Geological Society, London, Special Publications
Monsoon control over erosion patterns in the Western Himalaya:
possible feed-back into the tectonic evolution
Peter D. Clift, Liviu Giosan, Andrew Carter, Eduardo Garzanti, Valier Galy, Ali R. Tabrez,
Malcolm Pringle, Ian H. Campbell, Christian France-Lanord, Jurek Blusztajn, Charlotte Allen,
Anwar Alizai, Andreas Lückge, Mohammed Danish and M.M. Rabbani
Geological Society, London, Special Publications 2010; v. 342; p. 185-218
doi:10.1144/SP342.12
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Massachusetts Institute of Technology on 3 September 2010
© 2010 Geological Society of
London
Monsoon control over erosion patterns in the Western Himalaya:
possible feed-back into the tectonic evolution
PETER D. CLIFT1*, LIVIU GIOSAN2, ANDREW CARTER3, EDUARDO GARZANTI4,
VALIER GALY2, ALI R. TABREZ5, MALCOLM PRINGLE6, IAN H. CAMPBELL7,
CHRISTIAN FRANCE-LANORD8, JUREK BLUSZTAJN2, CHARLOTTE ALLEN6,
ANWAR ALIZAI1, ANDREAS LÜCKGE9, MOHAMMED DANISH5 & M.M. RABBANI5
1
School of Geosciences, University of Aberdeen, Aberdeen, AB24 3UE, UK
2
Woods Hole Oceanographic Institution, Woods Hole, MA 02543, USA
3
School of Earth Sciences, University and Birkbeck College London, Gower Street,
London, WC1E 6BT, UK
4
Dipartimento Scienze Geologiche e Geotecnologie, Universita’ di Milano-Bicocca,
Piazza della Scienza 4 – 20126 Milano, Italy
5
National Institute for Oceanography, Clifton, Karachi 75600, Pakistan
6
Department of Earth, Atmospheric and Planetary Sciences, Massachusetts Institute of
Technology, Cambridge, Massachusetts, USA
7
Research School of Earth Sciences, The Australian National University, Canberra,
A.C.T. 0200, Australia
8
CRPG-CNRS, BP 20, 15 rue Notre Dame des Pauvres, 54501 Vandoeuvre les Nancy, France
9
Bundesanstalt für Geowissenschaften und Rohstoffe (BGR), Stilleweg 2,
D-30655 Hannover, Germany
*Corresponding author (email: p.clift@abdn.ac.uk)
Abstract: The Indus Delta is constructed of sediment eroded from the western Himalaya and since
20 ka has been subjected to strong variations in monsoon intensity. Provenance changes rapidly at
12–8 ka, although bulk and heavy mineral content remains relatively unchanged. Bulk sediment
analyses shows more negative 1Nd and higher 87Sr/86Sr values, peaking around 8 –9 ka. Apatite
fission track ages and biotite Ar–Ar ages show younger grains ages at 8– 9 ka compared to at
the Last Glacial Maximum (LGM). At the same time d13C climbs from – 23 to – 20‰, suggestive
of a shift from terrestrial to more marine organic carbon as Early Holocene sea level rose. U–Pb
zircon ages suggest enhanced erosion of the Lesser Himalaya and a relative reduction in erosion
from the Transhimalaya and Karakoram since the LGM. The shift in erosion to the south correlates
with those regions now affected by the heaviest summer monsoon rains. The focused erosion along
the southern edge of Tibet required by current tectonic models for the Greater Himalaya would be
impossible to achieve without a strong summer monsoon. Our work supports the idea that although
long-term monsoon strengthening is caused by uplift of the Tibetan Plateau, monsoon-driven
erosion controls Himalayan tectonic evolution.
Supplementary material: A table of the population breakdown for zircons in sands and the
predicted Nd isotope composition of sediments based on the zircons compared to the measured
whole rock value is available at http://www.geolsoc.org.uk/SUP18412
The relationships between climate, continental erosion and mountain building continue to be debated
and are central to understanding how the solid
planet and its atmosphere have interacted over
long periods of geological time. In particular, the
links between mountain building in Cenozoic Asia
and the intensification of the monsoon are presently
unclear, with the different processes feeding back on
each other. Although climate modelling has shown
that a wide, high Tibetan Plateau is important to
From: Clift, P. D., Tada, R. & Zheng, H. (eds) Monsoon Evolution and Tectonics –Climate Linkage in Asia.
Geological Society, London, Special Publications, 342, 185–218.
DOI: 10.1144/SP342.12 0305-8719/10/$15.00 # The Geological Society of London 2010.
186
P. D. CLIFT ET AL.
maintaining a strong monsoon circulation (An et al.
2001; Kitoh 2004) it is also clear that monsoon
strength has varied greatly over millennial to
orbital timescales, driven by solar factors either
directly or via its influence on the intensity of northern hemispheric glaciation (Clemens et al. 1991;
Wang et al. 2005). Feedbacks may work in both
direction however. Recent geomorphological
and thermochronometric work indicates that the
location of active faulting in mountains and thus
orogenic architecture is controlled by climate zonation (Hodges et al. 2004; Wobus et al. 2003), at least
as much as by plate tectonic processes. Both wedge
and channel-flow models proposed to explain the
origin of the Greater Himalaya (Nelson et al.
1996; Robinson et al. 2003; Harris 2007) require
focused erosion driven by monsoon rains to allow
exhumation of deeply buried metamorphic rocks.
If we are to understand what influence climate
alone has on erosion (and thus on tectonics) then
we need to isolate the climate signal from tectonic
overprints. One way to do this is to study changes
in erosion on timescales that are too short to allow
tectonism to be an important influence.
In this study we assess the response of the Indus
river basin to the intensification of the South Asian
monsoon since the Last Glacial Maximum (LGM),
around 20 ka. Cave records in Arabia (Fleitmann
et al. 2003), together with Indian lake sediments
(Enzel et al. 1999) and marine cores (Staubwasser
et al. 2002) now show that the summer monsoon
strengthened as global climate warmed between
the LGM (c. 20 ka) and the Early Holocene
c. 8 ka. Earlier sedimentological work in the
Bengal delta demonstrated that the intensification
of the summer monsoon correlated with a great
increase in the rate of sediment delivery to the
delta during the Early Holocene, c. 8 ka (Goodbred
& Kuehl 2000). This is suggestive of greatly
enhanced erosion and sediment transport rates
in the source regions, presumably driven by the
influence of stronger summer monsoon rains, as
the speed of response rules out a tectonic trigger.
Indeed studies of landsliding in the western Himalaya show that large scale mass wasting correlates
with periods of stronger monsoon (Bookhagen
et al. 2005), consistent with the delta records.
Recently we reported that the Indus delta
also prograded seawards during the onset of the
Holocene (Giosan et al. 2006), that is, at a time of
rapid sea level rise. This observation requires a
major increase in the flux of sediment to the delta
to balance the increasing accommodation space
caused by sea level rise. Crucially, the delta was
prograding southwards during the 8–12 ka period
when rates of eustatic sea level rise were greatest
(Camoin et al. 2004). Most recently, Clift et al.
(2008) used a combination of bulk sediment Nd
isotopes, single grain U –Pb zircon ages and
Ar –Ar muscovite mica ages to argue for a sharp
increase in the relative erosional flux from the
Lesser Himalaya during the Early Holocene. In
this paper we test their hypothesis that intensification of the summer monsoon resulted in much
heavier rain along the southern edge of the Greater
Himalaya and especially over the Lesser Himalaya.
We do this using a series of additional geochemical
proxies to assess the source of sediment at any given
time and the changing environmental conditions in
the Indus basin, which can then be compared to
established climate records.
Sampling
Samples were taken from four boreholes drilled in
the delta (Fig. 1). Although total recovery was not
high material was recovered from most parts of
the drilled sections, thus allowing a relatively continuous erosion record to be reconstructed (Fig. 2).
At Keti Bandar drilling penetrated the ravinement
surface that forms the base of the modern Indus
delta and recovered Pleistocene sand deposited
during the LGM (Clift et al. 2008). At all other
sites only the Holocene to Younger Dryas sections
were recovered. Ages of deposition were calculated
from accelerator mass spectrometer (AMS) 14C
dating of organic materials made at the National
Ocean Sciences Accelerator Mass Spectrometry
facility (NOSAMS, Woods Hole Oceanographic
Institution) (Clift et al. 2008). Radiocarbon ages
from below the deltaic sediments were 28.7 and
38.9 ka, suggesting reworking and mixing of older
sediment prior to transgression after 20 ka. The
Keti Bandar section shows two coarsening-upward
cycles, separated by a transgressive mud deposited
after c. 8 ka (Fig. 2). The cores were sampled both
for sands, which were mostly used for single grain
thermochronological methods, and for clays that
were used for organic carbon analysis.
Analytical methods
A number of different provenance methods were
used in order to establish a matrix of constraints,
since typically one or two methods were insufficient
to define a sediment source area for any given sand
sample. In this study, we analysed the sediments
using classical sand petrography, Sr isotopes,
apatite and zircon fission track, Ar –Ar single
biotite grain dating and additional U –Pb zircon
dating, beyond the samples already considered by
Clift et al. (2008). In addition, we selected clay
samples for organic carbon isotope geochemistry
in order to constrain the general composition of
the vegetation in the Indus basin. Here we describe
MONSOON CONTROL OVER EROSION
HK
187
KK
K
NP
Tarbela
Dam
LA
35°
N
ZA
Islamabad
m Ch
llu
vi
Ra
ks
Je
GH
ali
Siw
b
a
en
STD
LH
MBT
MCT
Garhwal
MFT
Sutlej
us
Ind
rt
Sukkur
ar
De
se
Thatta
Keti
Bandar
Th
Karachi
30°
N
Gularchy
Jati
25°
N
Arabian Sea
70°E
75°E
Fig. 1. Shaded topographic map of the Indus drainage basin, showing the location of the boreholes in the delta,
the major tributaries of the modern river and the principal sediment source terrains (HK, Hindu Kush; K, Kohistan;
NP, Nanga Parbat; ZA, Zanskar; LA, Ladakh; KK, Karakoram; GH, Greater Himalaya; LH, Lesser Himalaya; MBT,
Main Boundary Thrust; MFT, Main Frontal Thrust; MCT, Main Central Thrust; STD, South Tibet Detachment) [from
Clift et al. (2008)]. White dots indicate boreholes. Black dots with white rim indicate place name mentioned in the text.
Reproduced with the permission of the Geological Society of America.
the methods employed to reconstruct the evolving
character of the Indus delta.
Mineralogy
All nine samples analysed for petrography from
the Keti Bandar and Thatta cores were very finegrained sands containing variable amounts of bioclasts. In each sample, 400 points were counted by
the Gazzi-Dickinson method (Ingersoll et al.
1984). Data are presented in Tables 1 and 2. Traditional ternary parameters and plots (Dickinson
1985) were supplemented, specifically as lithic
grains are concerned, by an extended spectrum of
key indices. Metamorphic rock fragments were
classified according to both composition and
metamorphic rank, mainly inferred from degree
of recrystallization of mica flakes (Garzanti &
Vezzoli 2003). Very low to low-rank metamorphic
lithics, for which protolith can still be inferred,
were subdivided into metasedimentary (Lms)
and metavolcanic (Lmv) categories. Medium to
high-rank metamorphic lithics were subdivided
instead into felsic (metapelite, metapsammite,
metafelsite; Lmf) and mafic (metabasite; Lmb)
categories.
