7dezileau Al Paleoc 2004
7dezileau Al Paleoc 2004
1029/2004PA001006, 2004
[1] Biogenic opal and organic carbon vertical rain rates in sediment cores reveal a strong cyclicity in the
productivity of the upwelling system off presently arid northern Chile during the last 100,000 years.
Changes in productivity are found to be in phase with the precessional cycle (20,000 years) and with
inputs of iron from the continent. During austral summer insolation maxima, increased precipitation and
river runoff in the region appear to have brought high inputs of iron, mainly from the Andes, to the coastal
ocean enhancing primary productivity there. We interpret our results as providing evidence for iron control
of past productivity in this upwelling system and for a tight link between productivity and orbital forcing at
midlatitudes. INDEX TERMS: 4267 Oceanography: General: Paleoceanography; 4825 Oceanography: Biological and Chemical:
Geochemistry; 4860 Oceanography: Biological and Chemical: Radioactivity and radioisotopes; KEYWORDS: paleoproductivity,
thorium-230, iron, coastal upwelling, biogenic opal, organic carbon
Citation: Dezileau, L., O. Ulloa, D. Hebbeln, F. Lamy, J.-L. Reyss, and M. Fontugne (2004), Iron control of past productivity in the
coastal upwelling system off the Atacama Desert, Chile, Paleoceanography, 19, PA3012, doi:10.1029/2004PA001006.
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Figure 1. Composite of annual average of phytoplankton pigment concentration (Chl) of the eastern
South Pacific and annual maximum normalized difference vegetation index (NDVI) of the central and
southern Andean region (both for year 2000). These data were derived from the SeaWiFS sensor
(SeaWiFS Project) Distributed Active Archive Center. Top left inset: map of the study area with location
of the two cores GeoB 3375-1 and GeoB 7101-1 (27280S, 71150W). Bottom left inset: chlorophyll and
nutrient profiles of the upper 100 m depth at station GeoB 3377-1 (27280S; 7131.50W). Right inset:
average of annual continental rainfall data in Chile (http://www.meteochile.cl). See color version of this
figure at back of this issue.
a relatively low primary production [Daneri et al., 2000], all sediments was measured by weighting a fixed sample
characteristics of iron limited HNLC systems [Hutchins and volume before and after freeze-drying (Table 1). Uranium
Bruland, 1998; Hutchins et al., 2002]. The modern climate and thorium concentrations were measured by a spectrom-
of the continental region adjacent to the sampling position etry following separation on anion exchange columns and
(the southern limit of the Atacama Desert) is hyperarid deposition onto aluminum foil. The analytical uncertainty of
(Figure 1). the 230Th concentration data from counting statistics was
[5] Core GeoB7101-1 was sampled at 10 cm intervals 5%. Samples were only occasionally run in duplicate and
