuu Long Basin oils show overall similarity to the
lacustrine B-10 oil from the Song Hong Basin, but are distinctly
different from the Dam Thi Nai oil known from seepages on the
coast of south-central Vietnam.
Acknowledgements
This study is a part of the DANIDA-sponsored ENRECA-project:
Integrated analysis and modelling of geological basins in Vietnam
and assessment of their hydrocarbon potential which is a cooperative project between the Geological Survey of Denmark and
Greenland (GEUS), the University of Copenhagen, Vietnam Petroleum Institute (VPI), PetroVietnam, Hanoi University of Mining and
Geology (HUMG) and Hanoi University of Science (HUS). Laboratory
assistance by Ditte Kiel-Duhring and Carsten Guvad is gratefully
acknowledged. M.B.W. Fyhn provided useful comments to an
earlier version of the manuscript. Location map (Fig. 1) was drafted
by Jette Halskov. We thank S.D. Killops for a helpful review that
served to improve the quality of the paper. VPI, PetroVietnam and
GEUS are thanked for procurement of samples and permission to
publish this paper.
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