188
P. D. CLIFT ET AL.
Fig. 2. Diagram shows the stratigraphy of the sediment cored at each of the drilling sites considered in this study,
as shown in Figure 1. Each log shows the depth, proportion of the section recovered by drilling (black equates to
recovery), the age control points constrained by 14C AMS dating of organic materials, as well as the location of samples
selected from isotopic and thermochronological analysis. TD, total depth. Reproduced with the permission of the
Geological Society of America.
Heavy minerals were separated from the veryfine to fine sand fraction (63–250 mm), treated
with acetic acid and sodium dithionite, by centrifuging in sodium metatungstate (density c. 2.9 g
cm23). From each sample, 200– 250 transparent
heavy minerals were counted in grain mounts by
the ‘ribbon-counting’ or ‘Fleet’ methods (Mange
& Maurer 1992). The abundance of total
(transparent þ opaque þ turbid) and transparent
heavy minerals in the sediment were expressed by
the ‘Heavy Mineral Concentration’ (HMC) and
‘transparent Heavy Mineral Concentration’
(tHMC) indices (Garzanti & Andò 2007).
Sr isotope analysis
Samples from both the Keti Bandar and Gularchy
boreholes were sampled for Sr analysis. Sr analysis
was only performed on samples that had previously
been analysed for Nd isotopes (Clift et al. 2008).
Sr can be used for provenance work, but because
it is mobilized during chemical weathering is less
definitive than Nd isotopes. However, this characteristic can be used to effect because Sr variability
in the absence of provenance changes has been
interpreted to reflect changing intensities of chemical weathering (Palmer & Edmond 1991; Blum &
Erel 1995). In particular, the Sr isotope composition of clay reflects the Sr characteristics of the
groundwater in which they were formed, rather
than the composition of the source rock (McBride
1994; Derry & France-Lanord 1996). Assuming
that the clays have not been affected by diagenesis
(unlikely in such young materials) the Sr isotopes
can be used to track the evolving intensity of silicate
weathering. However, in this setting the Nd isotope
composition is known to change especially at
14 –8 ka and so changes in Sr at those times may
be mostly provenance driven.
Samples were accurately weighed into teflon
screw-top beakers and dissolved using HF-HNO3HCl. Sr samples were separated in 2.5 N HCl
Table 1. Bulk mineralogy data for selected sands from the Keti Bandar and Thatta boreholes derived from point counting of microcopic grain mounts
Site
n/a
KB-5-2
TH-10-8
KB-20-1
KB-23-2
KB-26-2
KB-30-1
KB-34-4
KB-40-5
KB-41-2
Delta
Keti Bandar
Thatta
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Depth
(m)
Age
(ka)
Mean grain
size
(micron)
Q
KF
P
15
31
58
67
76
88
102
118
120
0
0.18
7.14
9.21
9.65
10.64
12.26
14.23
20.00
20.00
119
82
93
87
39
51
38
73
85
82
41
40
38
46
40
36
37
41
39
46
7
10
11
10
10
8
11
5
12
8
9
12
15
10
10
8
8
15
14
14
Lvf Lvm Lcc Lcd Lp Lch Lms Lmv Lmf Lmb Lu Mu Bi
0
0
1
1
0
0
2
1
1
1
0
0
0
0
0
0
0
0
1
1
8
8
6
11
6
7
7
6
0
0
3
3
3
3
1
2
2
2
4
4
3
1
1
1
2
0
1
5
1
0
1
0
0
0
0
0
0
1
0
0
7
3
4
4
4
2
2
5
4
6
1
1
4
1
1
1
1
4
2
2
3
5
5
5
5
2
3
4
5
5
2
0
1
0
0
0
0
0
1
0
0
0
0
0
0
0
0
0
0
0
1
4
2
2
4
7
6
4
4
2
2
11
8
5
15
25
19
8
9
7
Dense Total
minerals
11
3
2
2
1
2
1
0
3
2
100
100
100
100
100
100
100
100
100
100
MONSOON CONTROL OVER EROSION
Sample
Abbreviations: Q, quartz; KF, K-felspar; P, plagioclase; Lvf, lithic felsic volcanic; Lvm, lithic mafic volcanic; Lcc, calcite carbonate lithic; Lcd, dolomite carbonate lithic; Lp, shale/silt; Lch, chert; Lmv,
metavolcanic lithics; Lmf, felsic metamorphic lithics; Lmb, basic metamorphic lithics; Lu, ultramafic lithics; Mu, muscovites; Bi, biotites.
189
190
Table 2. Heavy mineral data for selected sands from the Keti Bandar and Thatta boreholes derived from point counting of microcopic grain mounts
Sample
Depth
(m)
Age
(ka)
% of
heavy
minerals
in 63 – 250
mm
fraction
% of
heavy
minerals
transparent
Delta
Keti Bandar
Thatta
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
n/a
KB-5-2
TH-10-8
KB-20-1
KB-23-2
KB-26-2
KB-30-1
KB-34-4
KB-40-5
KB-41-2
0
14
30
58
67
77
78
101
118
120
0
0.18
7.14
9.21
9.65
10.64
10.77
14.20
20.00
20.00
9.6
3.0
4.9
3.9
0.9
1.3
1.4
4.0
4.3
4.3
8.0
2.7
3.9
3.4
0.7
1.1
1.2
3.2
3.8
3.6
%
%
%
Total zircon tourmaline rutile sphene
transparent opaque turbid
83
91
79
87
83
88
84
81
88
84
10
1
6
3
2
1
4
3
5
3
8
9
15
10
15
11
12
16
8
13
100
100
100
100
100
100
100
100
100
100
0
0
0
1
0
0
0
0
0
2
2
3
2
3
2
2
2
3
2
0
1
1
0
1
2
0
1
0
0
0
bluegreen
greenbrown/
green
hornblende
brown
red
hornblende
hornblende hornblende
2
2
0
3
2
4
1
1
3
1
39
45
33
39
34
38
34
36
47
51
4
1
5
2
4
5
4
2
0
4
3
2
2
4
0
1
2
1
3
2
2
0
0
0
0
0
0
0
0
0
Site
Sample
tremolite
actinolite
green
augite
diopside/
hedembergite
enstatite
hypersthene
epidote
clinozoisite
zoisite
other
epidotes
chloritoid
garnet
staurolite
kyanite
sillimanite
Total
Delta
Keti Bandar
Thatta
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
n/a
KB-5-2
TH-10-8
KB-20-1
KB-23-2
KB-26-2
KB-30-1
KB-34-4
KB-40-5
KB-41-2
0
0
0
0
2
2
1
0
0
0
2
3
8
6
13
7
8
5
3
4
0
0
0
0
0
0
0
2
0
0
2
4
7
5
4
4
8
4
0
1
0
0
0
0
0
0
1
0
0
0
1
3
2
2
1
1
1
1
0
1
21
28
22
26
19
25
28
25
32
24
1
1
1
1
1
0
0
0
0
0
3
0
0
1
0
2
0
1
1
1
0
0
0
1
0
0
0
1
1
0
0
0
0
2
1
0
0
0
0
0
12
2
13
4
5
5
3
11
4
4
1
1
0
0
1
1
0
1
0
0
1
1
1
3
3
1
0
0
0
1
1
0
1
1
2
1
0
2
0
0
100
100
100
100
100
100
100
100
100
100
P. D. CLIFT ET AL.
Site
MONSOON CONTROL OVER EROSION
using Bio-Rad AG50W X8 200-400 mesh cation
exchange resin using standard column methods.
They were analysed on a by Finnigan ‘Neptune’
multi-collector inductively coupled plasma mass
spectrometer (MC-ICP-MS) at Woods Hole
Oceanographic Institution. Sample measurements
were normalized to 86Sr/88Sr ¼ 0.1194 and referenced to a value of 0.710240 for NBS987 standard.
Results are provided in Table 3.
Organic carbon analysis
Total organic carbon content (TOC) and stable isotopic composition of the bulk organic matter (d13C)
were determined for 20 samples taken exclusively
from the Keti Bandar borehole (Fig. 1). A detailed
description of the analytical method can be found
in Galy et al. (2007a). Indus delta sediments
contain significant amounts of detrital carbonates
including dolomite. TOC and isotopic measurements must therefore be performed on decarbonated
sediments. Efficient dolomite dissolution was
achieved through 1 hr leaching with 4 wt% HCl at
80 8C. After 50 8C oven drying, the organic carbon
content and stable isotopic composition were determined by EA-IRMS (elemental analysis – isotope
ratio mass spectrometry). organic carbon solubilization during acid treatment was taken into
account following the approach described by Galy
et al. (2007a). The overall 2s uncertainty associated
with the TOC and d13C determination is respectively 0.02% and 0.25‰. Results of the carbon
isotope analysis are provided in Table 4.
Major and trace element analysis
Major and trace element concentrations for the
muds which were also measures for carbon isotopes
were measured respectively by Inductively Coupled
Plasma Atomic Emission Spectrophotometry
(ICP-AES) and Inductively Coupled Plasma Mass
Spectrometry (ICP-MS) at the Service d’Analyse
des Roches et des Minéraux (CRPG-Nancy,
France) on bulk sediment after lithium metaborate
fusion. Results of the element analysis are provided
in Table 4.
Fission track analyses
In this study we employed the fission-track method
applied to apatite, which records cooling through
c. 125 –60 8C over timescales of 1– 10 Ma and to
zircon which records cooling through c. 200 8C
(Green 1989). Fission-track analysis was performed
at University College, London, UK using five
samples, one of which, dating from the LGM, was
analysed for both apatite and zircon. Polished
grain mounts were etched with 5N HNO3 at 20 8C
191
for 20 seconds to reveal the spontaneous fission
tracks. Subsequently, the uranium content of each
crystal was determined by irradiation, which
induced fission of 235U. The induced tracks were
registered in external mica detectors. The samples
for this study were irradiated in the thermal facility
of the Hifar Reactor at Lucas Heights, Australia.
The neutron flux was monitored by including
Corning glass dosimeter CN-5, with a known
uranium content of 11 ppm, at either end of the
sample stack. After irradiation, sample and dosimeter mica detectors were etched in 48% HF at
20 8C for 45 minutes. Only crystals with sections
parallel to the c-axis were counted, as these crystals
have the lowest bulk etch rate. To avoid biasing
results through preferred selection of apatite crystals, the samples were systematically scanned and
each crystal encountered with the correct orientation
was analysed, irrespective of track density. The
results of the fission-track analysis are presented
in Table 5.
Ar –Ar mica dating
Single crystal 40Ar/39Ar laser-fusion analyses were
performed on biotite grains separated from two
sands (KB-41-2, from the LGM deposits at Keti
Bandar, and TH-4-6 from c. 6.4 ka sand at Thatta)
at the Massachusetts Institute of Technology
(MIT). Biotites from a modern sample of the
Indus at Thatta were previously published by Clift
et al. (2004). Prior to analysis, samples were
irradiated in the C5 position of the McMaster
University Nuclear Reactor, Canada, using 1 mm
Cd shielding for four hours at a power level of
2 MW. After fusion with an Ar-ion laser, the released gases were purified for 10 minutes with two
Al –Zr getters operated at 400 8C and room temperature, respectively, and then admitted to an
MAP 215-50 mass spectrometer for Ar isotopic
analysis using a Johnson MM-1 electronic multiplier operated at a gain of about 10 000. The conversion efficiency of 39K to 39Ar was monitored using
sanidine from the Taylor Creek rhyolite (TCR-2a)
assuming an age of 28.34 Ma (Renne et al. 1998),
and is known to better than 0.3% (1s). Corrections
for neutron-induced interferences, determined using
Fe-doped kalsilite glass and optical CaF2, were
0.00039 for 40Ar/39ArK, 0.01243 for 38Ar/39ArK,
0.000672 for 39Ar/37ArCa, 0.000033 for 38Ar/
37
ArCa and 0.00028 for 36Ar/37ArCa. Final data
reduction was conducted with the program ArArCalc (Koppers 2002); results are shown in Table 6.