using 10-ml syringes. Two samples series were taken. The uncertainties of the reproductibilities were less than or equal
first was designated for uranium, thorium (Table 1) and rare to those from counting statistics. The analytical uncertainty
Earth elements analyses and the second for carbonate of 238U concentration measurements from counting statis-
concentration measurements. The dry bulk density of the tics was 6%. The carbonate content (% CaCO3) has been
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Table 1. Results Obtained on Marine Sediment Samples for Cores GeoB 3375-1 and GeoB 7101-1a
GeoB 7101-1 Age, DBD, 238U, 232Th, 230Th, 230Thex, 230Thex, 238U auth, Geob 3375 Age, Org C, Opal, Detrital Material, Iron,
Depth, cm kyr g/cm3 dpm/g dpm/g dpm/g dpm/g dpm/g dpm/g Depth, cm kyr % % % ppm
3 9.7 0.87 1.51 ± 0.11 1.39 ± 0.11 3.94 ± 0.24 2.86 ± 0.25 3.13 ± 0.28 0.47 ± 0.13 3 9.7 0.43 ± 0.02 0.70 ± 0.14 81.94 26047
8 10.3 1.07 3.08 ± 0.18 1.41 ± 0.10 4.06 ± 0.24 2.82 ± 0.25 3.10 ± 0.28 2.02 ± 0.19 8 10.3 0.41 ± 0.02 0.60 ± 0.12 77.65 25997
18 12.2 1.05 5.03 ± 0.19 1.42 ± 0.10 4.08 ± 0.21 2.59 ± 0.22 2.90 ± 0.25 3.97 ± 0.20 18 12.2 0.52 ± 0.03 0.40 ± 0.08 74.07 24589
23 13.2 0.96 5.14 ± 0.22 1.47 ± 0.19 3.94 ± 0.37 2.38 ± 0.38 2.68 ± 0.43 4.04 ± 0.25 23 13.2 0.65 ± 0.03 0.30 ± 0.06 75.19 26123
33 15.2 1.00 3.88 ± 0.19 1.57 ± 0.10 4.02 ± 0.18 2.49 ± 0.19 2.86 ± 0.22 2.70 ± 0.20 33 15.2 0.53 ± 0.03 0.60 ± 0.12 80.90 27356
48 16.7 1.09 2.60 ± 0.55 1.95 ± 0.17 3.25 ± 0.25 1.62 ± 0.28 1.89 ± 0.33 1.13 ± 0.56 48 16.7 0.52 ± 0.03 0.75 ± 0.15 85.91 28353
63 18.1 1.18 2.15 ± 0.15 1.79 ± 0.15 2.90 ± 0.20 1.44 ± 0.22 1.70 ± 0.26 0.81 ± 0.17 63 18.1 0.48 ± 0.02 0.80 ± 0.16 87.73 28177
78 19.5 1.12 2.23 ± 0.12 2.03 ± 0.08 3.20 ± 0.12 1.56 ± 0.13 1.87 ± 0.15 0.71 ± 0.13 78 19.5 0.46 ± 0.02 0.75 ± 0.15 86.36 32282
93 21.1 1.14 2.14 ± 0.16 1.85 ± 0.13 2.67 ± 0.17 1.16 ± 0.19 1.40 ± 0.23 0.76 ± 0.18 93 21.1 0.48 ± 0.02 0.70 ± 0.14 87.64 34005
103 22.2 1.17 1.95 ± 0.08 1.72 ± 0.04 2.67 ± 0.06 1.26 ± 0.07 1.55 ± 0.09 0.66 ± 0.08 103 22.2 0.45 ± 0.02 0.80 ± 0.16 87.20 32400
128 25.2 1.11 2.69 ± 0.33 1.71 ± 0.12 3.01 ± 0.19 1.44 ± 0.22 1.81 ± 0.27 1.40 ± 0.34 128 25.2 0.75 ± 0.04 0.95 ± 0.19 85.00 32245
153 28.7 1.12 2.48 ± 0.11 1.57 ± 0.07 3.94 ± 0.15 2.46 ± 0.16 3.20 ± 0.20 1.30 ± 0.12 153 28.7 0.69 ± 0.03 1.10 ± 0.22 85.07 30279
163 30.0 1.16 2.93 ± 0.30 1.43 ± 0.05 3.58 ± 0.10 2.06 ± 0.12 2.71 ± 0.16 1.86 ± 0.30 163 30.0 0.80 ± 0.04 0.70 ± 0.14 81.09 25247
173 34.6 1.23 3.30 ± 0.07 1.57 ± 0.08 3.71 ± 0.15 1.95 ± 0.16 2.69 ± 0.22 2.13 ± 0.08 173 34.6 0.59 ± 0.03 0.60 ± 0.12 81.37 25740
178 36.9 1.23 3.65 ± 0.11 1.42 ± 0.06 3.63 ± 0.13 1.82 ± 0.14 2.56 ± 0.19 2.58 ± 0.11 178 36.9 0.41 ± 0.02 0.65 ± 0.13 79.41 24572
193 40.3 1.18 3.36 ± 0.10 1.36 ± 0.08 3.18 ± 0.14 1.43 ± 0.16 2.07 ± 0.22 2.35 ± 0.11 193 40.3 0.58 ± 0.03 0.60 ± 0.12 80.35 29429
208 42.7 1.17 2.32 ± 0.14 1.51 ± 0.09 2.81 ± 0.15 1.29 ± 0.17 1.91 ± 0.25 1.19 ± 0.15 208 42.7 0.58 ± 0.03 0.80 ± 0.16 81.47 28684
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223 47.2 1.18 2.73 ± 0.15 1.74 ± 0.14 2.85 ± 0.20 1.05 ± 0.22 1.62 ± 0.34 1.42 ± 0.17 223 47.2 0.69 ± 0.03 0.70 ± 0.14 83.40 31029
238 51.0 1.25 2.38 ± 0.09 1.94 ± 0.07 3.02 ± 0.10 1.21 ± 0.12 1.94 ± 0.19 0.93 ± 0.10 238 51.0 0.53 ± 0.03 0.80 ± 0.16 83.23 30481
253 54.8 1.18 2.63 ± 0.14 2.00 ± 0.13 3.69 ± 0.21 1.74 ± 0.23 2.88 ± 0.38 1.14 ± 0.16 253 54.8 0.65 ± 0.03 0.70 ± 0.14 79.53 26514
263 57.4 1.24 3.22 ± 0.16 1.62 ± 0.13 3.47 ± 0.23 1.43 ± 0.25 2.43 ± 0.43 2.00 ± 0.18 263 57.4 0.69 ± 0.03 0.50 ± 0.10 81.68 26040
273 59.9 1.29 2.38 ± 0.17 1.44 ± 0.09 3.37 ± 0.16 1.74 ± 0.19 3.02 ± 0.33 1.30 ± 0.18 273 59.9 0.60 ± 0.03 0.50 ± 0.10 83.15 26148
293 65.0 1.17 2.98 ± 0.07 1.39 ± 0.10 3.03 ± 0.17 1.11 ± 0.18 2.02 ± 0.33 1.94 ± 0.09 293 65.0 0.80 ± 0.04 0.70 ± 0.14 81.88 28981
313 69.8 1.24 2.88 ± 0.08 1.74 ± 0.06 3.03 ± 0.09 0.98 ± 0.10 1.87 ± 0.20 1.57 ± 0.09 313 70.5 0.58 ± 0.03 0.80 ± 0.16 83.86 32879
333 73.9 1.22 2.66 ± 0.20 1.88 ± 0.07 2.86 ± 0.10 0.83 ± 0.15 1.65 ± 0.30 1.24 ± 0.21 323 73.2 0.54 ± 0.03 0.70 ± 0.14 86.39 33223
343 75.9 1.24 2.38 ± 0.09 1.95 ± 0.07 2.97 ± 0.10 1.04 ± 0.12 2.10 ± 0.24 0.91 ± 0.10 333 75.9 0.63 ± 0.03 1.00 ± 0.20 87.84 33039
353 78.1 1.13 2.62 ± 0.12 1.76 ± 0.09 3.24 ± 0.14 1.26 ± 0.16 2.58 ± 0.33 1.31 ± 0.13 343 78.6 0.56 ± 0.03 1.40 ± 0.28 84.59 30914
DEZILEAU ET AL.: PAST PRODUCTIVITY OFF CHILE
363 80.3 1.19 2.95 ± 0.15 1.54 ± 0.06 3.17 ± 0.10 1.07 ± 0.13 2.25 ± 0.28 1.79 ± 0.15 353 81.4 0.67 ± 0.03 1.10 ± 0.22 80.10 28266
373 82.5 1.17 3.52 ± 0.13 1.33 ± 0.08 3.54 ± 0.17 1.20 ± 0.19 2.57 ± 0.40 2.53 ± 0.14 363 84.1 0.63 ± 0.03 1.00 ± 0.20 78.61 25225
383 89.5 1.11 3.85 ± 0.20 1.50 ± 0.10 3.57 ± 0.17 0.91 ± 0.22 2.08 ± 0.49 2.72 ± 0.20 383 89.5 0.50 ± 0.03 0.80 ± 0.16 78.03 28111
403 95.0 1.21 2.75 ± 0.13 1.77 ± 0.08 2.90 ± 0.11 0.74 ± 0.14 1.78 ± 0.34 1.42 ± 0.14 403 95.0 0.39 ± 0.02 1.00 ± 0.20 87.92 33803
409 96.4 1.25 2.45 ± 0.10 1.83 ± 0.11 2.89 ± 0.16 0.88 ± 0.18 2.13 ± 0.45 1.08 ± 0.12 408 96.4 0.50 ± 0.02 1.00 ± 0.20 87.21 31965
a
The dry bulk density (DBD) of the sediments was measured by weighting a fixed sample volume before and after freeze-drying. Uranium and thorium concentrations were measured by a spectrometry. 230Thex
refers to excess 230Th activity in sediments decay-corrected to the time of deposition. 238U auth refers to excess U above detrital background levels. The biogenic opal content was measured applying the method of
Müller and Schneider [1993]. Organic carbon analyses were conducted with an Hereaus CHN-O-rapid. The detrital fraction of the sediment was estimated from bulk sediment weight minus biogenic components.