U – Pb zircon dating
U –Th –Pb isotopic compositions of zircon grains
were analysed at the Australian National University,
192
Table 3. Sr isotopic data from Keti Bandar and Gularchy boreholes. Matching Nd isotope data and 14C ages are from Clift et al. (2008). See Figure 1 for locations
Sample number
Fine Sand
Fine Sand
Clay
Clay
Silt
Clay
Fine Sand
Sand
Sand
Sand
Location
Depth
(m)
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Keti Bandar
Gularchy
Gularchy
Gularchy
14.0
55.0
61.0
92.0
97.0
108.0
117.0
11.3
26.2
47.5
14
C Age
(ka)
0.21
8.72
9.42
12.20
12.91
13.73
28.70
2.65
6.42
10.94
Age 1s
(ka)
Nd143/Nd144
1Nd
0.00
0.15
0.20
0.32
0.32
0.37
0.00
0.08
0.08
0.18
0.511947
0.511858
0.511986
0.511919
0.512033
0.512000
0.512082
0.511911
0.511931
0.511962
213.5
215.2
212.7
214.0
211.8
212.4
210.8
214.2
213.8
213.2
87
Sr/86Sr
0.724512
0.727689
0.719290
0.719951
0.710671
0.714531
0.714764
0.721362
0.719811
0.725178
P. D. CLIFT ET AL.
KB-5-2
KB-19-4
KB-21-1
KB-31-2
KB-34-4
KB-37-4
KB-40-5
GUL-ZP-5-1
GUL-ZP-10-2
GUL-ZP-17-1
Lithology
Table 4. Carbon isotope and organic carbon data, together with associated major and trace element compositions from Holocene samples from Keti Bandar and
Gularchy boreholes. See Figure 1 for locations
Sample # Depth Age SiO2 Al2O3 Fe2O3 MnO MgO CaO Na2O K2O TiO2 P2O5
(%)
(%) (%) (%) (%) (%) (%) (%) (%)
(m) (a bp) (%)
7.5
20.0
26.0
26.5
37.0
44.0
55.0
59.0
67.0
70.5
92.0
96.0
100.0
100.5
107.0
110.0
112.0
117.0
118.0
119.0
112
299
1235
1314
4086
6336
8140
8560
9400
9768
12026
12446
12866
12918
13601
13916
14126
14651
14756
28700
54.23
55.93
51.48
51.16
54.02
50.67
53.44
65.28
54.32
63.43
54.09
51.49
50.27
50.67
52.36
49.58
51.51
50.89
48.04
50.07
13.47
13.42
15.04
15.22
13.69
14.84
13.67
10.94
13.72
11.04
13.60
13.78
14.13
14.49
14.04
14.84
14.18
14.58
14.86
15.23
5.46
5.35
6.42
6.51
5.64
6.38
5.62
4.00
5.67
4.79
5.66
6.11
6.04
6.21
5.88
6.42
6.11
6.35
6.68
6.63
0.09
0.09
0.10
0.10
0.09
0.10
0.10
0.07
0.10
0.08
0.09
0.09
0.09
0.09
0.09
0.09
0.09
0.10
0.10
0.10
2.94
2.87
3.32
3.39
3.04
3.42
3.00
2.22
3.04
2.35
3.03
3.20
3.46
3.38
3.48
3.45
3.56
3.61
4.36
3.49
8.48
7.27
7.28
7.17
7.92
7.71
8.14
6.72
7.26
6.81
8.38
8.76
9.39
8.28
8.30
8.64
8.09
7.91
7.67
7.69
1.74
2.14
1.83
1.88
1.83
1.73
1.79
1.87
2.35
1.94
1.82
1.90
1.91
1.87
2.02
1.81
1.96
1.98
1.88
1.74
2.54
2.54
2.94
2.98
2.53
2.88
2.64
2.09
2.49
2.08
2.62
2.68
2.71
2.83
2.76
2.89
2.82
2.89
2.95
2.97
0.66
0.69
0.74
0.75
0.81
0.72
0.71
0.60
0.71
0.63
0.68
0.69
0.70
0.71
0.70
0.71
0.70
0.70
0.72
0.72
0.14
0.16
0.16
0.16
0.19
0.15
0.15
0.14
0.15
0.16
0.15
0.16
0.16
0.15
0.16
0.15
0.16
0.16
0.14
0.15
Total
(%)
10.05
9.39
10.38
10.68
10.11
11.04
10.29
6.56
10.19
7.08
10.29
11.12
11.67
11.34
10.68
11.70
10.43
11.75
12.80
11.41
99.79
99.86
99.67
99.98
99.86
99.64
99.55
100.48
100.00
100.39
100.39
99.99
100.53
100.00
100.46
100.28
99.61
100.92
100.20
100.21
As
Ba
Be
Bi
Cd
Ce
Co
(ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm)
9.8
10.9
13.1
12.3
8.6
9.9
10.2
5.2
14.1
3.9
12.3
19.4
12.0
14.6
13.0
17.1
13.5
12.2
8.4
11.9
348.0
363.9
379.2
384.7
329.5
370.2
370.2
328.4
425.9
325.9
361.0
364.6
364.8
367.9
375.3
378.6
371.9
364.1
337.3
380.7
2.4
2.5
2.8
2.7
2.4
2.7
2.7
2.4
2.5
2.2
2.4
2.3
2.5
2.4
2.3
2.6
2.4
2.4
2.4
2.6
0.9
0.8
1.0
1.0
0.8
1.0
1.0
0.6
0.5
0.6
0.5
0.6
0.6
0.7
0.6
0.7
0.6
0.6
0.5
0.7
,L.D.
,L.D.
,L.D.
,L.D.
0.287
,L.D.
,L.D.
,L.D.
,L.D.
0.271
,L.D.
,L.D.
,L.D.
,L.D.
,L.D.
,L.D.
,L.D.
,L.D.
,L.D.
,L.D.
60.8
71.7
68.0
65.8
92.7
64.5
72.3
66.2
66.2
75.0
62.5
62.1
62.6
62.2
61.3
66.2
61.4
61.6
62.7
65.3
14.8
13.9
16.2
16.7
14.8
16.9
15.5
10.9
15.5
10.5
15.2
15.5
16.2
16.1
15.6
17.8
17.1
17.6
16.9
17.2
MONSOON CONTROL OVER EROSION
KB-3-3
KB-8-2
KB-10-2
KB-10-5
KB-13-2
KB-16-1
KB-19-3
KB-21-2
KB-23-4
KB-25-2
KB-31-1
KB-33-3
KB-34-2
KB-35-2
KB-37-4
KB-38-2
KB-38-3
KB-40-2
KB-40-3
KB-41-1
PF
(%)
(Continued )
193
194
Table 4. Continued
Cr
Cs
Cu
Dy
Er
Eu
Ga
Gd
Ge
Hf
Ho
In
La
Lu
Mo
Nb
Nd
Ni
Pb
Pr
Rb
(ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm) (ppm)
KB-3-3
KB-8-2
KB-10-2
KB-10-5
KB-13-2
KB-16-1
KB-19-3
KB-21-2
KB-23-4
KB-25-2
KB-31-1
KB-33-3
KB-34-2
KB-35-2
KB-37-4
KB-38-2
KB-38-3
KB-40-2
KB-40-3
KB-41-1
100.9
92.2
107.6
107.9
112.9
110.4
105.2
83.1
97.8
84.2
99.0
104.4
105.2
108.7
108.3
114.7
111.6
113.0
121.8
114.7
8.2
7.8
10.1
10.0
8.2
10.1
9.3
6.2
6.9
5.9
8.3
8.4
7.8
8.9
7.8
9.1
8.2
8.7
8.2
10.7
25.6
24.4
31.4
33.5
24.8
34.0
27.8
13.8
27.1
15.5
26.4
28.5
31.0
32.3
28.7
37.4
30.5
33.6
52.6
33.6
4.0
4.5
4.3
4.1
5.9
4.1
4.8
4.3
4.4
4.7
4.0
4.0
4.0
4.0
4.0
4.1
4.1
4.0
4.2
4.1
2.2
2.5
2.4
2.3
3.2
2.2
2.6
2.4
2.4
2.5
2.1
2.2
2.2
2.2
2.2
2.2
2.2
2.2
2.3
2.3
1.1
1.2
1.1
1.1
1.4
1.1
1.2
1.1
1.1
1.2
1.0
1.1
1.1
1.1
1.1
1.1
1.1
1.1
1.1
1.1
17.5
17.5
20.3
20.0
18.7
20.2
19.3
14.4
18.5
14.4
17.8
18.4
18.7
19.1
17.5
19.5
18.6
19.3
20.0
20.4
4.4
5.0
4.7
4.6
6.5
4.5
5.2
4.8
4.9
5.3
4.5
4.5
4.4
4.4
4.5
4.7
4.6
4.5
4.6
4.6
1.6
1.6
1.7
1.7
1.7
1.7
1.7
1.5
1.6
1.6
1.6
1.6
1.6
1.5
1.6
1.6
1.6
1.6
1.7
1.7
3.6
5.1
4.0
3.8
7.7
3.5
4.7
6.1
4.5
6.8
4.1
4.1
3.9
3.8
4.0
3.6
4.2
4.0
3.6
3.5
0.8
0.9
0.8
0.8
1.1
0.8
0.9
0.8
0.8
0.9
0.8
0.8
0.8
0.8
0.8
0.8
0.8
0.8
0.8
0.8
0.2
0.2
0.2
0.2
0.3
0.2
0.3
0.2
0.2
0.2
0.2
0.2
0.3
0.2
0.1
0.2
0.2
0.2
0.2
0.2
30.2
36.3
33.9
33.4
46.5
31.9
36.1
33.0
33.6
37.8
31.6
31.3
31.6
31.5
31.1
33.1
31.0
31.2
31.5
32.8
0.3
0.4
0.4
0.4
0.5
0.3
0.4
0.4
0.4
0.4
0.3
0.3
0.3
0.3
0.3
0.4
0.3
0.3
0.4
0.4
0.6
,L.D.
0.7
0.7
0.5
0.8
0.6
,L.D.
0.7
,L.D.