The iron data have been previously published in the work of Lamy et al. [2000].
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PA3012 DEZILEAU ET AL.: PAST PRODUCTIVITY OFF CHILE PA3012
3. Chronology
[7] The age model for core GeoB 3375-1 is based on both
AMS 14C ages and @ 18O records of N. pachyderma (sin.)
[Lamy et al., 1998] resulting in an age of 117.000 cal
years BP at the base of the core (Figure 2). The chronology
for core GeoB 7101-1 has been obtained by correlating
graphically its carbonate content variations with those
of core GeoB 3375-1, using the Analyseries Software
[Paillard et al., 1996] (Figure 2). On this basis, core GeoB
7101-1 covers the last 100,000 cal years BP, with an
average sedimentation rate of 5 cm/1000 years. These twin
cores come from almost exactly the same location and have
the same age at each depth up to 300 cm. This suggests that
if these cores have been affected by sediment redistribu-
tions, these effects were of same intensities in the past.
Figure 2. Age model for sediment core GeoB 3375-1 and 4. Vertical Fluxes Calculations
GeoB 7101-1. (top) @ 18O(%) curve of the planktic [8] Although past changes in ocean productivity can be
foraminifera N. pachyderma (sin.) and age control points assessed, in principle, from the record of biogenic detritus
(indicated by triangle) include seven AMS 14C dates and buried in the seabed, their interpretation is often hampered
two graphical correlation points of the @ 18O records to a by sediment redistribution processes (focusing or winnow-
standard @ 18O curve. (bottom) Carbonate content for the ing) and variable dissolution. We have calculated preserved
cores GeoB 3375-1 and GeoB 7101-1. We obtained the vertical rain rates to the seafloor by normalizing biogenic
chronology for the core GeoB 7101-1 by graphically component fluxes to the corresponding excess 230Th activ-
correlating its carbonate content variations with those of ity in the sediments, a method that corrects for sediment
core GeoB 3375-1. The used standard methods for @ 18O focusing and winnowing [Bacon, 1984; Suman and Bacon,
analysis, AMS dating, and carbonate content determinations 1989; François et al., 1990, 2004].
are described elsewhere in detail [Lamy et al., 1998]. [9] Thorium-230 normalized flux calculations are based on
the assumption that the flux of 230Th to the seafloor is constant
and equal to the rate of production [Bacon, 1984; Suman and
determined with a calcimeter by the CO2 volumetric method.
Bacon, 1989; François et al., 1990, 2004]. Excess 230Th
The precision is estimated to be about 2%. Analyses of La
activity in settling particulates is then inversely related to total
and Yb were carried out by Epithermal Neutron Activation
mass flux, and excess 230Th activities (to see how is obtained
Analysis (ENAA) at the Pierre Sue Laboratory (Saclay,
the age-corrected excess 230Th activity see Appendix A) in
France). Two USGS standards, Mag 1 and A1, were used.
the sediment can be used as reference against which the flux
Sediment samples and standards were enclosed in plastic
of other sedimentary components can be estimated:
bags. After irradiation, sediment samples and standards
were measured with an HP Ge detector (FWMH 1.7 keV
b:Z:fi
at 1332 keV; relative efficiency: 20%) at the Laboratoire des Fi ¼ 230 ; ð1Þ
Sciences du Climat et de l’Environnement. The precision is Thex
estimated to be about 5%.
[6] The biogenic opal content was measured on core where Fi is the normalized rain rate of the sedimentary
GeoB 3375-1 (D. Hebbeln, unpublished results, 2001) component i; b is the constant production rate of 230Th in
applying the method of Müller and Schneider [1993] and the water column (2.63 105 dpm cm3 kyr1); Z is the
the values obtained were between 0.3 and 1.4%. For water depth (cm); fi is the percentage of the sedimentary
samples with low opal contents (<1 wt %) the uncertainty component i; and 230Thex is the activity of decay- and
of the method used is of 20% and for samples with very low ingrowth-corrected excess 230Th in sediment.
opal contents (<0.5 wt %) the uncertainty is about 60% [10] Arguments for the validity of this approach have
(Table 1). Organic carbon analyses of core GeoB 3375-1 been examined elsewhere [Henderson et al., 1999; Yu et al.,
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Table 2. Vertical Flux Refers to 230Th Normalized Total Mass Accumulation Rate, Organic Carbon (Opal and Iron) Vertical Flux Refers
to 230Th Normalized Organic Carbon (Opal and Iron) Accumulation Ratea
Org C Opal Iron
Vertical Flux Vertical Flux Vertical Flux Vertical Flux Authigenic Uranium
Age, 230Thex, (230Th Method), (230Th Method), (230Th Method), (230Th Method), Accumulation Rate,
Kyr dpm/g g/cm2/kyr mg/cm2/kyr mg/cm2/kyr mg/cm2/kyr Opal/CaCO3 dpm/cm2/kyr
9.7 3.13 ± 0.28 1.64 ± 0.14 7.09 ± 0.62 11.51 ± 1.01 42.82 ± 3.77 0.044 ± 0.009 3.48
10.3 3.10 ± 0.28 1.66 ± 0.15 6.75 ± 0.60 9.97 ± 0.89 43.20 ± 3.85 0.029 ± 0.006 10.96
12.2 2.90 ± 0.25 1.77 ± 0.15 9.13 ± 0.78 7.09 ± 0.61 43.58 ± 3.74 0.017 ± 0.003 21.14
13.2 2.68 ± 0.43 1.92 ± 0.31 12.42 ± 2.01 5.75 ± 0.93 50.07 ± 8.09 0.013 ± 0.003 19.65
15.2 2.86 ± 0.22 1.80 ± 0.14 9.46 ± 0.73 10.79 ± 0.84 49.20 ± 3.82 0.035 ± 0.007 28.01
16.7 1.89 ± 0.33 2.72 ± 0.47 14.02 ± 2.42 20.41 ± 3.52 77.17 ± 13.31 0.064 ± 0.013 12.83
18.1 1.70 ± 0.26 3.02 ± 0.46 14.54 ± 2.21 24.19 ± 3.67 85.20 ± 12.94 0.080 ± 0.016 9.91
19.5 1.87 ± 0.15 2.76 ± 0.23 12.69 ± 1.04 20.69 ± 1.69 89.04 ± 7.26 0.065 ± 0.013 7.64
21.1 1.40 ± 0.23 3.66 ± 0.60 17.72 ± 2.90 25.63 ± 4.19 124.53 ± 20.36 0.069 ± 0.014 8.26
22.2 1.55 ± 0.09 3.33 ± 0.19 14.94 ± 0.84 26.63 ± 1.49 107.84 ± 6.04 0.075 ± 0.015 6.39
25.2 1.81 ± 0.27 2.84 ± 0.43 21.31 ± 3.21 26.99 ± 4.07 91.60 ± 13.81 0.081 ± 0.016 11.15
28.7 3.20 ± 0.20 1.61 ± 0.10 11.11 ± 0.71 17.69 ± 1.13 48.70 ± 3.10 0.094 ± 0.019 10.53
30.0 2.71 ± 0.16 1.90 ± 0.11 15.11 ± 0.91 13.28 ± 0.80 47.91 ± 2.89 0.044 ± 0.009 4.74
34.6 2.69 ± 0.22 1.92 ± 0.15 11.23 ± 0.91 11.50 ± 0.93 49.31 ± 3.98 0.037 ± 0.007 5.74
36.9 2.56 ± 0.19 2.01 ± 0.15 8.23 ± 0.62 13.08 ± 0.98 49.44 ± 3.70 0.040 ± 0.008 13.98
40.3 2.07 ± 0.22 2.48 ± 0.27 14.33 ± 1.55 14.88 ± 1.61 72.96 ± 7.91 0.035 ± 0.007 17.02
42.7 1.91 ± 0.25 2.69 ± 0.35 15.62 ± 2.01 21.50 ± 2.77 77.10 ± 9.93 0.050 ± 0.010 4.68
47.2 1.62 ± 0.34 3.18 ± 0.67 22.10 ± 4.64 22.29 ± 4.68 98.80 ± 20.73 0.051 ± 0.010 6.58
51.0 1.94 ± 0.19 2.65 ± 0.25 14.07 ± 1.34 21.20 ± 2.02 80.79 ± 7.70 0.056 ± 0.011 4.55