0.6
1.3
0.7
0.9
0.6
0.7
0.6
0.6
0.8
0.7
12.2
13.0
14.2
14.4
15.1
13.4
13.8
11.3
13.9
11.6
12.7
12.9
13.1
12.9
12.5
13.4
12.8
13.0
13.2
13.8
26.2
30.9
28.6
28.5
40.1
27.5
31.0
28.6
28.6
32.3
26.5
26.8
26.7
26.8
26.5
28.3
26.4
26.9
27.3
27.7
53.5
48.1
60.7
59.2
53.3
61.0
54.4
36.9
53.9
34.4
54.7
55.6
59.4
62.3
56.6
64.9
61.4
65.8
71.8
62.9
17.9
16.7
22.1
20.6
19.1
20.3
18.4
19.9
11.1
17.6
18.1
15.9
14.7
16.6
14.4
15.1
15.8
14.9
14.0
20.5
6.9
8.3
7.7
7.6
10.6
7.3
8.3
7.7
7.7
8.7
7.2
7.2
7.2
7.1
7.1
7.6
7.1
7.1
7.2
7.5
117.7
117.0
141.6
136.1
119.7
133.7
127.8
97.8
115.7
95.0
119.8
121.1
121.2
125.8
120.1
131.7
123.2
125.8
124.2
143.0
(Continued )
P. D. CLIFT ET AL.
Sample #
Table 4. Continued
Sb
(ppm)
Sm
(ppm)
Sn
(ppm)
Sr
(ppm)
Ta
(ppm)
Tb
(ppm)
Th
(ppm)
Tm
(ppm)
U
(ppm)
V
(ppm)
W
(ppm)
Y
(ppm)
Yb
(ppm)
Zn
(ppm)
Zr
(ppm)
TOC
(%)
d13C
(‰)
KB-3-3
KB-8-2
KB-10-2
KB-10-5
KB-13-2
KB-16-1
KB-19-3
KB-21-2
KB-23-4
KB-25-2
KB-31-1
KB-33-3
KB-34-2
KB-35-2
KB-37-4
KB-38-2
KB-38-3
KB-40-2
KB-40-3
KB-41-1
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.5
1.7
0.5
1.6
1.7
1.9
0.8
0.7
2.0
1.7
1.7
1.6
0.7
5.2
6.0
5.6
5.5
7.9
5.4
6.2
5.8
5.7
6.4
5.3
5.2
5.4
5.2
5.3
5.6
5.3
5.3
5.3
5.5
3.6
3.8
4.2
4.2
3.8
4.2
4.0
3.4
4.4
3.4
3.9
4.0
4.2
3.7
3.5
4.3
4.1
4.0
3.9
4.0
204.6
201.1
203.2
194.4
214.3
190.9
199.0
188.8
199.7
191.3
210.2
253.2
370.8
221.1
223.1
226.0
233.6
230.2
181.4
198.7
1.1
1.3
1.3
1.3
1.5
1.2
1.2
1.2
1.3
1.2
1.1
1.2
1.2
1.2
1.2
1.2
1.2
1.2
1.2
1.3
0.7
0.8
0.7
0.7
1.0
0.7
0.8
0.8
0.8
0.8
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
0.7
12.8
15.3
15.5
15.4
20.9
14.3
15.7
13.4
14.9
15.6
13.6
14.0
14.0
14.1
13.8
15.1
13.7
14.0
14.2
15.2
0.3
0.4
0.4
0.3
0.5
0.3
0.4
0.4
0.4
0.4
0.3
0.3
0.3
0.3
0.3
0.3
0.3
0.3
0.3
0.3
2.3
2.9
2.7
2.6
3.8
2.5
2.9
2.5
2.9
2.9
2.5
2.6
2.6
2.7
2.6
2.7
2.7
2.7
2.8
2.6
100.9
96.0
115.6
115.2
104.1
115.7
105.5
71.6
102.3
70.8
101.1
106.0
110.5
115.9
106.6
119.9
110.6
114.1
125.5
119.0
2.3
2.9
2.8
2.8
2.7
2.6
2.6
3.5
2.7
10.5
2.3
2.4
2.4
2.4
2.3
2.5
2.3
2.4
2.4
2.7
23.4
25.6
24.3
23.7
33.4
23.0
27.4
25.3
25.0
26.6
23.1
22.9
22.4
22.0
23.2
23.6
23.2
22.6
23.5
23.2
2.2
2.5
2.4
2.3
3.3
2.2
2.6
2.4
2.4
2.6
2.2
2.2
2.2
2.2
2.3
2.3
2.3
2.3
2.4
2.3
82.7
87.3
120.1
94.9
94.2
100.1
95.5
63.9
122.4
62.8
82.1
88.1
89.8
88.8
85.5
94.5
89.2
91.0
95.5
98.1
133.2
187.9
143.9
138.4
291.0
126.9
170.9
224.7
164.6
268.0
152.5
152.5
143.1
131.7
143.6
126.3
150.7
144.2
130.0
125.3
0.27
0.26
0.37
0.34
0.32
0.43
0.31
0.16
0.31
0.18
0.31
0.31
0.32
0.29
0.26
0.32
0.29
0.26
0.26
0.44
221.2
220.5
219.8
220.3
219.8
220.0
220.3
222.6
221.0
223.3
220.7
221.1
220.9
221.7
220.8
221.5
220.5
220.8
220.0
220.0
MONSOON CONTROL OVER EROSION
Sample #
195
196
Table 5. Fission track analytical data for Holocene Indus delta sands
Sample no./ Strat age/ No. of
Field no.
lithology crystals
No apatite
Apatite
Apatite
Apatite
Apatite
Zircon
Apatite
44
15
16
70
28
61
rd
Nd
1.317
1.317
1.220
1.317
0.493
1.220
3651
3651
6107
3651
3450
6107
Spontaneous
rs
Ns
Induced
ri
Ni
0.101 135 5.538 6762
0.221
57 3.681
949
0.109
50 4.036 1857
0.162 661 4.122 16735
6.107 2404 5.414 2131
0.846 297 4.05 14219
Age
dispersion
Px2 RE%
0
3.0
5.3
0
0
0
Central
age (Ma)
+ 1s
1st age
comp.
2nd age
comp.
3rd age
comp.
4th age
comp.
124.5 4.4 + 1.0 2.6 + 0.3 (40)
9 + 3 (1)
24 + 4 (3)
56.7 11.1 + 2.7
7.4 + 1.7(13) 23 + 4 (2)
40.4 5.5 + 1.0 1.8 + 0.7 (6)
7.7 + 1.2 (10)
45.5 8.9 + 0.7 3.5 + 0.4 (20) 8.7 + 0.5 (50)
64.7 34.9 + 4.4 17.1 + 0.9 (14) 42.3 + 4.2 (9) 96 + 11 (4)
79.8 4.4 + 0.6 2.2 + 0.3 (40) 9.6 + 0.9 (21)
Note: (i) Track densities are (106 tr cm22) numbers of tracks counted (N) shown in brackets. Rd is the induced track density of the dosimeter. Nd is the number of tracks counted in the dosimeter/ Ns is
the number of spontaneous tracks counted in the sample. Ni is the number of induced tracks counted in the sample. (ii) Analyses by external detector method using 0.5 for the 4p/2p geometry correction
factor; (iii) Ages calculated using dosimeter glass CN-5; (apatite) zCN5 ¼338 + 4; CN-2 (zircon) zCN2 ¼127+4 calibrated by multiple analyses of IUGS apatite and zircon age standards (Hurford 1990);
(iv) Px2 is the probability of obtaining x2 value for v degrees of freedom, where v ¼ no. crystals – 1. RE %, age dispersion (or the spread of the individual crystal data) is given by the % relative standard
deviation of the central age; (v) Central age is a modal age, weighted for different precisions of individual crystals (Galbraith 1990).
P. D. CLIFT ET AL.
KB-34-4
KB-19-4
KB-23-3
KB-5-2
KB40-5
KB40-5
TH-10-8
Dosimeter
MONSOON CONTROL OVER EROSION
197
Table 6. Ar – Ar analytical data for detrital biotite grains extracted from Holocene Indus delta sands
KB-41-2
Age (Ma)
6.88
7.45
7.70
8.05
8.69
9.09
9.09
9.14
9.32
9.35
9.61
9.67
9.80
10.16
10.26
10.49
11.37
11.52
12.69
15.40
15.87
15.89
16.30
16.44
18.11
18.51
19.55
21.90
24.96
25.52
26.45
26.52
26.55
30.15
32.80
33.23
38.04
40.60
42.28
43.18
43.80
116.42
126.38
246.18
366.70
572.73
TH-4-6 Age
(Ma)
0.22
0.41
0.48
0.82
0.97
1.29
1.36
1.39
1.71
+2s
+1.64
+3.23
+0.44
+2.80
+0.66
+0.37
+0.21
+0.44
+0.18
+0.81
+3.81
+0.83
+0.39
+0.93
+3.69
+0.70
+0.65
+2.31
+1.71
+2.41
+0.79
+1.04
+0.87
+0.64
+0.51
+0.34
+0.74
+3.90
+1.98
+1.02
+1.48
+1.07
+0.54
+0.67
+0.55
+0.78
+1.14
+0.60
+1.07
+0.57
+0.39
+0.81
+0.93
+1.16
+1.99
+3.19
+2s
+1.07
+0.91
+0.55
+0.67
+1.13
+0.37
+0.46
+0.64
+0.75
40
Ar(r)
(%)
12.14
6.28
35.45
4.70
55.30
55.48
77.40
48.89
84.63
84.66
5.08
59.20
69.54
66.19
6.06
82.14
77.99
16.00
13.29
10.24
46.97
41.46
25.53
76.76
58.42
82.14
86.39
8.48
20.80
81.10
32.09
89.69
86.09
61.70
92.82
90.30
42.20
85.08
53.26
58.88
78.45
95.22
89.48
98.97
98.92
99.29
40
Ar(r)
(%)
8.34
9.58
5.14
13.40
13.22
46.53
22.69
28.52
20.85
39
Ar(k)
(%)
TH-4-6 Age
(Ma)
1.35
0.74
3.42
3.35
1.84
3.91
2.79
3.88
4.17
1.30
1.00
1.35
2.82
1.20
0.75
1.43
1.63
0.83
1.67
2.34
1.83
1.51
2.88
1.59
3.26
2.25
1.40
2.13
2.06
1.18
1.65
1.04
2.12
2.37
1.97
1.67
2.07
1.83
1.88
4.75
5.36
1.92
1.76
3.60
1.47
2.68
1.85
2.17
2.37
2.53
2.56
2.75
2.76
2.76
2.76
2.79
3.22
3.24
3.24
3.31
3.32
3.32
3.38
3.42
3.44
3.53
3.54
3.55
3.66
3.75
3.84
3.87
3.97
4.17
4.34
4.42
4.49
4.5
4.51
4.53
4.58
4.63
4.63
4.71
4.76
4.83
4.86
4.91
5.03
5.04
5.10
5.14
5.15
5.18
5.20
5.34
5.57
5.87
6.24
6.27
6.30
6.35
6.52
6.55
6.70
39
Ar(k)
(%)
0.25
0.29
0.56
0.43
0.22
0.66
0.87
0.43
0.37
+2s
+0.60
+0.94
+0.33
+0.54
+0.36
+0.56
+0.24
+0.63
+0.23
+0.75
+0.30
+0.79
+0.88
+0.64
+0.56
+0.52
+0.20
+0.84
+0.29
+0.69
+0.27
+0.59
+0.44
+0.56
+0.45
+0.37
+0.47
+0.45
+0.25
+0.67
+0.39
+0.50
+0.36
+0.49
+0.73
+0.53
+0.21
+0.38
+0.75
+0.55
+0.52
+0.39
+0.62
+0.16
+0.46
+0.63
+0.49
+0.46
+0.25
+0.16
+0.91
+0.71
+0.61
+0.36
+0.64
+0.51
+0.87
+0.38
+0.64
40
Ar(r)
(%)
43.17
28.16
30.64
62.68
14.67
14.63
43.69
23.42
55.22
46.23
36.46
33.64
38.98
44.40
57.69
63.30
45.33
56.01
21.48
50.22
32.29
10.88
41.60
70.46
41.70
52.81
36.91
50.52
56.30
58.55
27.75
44.28
44.04
43.77
39.79
13.16
55.84
47.08
59.64
64.99
42.41
56.64
45.98
49.53
52.18
70.39
52.18
49.86
43.90
71.14
48.50
57.39
55.76
58.96
65.04
50.78
54.76
55.42
65.22
39
Ar(k)
(%)
0.51
0.36
1.29
0.52
1.98
0.67
1.21
0.49
1.83
0.44
1.18
0.37
0.30
0.41
0.64
0.52
1.98
0.35
2.43
0.49
1.62
1.43
0.92
0.56
0.51
0.74
0.93
0.92
1.78
0.40
2.10
0.66
1.44
0.63
0.37
3.40
2.33
1.13
0.34
0.75
0.63
0.75
0.43
3.90
0.88
0.47
0.91
1.00
2.30
2.51
0.32
0.53
0.44
1.11
0.44
1.13
0.28
1.25
0.62
(Continued)