54.8 2.88 ± 0.38 1.79 ± 0.24 11.61 ± 1.54 12.50 ± 1.66 47.37 ± 6.30 0.039 ± 0.008 5.27
57.4 2.43 ± 0.43 2.12 ± 0.37 14.67 ± 2.59 10.58 ± 1.87 55.11 ± 9.72 0.032 ± 0.006 9.76
59.9 3.02 ± 0.33 1.70 ± 0.18 10.28 ± 1.11 8.51 ± 0.92 44.50 ± 4.80 0.034 ± 0.007 6.59
65.0 2.02 ± 0.33 2.55 ± 0.41 20.36 ± 3.30 17.84 ± 2.89 73.85 ± 11.98 0.047 ± 0.009 9.50
69.8 1.87 ± 0.20 2.75 ± 0.29 15.89 ± 1.66 21.99 ± 2.30 90.37 ± 9.45 0.059 ± 0.012 9.55
73.9 1.65 ± 0.30 3.12 ± 0.56 16.78 ± 3.03 21.84 ± 3.94 103.64 ± 18.72 0.062 ± 0.012 7.42
75.9 2.10 ± 0.24 2.45 ± 0.28 15.53 ± 1.80 24.50 ± 2.84 80.94 ± 9.39 0.108 ± 0.022 5.18
78.1 2.58 ± 0.33 1.99 ± 0.25 11.09 ± 1.40 27.93 ± 3.53 61.66 ± 7.79 0.113 ± 0.023 6.76
80.3 2.25 ± 0.28 2.28 ± 0.29 15.31 ± 1.92 25.13 ± 3.15 64.57 ± 8.10 0.066 ± 0.013 9.78
82.5 2.57 ± 0.40 2.00 ± 0.32 12.63 ± 1.99 20.04 ± 3.15 50.56 ± 7.95 0.054 ± 0.011 4.17
89.5 2.08 ± 0.49 2.47 ± 0.58 12.44 ± 2.93 19.74 ± 4.65 69.37 ± 16.34 0.041 ± 0.008 11.08
95.0 1.78 ± 0.34 2.90 ± 0.56 11.18 ± 2.17 28.97 ± 5.61 97.93 ± 18.98 0.101 ± 0.020 7.37
96.4 2.13 ± 0.45 2.41 ± 0.51 11.97 ± 2.52 24.13 ± 5.08 77.13 ± 16.24 0.097 ± 0.019 5.74
a
The authigenic uranium accumulation rate is estimated by multiplying the total mass accumulation rate (g cm2 kyr1) with the authigenic uranium
concentration (dpm g1).
evidence that the signal we observe is due to changes in 3375-1 in order to know if variable dissolution of CaCO3
preservation. occurred (X. Mohtadi et al., manuscript in preparation,
5.3.3. Opal//CaCO3 Ratio 2004). Mohtadi finds that the preservation of the plank-
[17] We have used the opal/CaCO3 ratio as another tonic forams is generally good to very good.
index of productivity (Figure 5c). This ratio gives an idea [18] To sum up, we do not want to argue that preservation
about the siliceous/carbonate productivity, taking into has had no effect on our data, but the similar pattern for all the
account that when the productivity increases in a region paleoproductivity indicators we studied, brings us to the
this ratio generally increases. However, there are some conclusion that we really see a paleoproductivity signal in
uncertainties, which can induce false conclusions when the data.
evaluating paleoproductivity from the opal/CaCO3 ratio.
Both opal and carbonate may be variably dissolved and 5.4. Authigenic Uranium: Proxy for Export
the opal/CaCO3 ratio can be controlled by dissolution. Productivity?