198
P. D. CLIFT ET AL.
Table 6. Continued
TH-4-6 Age
(Ma)
7.47
7.82
8.21
8.27
8.37
8.39
8.62
8.87
9.42
11.29
11.61
12.73
14.18
16.09
16.63
17.25
17.86
18.13
18.67
19.12
19.86
20.08
21.91
25.48
27.75
29.01
31.37
41.00
53.50
92.92
111.32
+2s
+0.69
+1.03
+0.59
+0.51
+0.69
+0.44
+0.47
+0.57
+0.17
+0.27
+0.30
+0.94
+0.21
+0.38
+0.34
+0.25
+0.80
+0.25
+0.54
+0.49
+0.57
+0.71
+0.32
+1.34
+0.25
+0.50
+0.45
+0.63
+0.71
+0.70
+0.62
40
Ar(r)
(%)
41.98
61.43
40.77
24.57
60.82
75.78
52.41
61.82
62.58
56.83
65.97
80.57
68.42
85.05
79.19
81.98
91.50
75.91
80.59
85.30
71.92
82.82
79.92
75.56
87.03
75.20
76.57
76.73
92.32
95.18
97.04
39
Ar(k)
(%)
0.62
0.25
0.62
2.36
0.61
0.58
0.92
0.42
2.73
2.71
0.97
0.27
3.69
1.36
1.26
1.60
0.31
2.37
0.58
0.84
0.49
0.41
1.36
0.23
1.94
1.16
1.12
0.82
0.64
0.57
1.26
Canberra, using Excimer Laser Ablation Inductively Coupled Plasma Mass Spectrometry
(ELA-ICP-MS) employing a pulsed 193 mm ArF
LambdaPhysik LPX 1201 UV Excimer laser and
an Agilent 7500 quadrupole ICP-MS. The zircons
were separated from the bulk sediment by conventional magnetic and heavy liquid separation techniques. In this study we analysed two samples
(Jati-16-1 and KB-34-1), which were not considered
by the earlier study of Clift et al. (2008). The
extracted zircons were mounted in epoxy resin and
polished. Dating by ELA-ICP-MS followed the procedure described in Campbell et al. (2005). Our
method employs standard zircon TEMORA2 and
NIST610 silicate glass (Pearce et al. 1997; Black
et al. 2004) where the latter is used for concentration
information and for U/Th determination. As we
cannot measure common Pb (204Pb) directly
because of systemic Hg, we use a 208Pb-based correction only when that correction makes the analysis
more concordant than the uncorrected version. Once
the data were compiled, an analysis was rejected for
interpretation on the basis of the following: (a) the
observed variance on 206Pb/238U or 207Pb/206Pb
(depending if the grain is . or ,1200 Ma) is
more than three times that calculated from counting
statistics (this procedure omits grains that record
mixed ages), or (b) the grain is deemed to be discordant. Analysis time drift corrections were applied to
both analytical sessions. Results of the U – Pb dating
are shown in the supplementary material. Overall
uncertainty on an individual measurement is about
1–2%.
Results
Mineralogy
Detrital modes in the Indus Holocene sands are
typical of sediments derived from collision
orogens (Garzanti & Andò 2007), with medium
quartz content and equally abundant feldspars and
lithic grains (quartz 49 + 4%, feldspar 26 + 3%,
lithics 25 + 3%). Using a Dickinson ternary
diagram (Fig. 3a) the sands mostly plot within
the ‘recycled orogen’ field, with minor overlap in
the ‘dissected arc’ range. In this respect they are
similar to sandstones found in the Himalayan
foreland basin, at least since the start of the
Neogene (Najman & Garzanti 2000). Lithic grains
comprise equally abundant sedimentary (limestone,
dolostone, siltstone) and metamorphic types.
However, volcanic, metavolcanic, and metabasite
lithic grains are very minor, but decrease up-section
in the lower part of the core (120 –60 m depth,
20 –9.5 ka; Fig. 4), with the greatest change
between 12.2 and 10.6 ka. This trend suggests
upward-decreasing relative contributions from
Kohistan-like Transhimalayan sources and/or the
West Pakistan ophiolites. The composition of the
lithic grains defines the sands as typical of ‘suture
belts’ in the ternary diagram (Fig. 3b). Conversely,
carbonate grains, which are almost absent at the
base of the Keti Bandar section (LGM) increase in
the uppermost 90 m (since c. 12 ka), suggesting
increasing contributions from sedimentary to metasedimentary strata and/or more arid climatic conditions that do not favour dissolution of these grains.
The total heavy-mineral content is remarkably
constant (4.2 + 0.7%) in the six very fine-grained
sands analysed (KB-5-2, TH-10-8, KB-20-1,
KB-34-4, KB-40-5, and KB-41-2), indicating that
intrastratal solution is negligible throughout the
cored sections. Heavy minerals are less abundant
in the analysed 63 –250 mm fraction of the other
three silt-sized samples (KB-23-2, KB-26-2, and
KB-30-4), but this does not mean that bulk
samples contain fewer heavy minerals, because
denser detrital grains are markedly concentrated in
the fine tail of the size distribution of each sample
MONSOON CONTROL OVER EROSION
(a)
Tra
ns.
co
nti
ne
nt
Q
Ba
se
me
nt
up
lift
Recycled
Orogen
Dissected arc
Transitional arc
Undissected arc
F
L
(b)
199
(ZTR) 3 + 1% and all other heavy minerals
6 + 2%) (Garzanti et al. 2005). Slightly higher
garnet content in modern bedload sand is ascribed
to the selective entrainment of less dense grains
and enrichment in denser grains in lag deposits on
the channel bottom (Slingerland 1984). Most
remarkable is the virtual lack of limestone grains
and of pyroxene at the bottom of the Keti Bandar
core (117–120 m depth; i.e. deposited at the
LGM), which would indicate strong chemical
weathering. This observation may be linked to a
humid climate at the LGM, for which there is no
evidence, or alternatively and more likely, due to
prolonged exposure prior to the Holocene
transgression.
Lm
Sr isotope evolution
Suture belts
Mixed arc and
subduction complex
Magmatic arc
Lv
Ls
Fig. 3. (a) Triangular QFL plot (Q, quartz, L, lithics, F,
feldspar) and (b) Lm (lithic metamorphic), Lv (lithic
volcanic) Ls (lithic sedimentary) plots, with fields from
Dickinson (1985) for the Indus Holocene sands.
because of settling-equivalence effects (Garzanti
et al. 2009). Amphiboles (mainly blue-green hornblende, comprising 52 + 5% of the total heavy
mineral population) prevail over epidote
(27 + 4%), subordinate garnet (6 + 4%) and clinopyroxene (6 + 3%), and minor tourmaline, titanite,
hypersthene, kyanite, sillimanite, rutile, staurolite,
chloritoid and zircon in order of decreasing abundance (5 + 3%). Hypersthene increases slightly
up-section, suggesting increasing contribution
from the Kohistan Arc in the upper part of the
core (depth ,60 m; since c. 9 ka), since this
mineral is distinctive of erosion from arc units
(Cerveny et al. 1989).
Marked temporal changes in mineralogy are not
apparent (Fig. 4), and sediment composition
remains comparable to the modern Indus detrital
modes (quartz 48 + 4%, feldspar 21 + 3%, lithics
32 + 5%) and heavy-mineral assemblages (amphibole 50 + 8%, epidote 25 + 7%, garnet 12 + 3%,
pyroxene 4 + 3%, zircon þ tourmaline þ rutile
Temporal evolution in Sr isotopes is shown together
with changing Nd isotopes in Figure 5. What is
apparent is that the two systems are closely correlated and that Sr increases rapidly from low values
at the LGM and until c. 13 ka, after which there is
a rapid rise to a high 87Sr/86Sr between 8 and
9 ka. Subsequently, 87Sr/86Sr values decrease
slightly to the present day. The correlation suggests
that Sr isotope composition is dominated by source
and provenance rather than by chemical weathering
intensity, although the total number of analyses
is rather low. As with the Nd data there is no clear
correlation between isotopic composition and
grain size. Sediments of the same grain size show
a variety of isotopic ratios (Fig. 5). The shift to
higher isotope ratios is consistent with increased
relative erosion from the radiogenic crust of the
Lesser and Greater Himalaya, and away from the
more primitive crust of Kohistan and the Transhimalaya (Trivedi et al. 1984; France-Lanord &
Le Fort 1988; Scaillet et al. 1990; Ahmad et al.
2000). Because the change in isotope character
occurs at a time of greatly increased sediment flux
to the delta we rule out the possibility that the
change in isotope character reflects decreased sediment flux from the arc sources lying north of the
Himalayan ranges and in any case the increase in
hypersthenes (but not metabasic rocks) up-section
suggests more erosion from Kohistan, not less.
However, the trend in the Nd isotope curve indicates
that the influence of Kohistan on the total sediment
composition is swamped by increased flux from
Himalayan sources.
Organic carbon
Although the shift to higher 87Sr/86Sr values in the
Early Holocene cannot be interpreted as indicating
stronger chemical weathering under the influence
of a stronger summer monsoon, organic carbon
200
P. D. CLIFT ET AL.
Proportion of total
mineralogy (%)
(a)
Age (ka)
0
10
20
30
40
Proportion of heavy mineral
population (%)
(b)
50
0
60
0
0
5
5
10
10
15
15
20
20
Quartz
Feldspar
Sedimentary lithic grains
Metamorphic lithic grains
Igneous lithic grains
10
20
30
40
50
Amphibole Group
Pyroxene Group
Epidote Group
Zircon, tourmaline,Ti-oxides,
titanite, apatite,monazite
Chloritoid, staurolite, andalusite,
kyanite, sillimanite
Garnet
Fig. 4. Plots showing the evolution in sand mineralogy at the Keti Bandar borehole since 20 ka. (a) Major mineral
groups, and (b) only heavy minerals. Data are plotted from Tables 1 and 2. The plots confirm the overall lack of strong
changes in mineralogy throughout the deglaciation process.
analysis can be used to constrain environmental
conditions. Total organic carbon (TOC) concentrations are low and range between 0.16% and
0.44% (Table 4), consistent with the generally arid
conditions in the Indus basin. There is no obvious
TOC variation with age of sedimentation and most
of the samples remain in a narrow range around
0.3% (Fig. 6a). Bulk organic carbon d13C varies
between – 23.3‰ and –19.7‰, but only two
samples with very low TOC (0.16% and 0.18%)
have d13C lower than –21.7‰ (Fig. 6b). These
negative d13C values ( –22.6 and –23.3‰) are
associated with the lowest TOC and correspond to
sandy sediments, as indicated by low Al/Si ratios.
In these two quartz-rich sands, rock-derived
organic carbon is likely to be a major component
of the total organic carbon content (Galy et al.