Opal and carbonate respond differently to dissolution, as [19] In oxic pore water, U is present as a soluble carbon-
carbonate is dissolved under more acidic conditions, ate complex. When conditions become sufficiently reducing
while opal gets dissolved under basic conditions. Thus to initiate sulphate reduction, U is reduced to an insoluble
dissolution problems can be considered negligible only if form and precipitates. The U added to the sediment by this
the Opal/CaCO3 record closely parallels the other paleo- process (referred to as authigenic U) accumulates at a rate
productivity proxies. Here, there is a good correlation that depends on the level of oxygen in bottom water and on
between the Opal/CaCO3 record and the organic carbon the flux of organic carbon. Kumar et al. [1995] showed a
and opal vertical flux. Therefore we do not have any positive relationship between organic carbon flux (export
evidence that the opal/CaCO3 ratio in our core has been productivity) and the accumulation rate of authigenic ura-
controlled by dissolution. Moreover, M. Mohtadi (Uni- nium and, assuming that a similar relationship existed in the
versity of Bremen, Germany) has counted and analyzed past, proposed that down-core records of authigenic U flux
planktonic foraminifera assemblages in the core GeoB could be used to constrain past changes in the flux of carbon
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Figure 5. Comparison of geochemical data for the last 100,000 years derived from deep-sea sediment
cores GeoB 3375-1 and GeoB 7101-1. (a) Organic carbon and (b) biogenic opal vertical rain rates based
on point-by-point normalization to 230Thex . (c) Biogenic opal/carbonate ratio is also a proxy for
productivity. (d) Iron content (dotted line) and iron vertical rain rates (line) based on point-by-point
normalization to 230Thex . Terrigenous particle origin can be determined by using the Fe/Al ratio. The
Fe/Al (line) (and La/Yb square) ratio of basaltic-andesitic rocks as found in the Andes is characterized by
a value above 0.45 (9.5) and the Fe/Al (La/Yb) ratio of acidic-plutonic rocks, as found in the coastal
range is characterized by a ratio under 0.45 (9.5). Measured Fe/Al ratios clearly show a higher
contribution of terrigenous particles from the Andes during (e) precessional (summer insolation) maxima.
to the deep sea. Thus we have decided to estimate authi- Holocene/MIS 2 periods, the authigenic U fluxes are high
genic U flux in the core GeoB 7101-1 in order to see more (6 – 27 dpm cm2 kyr1) (Figure 6). Unlike opal and
productivity proxies. organic carbon rain rates, the authigenic U flux do not
[20] During the MIS 4 – 5, accumulation rates of authi- reveal a cyclicity. Variations of authigenic U fluxes are
genic uranium are low (7 dpm cm2 kyr1) and during the erratic and do not show any climatic signals. How can we
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Figure 6. Comparison between authigenic uranium fluxes (dpm cm2 kyr1) and total and vertical
organic carbon fluxes (mg cm2 kyr1) for the last 100,000 years derived from deep-sea sediment core
GeoB 7101-1.
reconcile authigenic U flux with opal and organic carbon? authigenic U. Thus variation in authigenic U in our cores
The recent discovery that authigenic U fluxes may also be may also be explained by a change in the contribution of
influenced by lateral transport of organic carbon, or a PNU due to a change in the water column oxygen concen-
change of oxygen concentration in water column [François tration. In conclusion, we suggest that the authigenic U flux
et al., 1997; Anderson et al., 1998; Frank et al., 2000; cannot be used as a direct proxy of palaeoproductivity in the
Dezileau et al., 2002], helps reconcile the authigenic U flux eastern South Pacific.
record with those of the other proxies.
[21] The flux of organic carbon to the seabed may be
influenced by sediment focusing. That is, focused depo- 6. Discussion
sition of sinking particles by deep-sea currents may 6.1. Regional Paleoceanographic and Paleoclimatic
enhance significantly the local flux of organic matter to Implications
the seabed relative to the regional average flux of organic [23] Biogenic opal and organic carbon vertical rain rates
matter exported from surface waters [Anderson et al., and the opal/carbonate ratio (Figures 5a – 5c) reveal a
1998; François et al., 1993]. Accumulation of sediments strong cyclicity, which is dominated by precession (a
in the continental slope off northern Chile is strongly cycle of 20,000 years). High and low values are in
enhanced by sediment focusing. Lateral transport estima- phase with summertime (January) insolation maxima and
tions for the last 100 kyr suggest that sediment redistri- minima, calculated for 25S latitude from the Earth’s
bution is higher during the LGM and Holocene periods. known orbital variations [Berger and Loutre, 1991]. These
In that case, we suggest that a significant part of the variations were in phase during the last 100,000 years.
authigenic U was attributed to intense sediment focusing Iron vertical rain rates also show a strong precessional
during these periods (Figure 6). cyclicity. The patterns of iron vertical rain rate and of
[22] In the water column, particulate nonlithogenic U iron content itself (Figure 5d) are remarkably similar to
(PNU: excess U above detrital background levels) is found the down-core records of the proxies for biogenic pro-
in marine particulate matter [Anderson, 1982]. Zheng et al. ductivity (Figures 5a – 5c), suggesting iron availability to
[2002] have recently shown that PNU formed in surface be a factor responsible for past changes in productivity.