2008). Their stable isotopic composition is therefore
not representative of modern organic carbon
directly derived from the biosphere. Excluding
these two samples, d13C shows a c. 2‰ variation
around an average value of –20.6‰. In detail,
MONSOON CONTROL OVER EROSION
201
Fig. 5. Diagram showing the variability in bulk sedimentary Nd and Sr isotope character since the Last Glacial
Maximum. Sediments are from the Indus delta and the Indus Canyon. Letters indicate grain size of sediment: C, clay; SI,
silt; FS, fine sand; S, sand. Black arrows indicating age control points and Nd data are from Clift et al. (2008). Sr data
are from Table 3.
d13C reaches a minimum after the LGM and likely
until the Younger Dryas. d13C increases between
12 ka and 5 ka and finally decreases again up to
present (Fig. 6b).
Organic carbon (OC) can be derived from a
mixture of different sources: terrestrial OC derived
from vegetation, soils and autotrophic production
in the river and marine organic carbon. Historically,
the Indus River is characterized by high sediment
concentration, which limits autotrophic productivity
(Ittekkot & Arain 1986). Terrestrial inputs may
therefore be derived from the vegetation present in
the basin, either directly (plant debris) or indirectly
(soil organic carbon). C3 plants have a considerable
range in d13C. Arid ecosystems are enriched in 13C
(as high as 222‰) (Farquhar et al. 1989), but
closed canopy flora are depleted in 13C, with d13C
values as low as 235‰ (van der Merwe & Medina
1989). However, the average C3 value is about
– 26‰. In contrast, C4 plants have a much more
202
P. D. CLIFT ET AL.
(a)
(b)
Total Organic Carbon (%)
0.15
0.25
0.35
–23
0
5
5
10
10
–22
–21
–20
Age (ka)
0
d13C (‰)
15
15
LGM
LGM
Fig. 6. Diagrams showing (a) the evolution in total organic carbon (TOC) and (b) carbon isotope character of bulk
sediments from the Indus delta. See Table 4. TOC values are generally small and show little variation with time. Lowest
TOC values correspond to negative d13C values associated with reworking of old organic matter. The 2‰ positive shift
between 12 ka and 5 ka is significant and may be related to an increase of C4 plants input. See Table 4 for data.
restricted d13C range, with an average d13C value
around –13‰ (Deines 1980; Hattersley 1982; Collister et al. 1994). In the Arabian Sea, modern marine
plankton has d13C values around –20‰ (Fontugne
& Duplessy 1978) and its isotopic composition has
likely remained fairly stable during the last 20 ka.
The sedimentological study of this record clearly
indicates a marine transgression during the Holocene. Therefore, the middle section of the record
at Keti Bandar (15 –70 m) may have been influenced by marine organic carbon, whereas it might
be expected to be negligible in the upper and
lower sections.
In these two terrestrial sections of the record,
bulk organic carbon d13C indicates mixed C3/C4
vegetation in the Indus basin. The lowest part of
the record (LGM to 12 ka) shows a slight decrease
of the bulk organic carbon d13C from –20‰ to
–21‰. This shift may be related to an increase of
the C3 plants proportion in the basin during the
time of deglaciation. The c. 2‰ positive shift
between 12.9 ka and 4.1 ka probably reflects
increasing contribution of marine OC, although it
might also indicate an increase in the proportion
of C4 plants in the basin. Conversely, the reversed
trend from 4.1 ka to present likely reflects decreasing contribution of marine organic carbon, or an
increase of the C3 plants proportion in the basin.
Comparison with published organic carbon data
from the Bengal Fan system indicates that the Indus
is relatively low in TOC (Galy et al. 2007b).
Maximum values range up to 0.44% compared to
.1.1%. However, like the Bengal sediment our
data show a rough first order correlation between
Al/Si ratios and TOC (Fig. 7). This is consistent
with a control of the organic carbon content by the
sediment properties, specifically a preferential
association of organic carbon with fine grain sediments enriched in phyllosilicates (clays and micas)
(Galy et al. 2008). Figure 7 shows that the slope
on the TOC v. Al/Si chart, which characterize the
organic carbon loading, is lower in the Indus basin
than in the Bengal Fan, reflecting its more arid
environmental conditions.
MONSOON CONTROL OVER EROSION
although with only 19 grains this sample may not
be representative (Clift et al. 2004). The Greater
and Lesser Himalaya, together with the Karakoram
have yielded abundant young AFT ages that would
be consistent with a source in those ranges. The
slightly older ages seen in the reworked Miocene
foreland sedimentary rocks of the Siwaliks argues
against them being important since 8.7 ka, although
they may partly be responsible for the older age
population seen at the LGM. Other possible
sources for the older grains deposited at the
LGM are the Transhimalaya or Kohistan. Further
source characterization is possible using Ar –Ar
and U – Pb methods.
al Fan
0.35
Beng
elt
a
0.25
Ind
us
D
TOC (%)
0.30
0.20
0.15
0.00
0.10
0.20
0.30
203
0.40
0.50
Al/Si
Fig. 7. Diagram showing the relationships between mud
Al/Si and TOC for the Indus Holocene. Trend shows
much lower slope than that recognized for the Bengal
Fan (Galy et al. 2007b), suggesting much lower organic
productivity.
Fission track analyses
The results of the fission track analyses are shown
graphically in Figure 8 in the form of radial plots
that show the ages and uncertainties of single
grain apatite and zircon grains (Galbraith 1990).
Statistical analysis allows a central age to be
assigned for each sample, with greater confidence
for those samples with more abundant grains. In a
complex system like the Indus 100 grains are
needed for a robust result (Ruhl & Hodges 2005)
and in several of these sands the numbers are so
low that they are not useful. Three samples can be
used to look at the general development in sediment
source since the LGM. Sample KB-40-5 has a
central age of 9.0 + 1 Ma, yet by 8.7 ka sample
KB-19-4 shows a central age of only 4.4 + 1 Ma.
A similar age is yielded by sample TH-10-8,
deposited around 7 ka. The radial plots show that
there is a minority population dating .10 Ma, but
that in the younger sands in particular this is very
minor.
The change in apatite fission track (AFT) ages
during the Holocene must reflect a change in provenance as the duration is not long enough for this to
represent a change in source exhumation rates.
Comparison of the age spectrum in the sediments
with AFT ages from possible source terrains
allows the changing erosion patterns to be constrained (Fig. 9). Probability density diagrams
emphasize the young AFT ages of the younger sediment and show the ‘tail’ of grains older than 10 Ma
seen in the LGM sediment but not since that time.
Comparison with the modern Indus sediments
shows a similar pattern to the recent sediments,
Mica ages
Ar –Ar cooling ages in biotite and muscovite micas
document the age that these grains cooled below
c. 280 8C and 350 8C respectively (Hodges 2003).
As exhumation is diachronous across the Himalaya
these ages can be used as powerful provenance tools
in modern and ancient South Asian sediment (White
et al. 2002; Clift et al. 2004). Figure 10 shows the
range of biotite cooling ages for two core samples
and one modern river sand sample. The age
spectra for the modern and 6.4 ka sand differ in
one key aspect from the LGM sand at Keti
Bandar, in the abundance of grains ,10 Ma. All
samples show minority populations with older,
albeit Cenozoic cooling ages, At the LGM, the
most common age lies around 9 Ma, compared to
c. 4 Ma for the younger sediments. Comparison
with the rather limited number of bedrock analyses
suggests that the Karakoram makes a relatively
good match as a possible source at the LGM,
although there are no published data for the Transhimalaya or Lesser Himalaya. Cooling ages in the
Greater Himalaya largely range 10–24 Ma and do
not account for the up-surge of young ages in
the Holocene delta, although there is a significant
population of 10–14 Ma grains in the modern
river that may be derived from this area. Nanga
Parbat is a possible source of the 1– 7 Ma grains
seen in both younger samples.
Additional source constraints are possible using
the muscovite Ar –Ar ages reported by Clift et al.
(2008). This system has the advantage over biotite
in being more widely measured in the potential
source regions. Figure 11 shows that like the
biotite data the 6.4 ka and modern sediments have
several muscovite grains dating ,10 Ma, which
the LGM sediment does not contain. A probability
maximum around 18 Ma at 6.4 ka and at the LGM
correlates with known sources in the Lesser and
Greater Himalaya, although there is some overlap
between these sources that makes their separation
hard with this method. However, we note that
204
P. D. CLIFT ET AL.
40
KB-40-5 (Apatite), >20 ka, LGM
Central Age: 9±1 Ma
P(X2): 0.0%
Relative Error: 46%
Number of grains: 70
KB-40-5 (Zircon), >20 ka, LGM
Central Age: 35±4 Ma
P(X2): 0.0%
Relative Error: 65%
Number of grains: 28
30
20
+2
200
150
100
10
0
-2
5
50
+2
0
-2
% relative error
1
% relative error
70
0
28
7
0
10
20
30
40
50
10
60
10
12
20
30
Precision (1/sigma)
Precision (1/sigma)
KB-5-2 (Apatite), 210 a depositional age
Central Age: 6±1 Ma
P(X2): 5%
Relative Error: 40%
Number of grains: 16
20
16
12
+2
8
0
6
40
30
KB-19-4 (Apatite), 8.7 Ka depositional age
Central Age: 4.4±1 Ma
P(X2): 0.0%
Relative Error: 124%
Number of grains: 44
20
10
+2
5
0
-2
1
-2
1
% relative error
55
0
10
20
% relative error
89
11
0
30
10
20
30
8
40
50
Precision (1/sigma)
Precision (1/sigma)
KB-23-3 (Apatite), 9.3 ka depositional age
Central Age: 11±3 Ma
P(X2): 3%
Relative Error: 57%
Number of grains: 16
40
30
20
16
TH-10-8 (Apatite), 7.0 ka depositional age
Central Age: 4.4±1 Ma
P(X2): 0.0%
Relative Error: 80%
Number of grains: 61
12
8
20
+2
5
+2
0
10
-2
5
0
-2
1
% relative error
76
1
13
0
10
20
30
Precision (1/sigma)
% relative error
63
6
0
10
20
30
40
50
60
Precision (1/sigma)
Fig. 8. Radial plots (Galbraith 1990) showing the ages and uncertainties of single grain apatite and zircon grains within
Holocene sands from the Indus delta. Locations of samples are shown in Figures 1 and 2.
Greater Himalayan muscovite ages peaks around
20 Ma, whereas the limited data from the Lesser
Himalaya peak around 16 –18 Ma. The greatest
probability peak in the detrital grains is younger
than 20 Ma, consistent with the Lesser Himalaya
being the dominant source. Again the muscovite
confirms that the Siwaliks are not dominant sediment sources because the cooling ages are generally
MONSOON CONTROL OVER EROSION
205
Fig. 9. Probability density plots showing the range of apatite fission track central ages for the sediment samples
analysed versus the ages found in a variety of possible source terrains. Siwalik data is from Van der Beek et al. (2006).
Karakoram data is from Zeitler (1985), Poupeau et al. (1991) and Foster et al. (1994). Greater Himalayan data are from
Kumar et al. (1995), Sorkhabi et al. (1996), Searle et al. (1999), Jain et al. (2000), Thiede et al. (2004) and Bojar et al.
(2005). Lesser Himalayan data are from Vannay et al. (2004) and Thiede et al. (2004). Pakistan Himalayan data are from
Zeitler (1985). Transhimalayan data are from Zeitler (1985), Zeilinger et al. (2001), Clift et al. (2002a) and Kirstein
et al. (2006). Figure shows preference to younger grain ages with the onset of the Holocene, consistent with relatively
more erosion from the Greater and Lesser Himalaya and less from the Siwaliks and Transhimalaya. See Table 5 for data.
too young. As for the ,10 Ma muscovite grains
bedrock data suggest either Nanga Parbat or the
Lesser Himalaya as likely sources. A probability
maximum at 15 –16 Ma in the modern river
matches several known sources in the Lesser
Himalaya but not Nanga Parbat. This population is
less abundant in the 6.4 ka sample. We conclude
that the mica dating argues for reduced erosion in
the Karakoram and more erosion in the Lesser
Himalaya or Nanga Parbat between the LGM and
the Early Holocene. As these sources are both negative in 1Nd (Parrish & Hodges 1996; Whittington
et al. 1999; Ahmad et al. 2000) increased relative
flux in either could explain the observed bulk sediment Nd and Sr isotope evolution (Fig. 5).
Zircon dating
Zircon U –Pb dating has proven an effective provenance tool in South Asia because it preserves the
original age of crystallization of the source rocks,
which varies significantly across the Himalayas
and into Tibet (DeCelles et al. 2000). In this study
we augment the data presented by Clift et al.
(2008) with two additional samples in order to
define the Holocene provenance evolution better.
Figure 12 shows the age spectra for the four core
samples, plus modern river data compared with
various source terrains. All the sediments show a
large population with grains of ,150 Ma and a
spread of other older grains. Some samples show
particularly well developed groups. The LGM
sands show many grains dated at 800–1100 Ma,
reducing in number up-section. The modern river
sand shows an especially large number of grains
c. 1800 Ma compared to the older sediments.
The new data are consistent with the older in
suggesting significant erosion from the Karakoram,
or the Transhimalaya, especially at the LGM. In
addition, the zircon indicate increased erosion
from the Lesser Himalaya going up section. Very
few of the grains are young enough to match those
measured from the Nanga Parbat gneiss. This
resolves one of the ambiguities from the mica
Ar –Ar data in separating the erosional flux from
the Lesser Himalaya. Despite its dramatic exhumation history (Zeitler et al. 1993) it appears that
Nanga Parbat is a modest contributor of sediment
to the Indus.
The provenance can be further quantifying by
dividing up the detrital zircons into families. We
choose 0–20 Ma grains to represent the flux from
Nanga Parbat, 20 –55 Ma grains are rarely known
outside the Karakoram Batholith. The range
55 –300 Ma is chosen as a suitable range for much
of the activity in Kohistan and the Transhimalaya,
206
P. D. CLIFT ET AL.
Greater Himalaya
Nanga Parbat
Karakoram
0
10
20
30
40
50
60
Modern Indus at Thatta
N = 95
0
10
20
30
40
50
60
TH-4-6, Biotite, <6.4 ka
N= 46
0
10
20
30
40
50
60
KB-41-2, Biotite, 25 ka
N = 99
0
10
20
30
40
50
60
Age (Ma)
Fig. 10. Probability density plots showing the range of Ar–Ar cooling ages in biotite grains from three sand samples
from the Indus delta. Top section shows known range of possible source ages from the Greater Himalaya (Copeland
et al. 1990; Searle et al. 1992; Metcalfe 1993; Inger 1998; Stüwe & Foster 2001; Godin et al. 2006; Wang et al. 2006),
Nanga Parbat (Zeitler et al. 1989; Winslow et al. 1996; Treloar et al. 2000) and Karakoram (Searle et al. 1989;
Brookfield & Reynolds 1990; Krol et al. 1996; Villa et al. 1996). See Table 6 for data.
300– 1400 Ma grains represent the Greater
Himalaya and those older than 1400 Ma the Lesser
Himalaya. Because of overlaps in age ranges such
a budget is necessarily schematic but does show
the general trends in provenance evolution
because the different ranges have preferred ages
that are typical if not unique to them. In Figure 13
we plot pie charts to show how the bulk composition
MONSOON CONTROL OVER EROSION
207
Greater Himalaya
Probability
Nanga Parbat
Siwaliks
Lesser Himalaya
Modern River at Thatta (48 grains)
Probability
0-10 Ma (N. Parb.+L. Him.) = 15%
10-40 Ma (L.+Gr.. Him.) = 80%
>40 Ma (Transhimalaya) = 4%
TH-4-6, Muscovite, <6.4 ka (99 grains)
Probability
0-10 Ma (N. Parb.+L. Him.) = 25%
10-40 Ma (L.+Gr. Him.) = 70%
>40 Ma (Transhimalaya) = 5%
KB-41-2, Muscovite, >20 ka (50 grains)
Probability
0-10 Ma (N. Parb.+L. Him.) = 4%
10-40 Ma (L.+Gr. Him.) = 84%
>40 Ma (Transhimalaya) = 12%
0
10
20
30
40
Age (Ma)
Fig. 11. Probability density plots showing the range of Ar–Ar cooling ages in muscovite grains in the glacial sample,
at ,6.4 ka and in the modern river (2004), compared to those in possible source regions. Top section shows the
known range of possible source ages from the Greater Himalaya within the Indus basin (Searle et al. 1992; Metcalfe
1993; Inger 1998; Walker et al. 1999, Stephenson et al. 2001), Lesser Himalaya (Catlos et al. 2001; Bollinger et al.
2004; Vannay et al. 2004), Nanga Parbat (Smith et al. 1992; George et al. 1995; Treloar et al. 2000), and Siwaliks
(White et al. 2002; Szulc et al. 2006). Reprinted with permission from the Geological Society of America.
of the Indus sediments has changed from the LGM
to the present day. Again the heavy influence of
the Lesser Himalaya on the modern river is clear
and contrasts even with the mid Holocene
samples. Because of damming of the modern
Indus, most notably at Tarbela (Fig. 1), some of
the anomaly in the modern sample may be anthropogenic, although dams do exist on many of the Himalaya tributaries too (e.g. the Mangla Dam on the
Jhelum). All samples show very little sediment
from Nanga Parbat sources, but a consistent dominant flux from the Greater Himalaya.
208
P. D. CLIFT ET AL.
Nanga Parbat
Karakoram
Lesser Himalaya
Probability
Greater Himalaya
Siwaliks
Probability
Thatta, Modern Indus (130 grains)
2% Nanga Parbat
19% Karakoram+Transhim.
38% Greater Himalaya.
41% Lesser Himalaya
Probability
TH-10-1, Age = 7.0 ka (186 grains)
0% Nanga Parbat
28% Karakoram+Transhim.
38% Greater Himalaya.
34% Lesser Himalaya
Jati-16-1, Age = 8.0 ka (74 grains)
Probability
3% Nanga Parbat
44% Karakoram+Transhim.
31% Greater Himalaya.
22% Lesser Himalaya
Probability
KB-34-1, Age = 12.6 ka (117 grains)
2% Nanga Parbat
41% Karakoram+Transhim.
35% Greater Himalaya.
22% Lesser Himalaya
Probability
KB-40-1 and -41-2, Age > 20 ka (271 grains)
1% Nanga Parbat
40% Karakoram+Transhim.
42% Greater Himalaya.
16% Lesser Himalaya
0
1000
2000
3000
Age (Ma)
Fig. 12. Probability density plots showing the range of U– Pb ages in detrital zircons compared with source terrain
values. Top section shows known range of possible source ages from the Greater Himalaya (Gehrels et al. 2006),
Karakoram (Le Fort et al. 1983; Parrish & Tirrul 1989; Schärer et al. 1990; Fraser et al. 2001; Heuberger et al. 2007),
Lesser Himalaya (Parrish & Hodges 1996; DeCelles et al. 2000; Chambers et al. 2008), Nanga Parbat (Zeitler &
Chamberlain 1991; Zeitler et al. 1993), and the Siwaliks (DeCelles et al. 2000; Bernet et al. 2006). See supplementary
material for data.
MONSOON CONTROL OVER EROSION
209
Fig. 13. Pie diagrams showing the changes in the relative proportions of different zircon U –Pb age populations in sands
from the Indus delta. See Figures 1 and 2 for sample locations. Population 0 –20 Ma is a proxy for flux from Nanga
Parbat, whereas the 20– 55 Ma are likely from the Karakoram Batholith. 55– 300 Ma grains are dominantly from the
Transhimalaya (Ladakh and Kohistan batholith). Grains dated 300–1400 Ma are typical of sources in the Greater
Himalaya, while older grains are likely derived (directly or indirectly) from the Lesser Himalaya.
210
P. D. CLIFT ET AL.
Table 7. Predicted percentages of eroded material from a variety of western Himalayan source in five Indus
River sands spanning the LGM to present. The mean 1Nd values for each of the sources is a modal number
derived from published Nd isotope measurements from the bedrock
Source
1Nd
KB-40-1
KB-34-4
Jati-16
TH-10-8
TH-1
Depositional age (ka)
Nanga Parbat %
Karakoram and Transhimalaya %
High Himalaya %
Lesser Himalaya %
225
þ1
216
224
20
1
40
42
17
13
3
39
36
22
8
3
44
31
22
7
2
37
39
22
0
2
22
36
40
210.7
210.8
211.4
211.8
210.5
n/a
211.7
212.9
215.7
215.4
Predicted 1Nd
Observed 1Nd
Source: Nanga Parbat data is from Clift et al. (2002b) and Whittington et al. (1999), Greater Himalaya data is from Ahmad et al. (2000),
Deniel et al. (1987), Stern et al. (1989), France-Lanord et al. (1993), Parrish & Hodges (1996), Searle et al. (1997), Harrison et al. (1999),
Whittington et al. (1999). Lesser Himalaya data is from Ahmad et al. (2000) and Parrish & Hodges (1996). Transhimalayan data is from
Khan et al. (1997), Clift et al. (2000). Karakoram data is from Clift et al. (2002b) and Schärer et al. (1990).
Monsoon and erosion patterns
The different provenance proxies can be combined
to generate a ‘best-fit’ sediment budget for the Indus
since the LGM. Because of the large number of
grains and samples and the good degree of separation between sources we choose to base the
budget on the U –Pb zircon grains (Fig. 13), but
then cross-check this by calculating what the Nd
isotope composition of such a sediment mixture
would be given the known range of Nd isotope
characteristics in the sources. These predicted 1Nd
values can then be compared with the actual
measured values of these sediments (Clift et al.
2008). Because the Nd analyses are bulk analyses
they would be expected to yield good averages of
the sediment flux. In practice there are some significant departures between predicted and observed
1Nd values. This may reflect use of an inappropriate
1Nd value for the sources, yet we consider this unlikely because the modal values often lie close to
measured values from the major modern rivers,
which themselves should sample and average wide
areas of the possible sources (Clift et al. 2002b).
Alternatively, we suggest that the zircons, which
are interpreted simply in the pie diagrams of
Figure 13 are not as accurate as might be hoped in
characterizing the total mass flux because of age
overlap between the populations and sources.
There exists a further possibility that there is shortterm variability in the sediment provenance that
results in measurable differences in zircon populations for sediments that were deposited close
together in time.
In Table 7 we show a proposed erosion budget
for the Indus based on five sand samples. We use
the zircon populations shown in Figure 13 as a
starting model for estimating the flux from each of
the major sediment sources, but we adjust the relative proportions from each source to provide a
closer match with the measured 1Nd values.
Because the flux from the Karakoram and the Transhimalaya are hard to resolve from one another we
plot these together as a single source. In each case
the percentage adjustment from the observed was
not more than 3%, and usually +2% or less.
Figure 14 shows how this synthesized mass flux
varies with time. The evolutionary patterns defined
by this synthesis budget reflect many of the trends
seen in the single mineral plots. Greater Himalayan
flux remains high, if slightly variable throughout the
period, as might be expected. Erosion from Nanga
Parbat and the Lesser Himalaya because stronger
Nanga Parbat
Karakoram and
Transhimalaya
Proportion of total sediment (%)
Discussion
Greater Himalaya
Lesser Himalaya
50
40
30
20
10
0
0
5
10
15
20
Age (ka)
Fig. 14. Plot showing the evolving flux in zircon
populations during the Holocene. We highlight the fall in
relative flux from the Karakoram and Transhimalaya,
compared to a sharp rise in the Lesser Himalaya,
especially since 8 ka.