waters may, under certain circumstances (i.e., low concen- Although Fe/Al ratios could be affected by the presence
tration of oxygen in the water column), contribute signifi- of authigenic iron, particularly in low oxygen environ-
cantly to the total burial of authigenic U (between 20% and ments, variations in the La/Yb ratios (Figure 5c), which
80% below the oxygen minimum zone (OMZ) off Califor- are not altered by changes in the redox conditions, show
nia). Our two gravity cores were raised below the OMZ, the same pattern (see section 5.2). Thus our results
thus, the PNU must certainly contribute significantly to the indicate that the supply of iron and consequently biolog-
total burial of authigenic U in this area. Moreover, Zheng et ical productivity has varied in response to past changes in
al. [2002] showed that the preservation of PNU as particles orbital forcing.
sink through the water column varies with the water column [24] The potential for fertilization of iron-limited waters
oxygen content. Evidence for past changes in oxygen depends on the source of the iron. Iron supplied in the
concentration in the water column off Peru have been form of riverine or atmospheric dust is more likely
shown by Ganeshram et al. [2000]. This means that the biologically available at the surface than iron from other
oxygen content of the water column off northern Chile have sources (e.g., lithogenic material transported by deep-
also probably changed between glacial/interglacial periods ocean currents, for example). Recent studies [Lamy et
affecting the contribution of PNU to the total burial of al., 1998, 2000] on core GeoB 3375-1 have clearly
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corresponding high rates of export of carbon to the depth, ciently available in the ocean surface waters, limiting
upwelling promotes also a strong outgassing of CO2 to primary productivity in the region.
the atmosphere. Hence increased upwelling and primary
production do not necessarily mean a significant net
increase in uptake of atmospheric CO2. We have shown Appendix A: Calculating Age-Corrected Excess
here that past changes in productivity in the upwelling 230Th Activity at the Time of Deposition
system of the eastern South Pacific may have been
controlled mainly by the availability of Andean iron, [37] There are two prerequisites for utilization of 230Th
through changes in the hydrological conditions, and that data to determine vertical rain rates. First, the measured
this availability has been tightly linked to orbital forcing concentrations of 230Th have to be corrected both for
during the last 100,000 years. Therefore variations in detrital and authigenic contributions produced from decay
paleoproductivity in major coastal upwelling systems of 234U in the sediment in order to calculate the amount of
230
due to iron fertilization may have had a significant Th originating from scavenging in the oceanic water
influence on past variations in atmospheric pCO2. How- column (excess concentrations). Second, an independent
ever, we also show that the Chilean upwelling region timescale for the core is necessary to calculate the
never really has been highly productive in comparison corresponding value at the time of deposition, (230Thex),
with other upwelling regions or the Southern Ocean in for each measured 230Thex content.
view of the very low biogenic opal deposition and low [38] The total 238U measured in the samples consists of
Corg contents. Thus the potential importance of this two components: uranium present in detrital minerals
region as an area of glacial CO2 drawdown has most (238Ud) and authigenic uranium (238U auth) derived from
likely been negligible. This is, however, an important seawater.
result because it has been argued that the middle and low [39] Detrital uranium (238Ud) is estimated as:
latitude HNLC areas of the oceans such as the coastal
upwelling regions may have been an important sink for
glacial atmospheric CO2. 238
Ud ¼ 238
U=232 Th 232
Th; ðA1Þ
d
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Figure 1. Composite of annual average of phytoplankton pigment concentration (Chl) of the eastern
South Pacific and annual maximum normalized difference vegetation index (NDVI) of the central and
southern Andean region (both for year 2000). These data were derived from the SeaWiFS sensor
(SeaWiFS Project) Distributed Active Archive Center. Top left inset: map of the study area with location
of the two cores GeoB 3375-1 and GeoB 7101-1 (27280S, 71150W). Bottom left inset: chlorophyll and
nutrient profiles of the upper 100 m depth at station GeoB 3377-1 (27280S; 7131.50W). Right inset:
average of annual continental rainfall data in Chile (http://www.meteochile.cl).
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