MONSOON CONTROL OVER EROSION
after the LGM, with a further sharp rise between
7 ka and the present day. At the same time flux
from the Karakoram and Transhimalaya suffered a
major decline. These changes may in part be
related to the damming of the trunk river at
Tarbela, which would raise the relative flux from
the eastern tributaries draining the Himalaya,
although these too have been dammed. Nonetheless,
this theory does not explain the shift to similar negative 1Nd values in the Early Holocene. In this case
we infer a similar shift to greatly enhanced erosion
of the Lesser Himalaya relative to the Karakoram,
peaking around 9 ka. The Nd isotopes suggest a
moderate fall in Lesser Himalayan erosion after
that time and before the most recent increase in
the past 250 years. The later change in zircon
sources (after 7 ka) compared to the earlier
changes in Nd isotopes (10–14 ka) may also
reflect a real lag in the sediment transport process
for the zircon crystals versus clay minerals.
The large scale changes in provenance tracked
by the Nd isotopes (Figs 5 and 15) reflect a shift
from preferential erosion of terrains lying to the
north, around the Indus Suture Zone at the LGM
to more erosion of the frontal Lesser Himalayan
ranges in the south by the early Holocene. We do
not think that drainage reorganization is responsible
for the changing sediment compositions, even
though this process has been used to explain
changes in Nd isotopes after around 5 Ma (Clift &
Blusztajn 2005). However, in this case the shift to
more negative 1Nd values between 12 and 8 ka
would require gain of isotopically negative
sources. The increase in sediment flux at that time
rules out loss of sources with positive 1Nd values
as an alternative explanation. There is no evidence
that the Punjabi tributaries, the Ravi, Jellum,
Chenab and Sutlej, were captured into the Indus as
recently as this time. Indeed, studies of Holocene
drainage on the eastern edge of the Indus catchment
indicate loss of drainage from Himalayan sources
(Ghose et al. 1979) since the LGM, which would
drive the opposite provenance shift than that
observed. We conclude that the changes are driven
by changing rates of sediment supply, not the
wholesale capture of the Punjabi tributaries.
When we compare the observed change in erosional style with records of the SW monsoon then
we see that intensification of the summer rains
[as tracked by speleothems (Fleitmann et al.
2003; Sinha et al. 2005) and pollen assemblages
(Herzschuh 2006)] correlates with the strong
change in Sr and Nd between 12 and 9 ka. This is
also the time of accelerated sediment flux to the
delta. Because the sediment composition changes
quickly and is quite different from the sand deposited at the LGM we can rule out the sedimentation
pulse as being caused by enhanced transport of
211
older glacially eroded sediment under the influence
of the strong Early Holocene monsoon. In any case
the Lesser Himalaya were not glaciated during the
LGM (Owen & Benn 2005) and so the deglaciation
process should not have directly affected the
erosion of these ranges. Instead the stronger
monsoon appears to be generating new sediment
by erosion under its precipitation maximum. Satellite data shows that precipitation maxima in the
western Himalaya are focused over the topographic
breaks in the Lesser and Greater Himalaya (Bookhagen & Burbank 2006) and that the change in provenance was probably caused by a strengthening of
rain and erosion in those zones. Studies of landslides
in the western Himalayan confirms that the Early
Holocene was a period of significant mass wasting
and thus sediment production within the Himalaya
(Bookhagen et al. 2005). In contrast, erosion in
the Karakoram appears to be largely glacially
driven and would have been strong at the LGM, as
well as today. Because the Karakoram lie in the
rain shadow of the Himalaya and derive most of
their water via the westerly jet (Karim & Veizer
2002) their erosion would not change significantly
as the summer monsoon intensified.
Tectonics and the monsoon
The primary conclusion of this study is that patterns
of erosion across the western Himalaya changed
significantly since 20 ka, driven by changes in
summer monsoon intensity. Controls on erosion
are important when considering the tectonic evolution of the Greater Himalaya because focused
erosion is considered to have been a key factor in
allowing deep buried metamorphic rocks to be
exposed at the surface. This is true whether channelflow (Beaumont et al. 2001; Hodges et al. 2001) or
orogenic wedge models are employed (Hilley &
Strecker 2004) to explain the origin of the Greater
Himalaya. Although we recognize that exhumation
of ultra-high pressures, such as the Tso Moriri
eclogites along the Indus Suture Zone are not erosionally driven (de Sigoyer et al. 2004; Leech
et al. 2005), a purely tectonic origin for the Greater
Himalaya is not currently favoured. Thermochronological transects across the Himalayan front
suggest that zones of heavier precipitation correlate
with areas of faster exhumation (Thiede et al. 2004;
Wobus et al. 2005), although some indicators have
been used to argue that rock uplift rather than
monsoon rains dominate as drivers of erosion
(Burbank et al. 2003). Furthermore, climaticallyfocused erosion appears to guide the location of
active faults along the Himalayan front (Wobus
et al. 2003). Our study reinforces the role of the
monsoon in controlling orogenic architecture in
the Himalaya. Without a strong summer monsoon
212
P. D. CLIFT ET AL.
Fig. 15. Diagram showing the variability in various sediment and environmental proxies since the Last Glacial Maximum. Sediments are from the Indus delta and the Indus
Canyon. (b) Nd data are from Clift et al. (2008). (c) Sr data are from Table 3. The Nd and Sr record are compared with (a) the GISP2 ice core climate record (Stuiver & Grootes 2000),
(d) the variations in organic carbon isotope composition and (e) the intensity of the SW monsoon traced by speleothem records from Qunf and Timta Caves (Fleitmann et al.
2003; Sinha et al. 2005) in Oman and by pollen (Herzschuh 2006) from across Asia (black line), and well as western Himalayan landslides (Bookhagen et al. 2005). Note rapid
change from C3 to C4 flora in early Holocene.
MONSOON CONTROL OVER EROSION
erosion is preferentially located in the Karakoram,
such as at the LGM. However, for the exhumation
of the Greater Himalaya to occur in the ways
recently proposed a summer monsoon is crucial
because the focused erosion required by such
models does not occur in its absence.
Our work also has implications for erosion/
tectonic coupling on a smaller scale. We show that
the Nanga Parbat metamorphic massif, located in
the western Himalayan syntaxis is a much less
impressive sediment producer than its eastern twin
at Namche Barwe, Tibet. France-Lanord et al.
(2006) and Stewart et al. (2008) used a combination
of thermochronological and U – Pb zircon data to
indicate that as much as 45% of the sediment in
the Brahmaputra is derived from erosion of the
Namche Barwe massif, representing only 2% of
the drainage system. In contrast, Nanga Parbat does
not seem to contribute more than c. 3% of the sediment reaching the Indus delta. Our data casts some
doubt over the idea that erosional unroofing by
the Indus is driving the exhumation of the deep
buried rocks (Zeitler et al. 2001) and that tectonic
exhumation processes might also be significant
(Hubbard et al. 1995). Why the two syntaxes
behave in such different ways is unclear, although
it is noteworthy that the Indus basin is much drier
and generally much less erosive than the eastern
Himalaya. Even within that region the effect of
monsoon rain strength is a primary control on
erosion rates (Galy & France-Lanord 2001).
Monsoon and the environment
The organic carbon data now for the first time allow
us to examine the changing environments in the
Indus drainage basin. Other climate indicators,
such as lake sediments (Enzel et al. 1999) from
the edge of the Thar Desert show that after the
Early Holocene maximum summer monsoon
strength declined towards the present day. The
d13C record from Keti Bandar shows significant correlation with the speleothem climate records
(Fig. 15). There is a minimum in d13C following
the Younger Dryas at c. 12 ka during the earliest
Holocene, and then a rapid rise in the Early Holocene. The low d13C values seen at 8.6 and 9.8 ka
are interpreted to indicate a dominant input from
rock-derived organic carbon, but even excluding
these points there is a rise d13C values during the
Early Holocene. We interpret the change in d13C
to reflect an increase in marine organic carbon flux
into the sediment at Keti Bandar, as result of the
marine transgression.
Interestingly, d13C stays high well after the speleothem records start to decline but then decreases
rapidly after c. 4 ka, when the sedimentation again
becomes fluvial. This indicates rapid reduction in
213
marine organic material after 4 ka. The carbon
isotope data suggest that the summer monsoons in
western India and Pakistan may not perfectly track
those affecting Arabia and recorded in the Oman
speleothem records (Fleitmann et al. 2003). The
change in carbon isotopes has occurred most dramatically in the last 4 ka, and does not decrease
gradually from 8 ka, as seen in the speleothems. A
more detailed study, especially one using biomarkers, would be required to determine in detail
when floral changes occurred, yet it is noteworthy
that lake records from the environs of the Thar
Desert show the most intense drying after 4.2 ka
and were preceded by a much wetter period prior
to that (Enzel et al. 1999).
Conclusions
In this study we employed a series of petrographic,
geochemical and isotopic methods to examine the
effect on climate change since 20 ka on the nature
of erosion and environmental conditions in
the Indus river basin. Although the mineralogy of
the sediments did not change much during this
time there are coherent changes towards more radiogenic Sr and unradiogenic Nd isotopes that reflect
increasing erosion of ancient crust between 12 and
8 ka. This represents the transition from Younger
Dryas to Early Holocene and is known as a period
when summer monsoon rains strengthened (Fleitmann et al. 2003). AFT data shows that since the
LGM the Indus preferentially eroded sources that
have younger ages compared to those at 20 ka
(more rapidly eroded sources). Ar–Ar mica dates
also show a shift to younger cooling ages at this
time and together with U –Pb zircon dating demonstrates that the greatest change has been a relative
decrease in erosion from north of the Indus Suture
(i.e. from the Karakoram and Transhimalaya) and
an increase in erosion from the Lesser Himalaya.
As these ranges now lie in the zone of heaviest
monsoon rains (Bookhagen & Burbank 2006) we
infer that the change in provenance deposited at
the delta is caused by erosion modulated by
monsoon intensity. We can rule out remobilization
of glacially eroded sediments. The close correlation
with the climate history also indicates that sediment
flux from source to delta was rapid and lower than
the uncertainties in the 14C dating. Carbon isotope
data also argue for a change in environmental conditions, with a sharp change to more positive
marine organic carbon values during the start of
the Holocene, as sea-level rose.
Minimum 1Nd values are followed by a moderate
increase after 9 ka, before a further decrease in the
past 250 years. We interpret this to reflect damming
of the main Indus at Tarbela blocking the flux of
214
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sediment from the suture zone. A drop in d13C
values starting around 4 ka indicates a shift
towards more terrestrial sources of organic carbon
in the Indus basin, as the coast prograded
southwards.
The sediment record in the delta shows that
erosion of the western Himalaya is strongly regulated by monsoon climate. Because current tectonic
models for the exhumation of high grade metamorphic rocks in the Greater Himalaya require
focused erosion our study suggests that formation
of that range is dependent not just on the presence
of tectonically thickened crust under southern
Tibet but also on the activity of a strong summer
monsoon. The pre-Holocene record shows that
without the summer rains erosion is focused
within and north of the Indus Suture and that consequently Himalayan exhumation cannot occur, at
least not in the ways presently favoured by structural
geologists.
We thank US National Science Foundation (Ocean
Sciences) for support of this project.
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