Evidence of Poor Bottom Water Ventilation during LGM in the Equatorial Indian Ocean

Introduction

The depositional conditions in the marine environment can be oxic, suboxic and anoxic based on the presence or absence of oxygen at the sediment-water interface. Redox sensitive elements have demonstrated their potential in deciphering the past bottom water anoxic condition in the oceanic basin. The elemental concentrations in marine sediments are mainly controlled by various processes such as terrestrial influx, biological processes, in-situ precipitation, and/or by hydrothermal activity (Pattan and Pearce, 2009). The oxygen concentration in bottom water plays an important role in altering oxygen gradients in the sedimentary column and this in turn depends upon change in deep water circulation during the past glacial-interglacial period (Bareille et al., 1998; Ahmad et al., 2008; Pattan and Pearce, 2009).

Based on the dissolved oxygen (O₂) and/or hydrogen sulfide (H₂S) concentrations, the sedimentary environment has been categorized as oxic (>2.0 ml O₂ l⁻¹), suboxic/dysoxic (2.0–0.2 ml O₂ l⁻¹), and anoxic/euxinic (0.2–0 ml O₂ l⁻¹) (Tyson and Pearson, 1991). In addition to oxygen concentration, the labile organic matter (OM) also controls the redox element cycling in the bottom water. Under oxic conditions, aerobic bacteria utilizes dissolved oxygen for OM degradation, while with decrease in dissolved O₂, the degradation continues using secondary oxidant sources leading to oxygen deficient conditions in the water column. Redox sensitive elements are often portrayed as classic tool to reconstruct the past depositional conditions in the bottom water (Brumsack, 1980, 2006; Calvert and Pedersen, 1993; Dean et al., 1999; Algeo and Tribovillard, 2009). The redox elements such as Mo, V, Cr, Mn have different solubilities in marine water depending on the redox conditions and has been commonly used to trace anoxic conditions near the sediment-water interface (Agnihotri et al., 2003; Rimmer, 2004; Algeo and Lyons, 2006; Tribovillard et al., 2006; Banerji et al., 2016). In oxic waters, Mn gets precipitated as Mn-oxides into the sediments, while V as vanadate oxyanions (${\text{HVO}}_4^{2-}$ and H₂VO⁴⁻), Mo as molybdate (${\text{MoO}}_4^{2-}$) Cr as chromate anions (${\text{CrO}}_4^{2-}$) are present in dissolved form. Unlike Mn, all other redox sensitive elements are conservative in oxygenated waters with a constant concentration, but under anoxic conditions they are highly enriched in sediments especially where bottom water oxygen is zero (Calvert and Pedersen, 1993, 1996; Algeo and Lyons, 2006; Tribovillard et al., 2006; Pattan and Pearce, 2009).

The Indian Ocean being situated in mid-way of global conveyor belt, between the Atlantic deep water formation and return of surface water from the Pacific, deep waters in the Indian Ocean are ventilated only from south (Piotrowski et al., 2009). Presently, in the Northern Indian Ocean (NIO), intermediate depths comprises high salinity water masses such as Red Sea, Persian Gulf Waters and contribution from Pacific Ocean through Indonesian Archipelago at depths of 500 to 1,500 m (Kallel et al., 1988). The Indian Ocean deep water is mainly North Atlantic Deep Water (NADW) between ~2,000–4,000 m relatively rich in dissolved oxygen compared to Antarctic Bottom Water (AABW) found below ~4,000 m (Sarkar et al., 1993). Various studies have shown that during last glacial period, the formation rate of the NADW was reduced, while the AABW remained unchanged or probably enhanced (Duplessy et al., 1988; Ahmad et al., 2008).

High resolution paleoclimatic records from late-Quaternary sediments has become increasingly useful tool for deciphering variability in sedimentary paleoproductivity and paleoredox conditions (Ivanochko and Pedersen, 2004; Hendy and Pedersen, 2005; Dean et al., 2006; Cartapanis et al., 2011). A study based on organic carbon (OC) and Mn concentrations from the Arabian Sea, suggested deposition of sediments under oxic conditions during deglacial period as a result of lower productivity and high Mn concentration (Shetye et al., 2014). The prevalence of near anoxic bottom water conditions during glacial cycle has been demonstrated based on U and OC content in marine sediment from the SE Arabian Sea (Sarkar et al., 1993). Study based on Mo and V concentrations near the SE Arabian Sea suggested prevalence of suboxic conditions during LGM (Pattan and Pearce, 2009). During LGM, reduced proportion of NADW and increased proportion of AABW near the equatorial Indian Ocean has been inferred on the basis of Nd-isotopic composition of ferromagnese oxides and δ¹³C of foraminifera implying a major trigger in the development of oxygen deficient bottom conditions (Piotrowski et al., 2009). There have been substantial studies indicating the development and persistence of oxygen deficient conditions in the Northern Indian Ocean that are related to either productivity or change in bottom water conditions (Naqvi, 1987; Pailler et al., 2002; Rao et al., 2010). However, there remains unaddressed issues on the simultaneous signatures of productivity and bottom water anoxia on redox sensitive elements. Thus, to address the role of productivity and thermohaline ventilation during glacial-interglacial periods, a sediment core (SK-304A/05) from the intermixing zone of two distinct basins of NIO near the equatorial region was geochemically investigated. This study attempts to substantiate the influence of both productivity and the bottom water ventilation during glacial-interglacial period near the equatorial region of NIO. The objectives of the present study is (i) to reconstruct the redox conditions during glacial-interglacial periods and (ii) to identify the variations in the bottom water oxygen conditions with its causative mechanism during the last 25 ka years BP.

Present Day Oceanographic Setting

The Northern Indian Ocean is unique compared to the other oceans due to its topographical setting as it comprises two basins i.e., the Arabian Sea and the Bay of Bengal being separated by Indian subcontinent. The land-ocean thermal contrast leads to seasonal reversal of winds. During summer (June-September) the monsoonal winds are south-westerly (SW) and during winter (November-February) the monsoonal winds are north-easterly (NE) (Tomczak and Godfrey, 2003). In response to wind, surface currents also reverses its direction in the equatorial Indian Ocean. During summer monsoon, a branch of Somali current (SC) at 4° turns offshore and supplies the summer monsoon current (SMC) flowing eastward. In addition to SC, the SMC also receives water from southward flowing West Indian Coastal Current (WICC) (Tiwari et al., 2006). As SMC reaches Sri Lanka, it turns northward to Bay of Bengal by flowing around the cyclonic Sri Lanka Dome (SD) and feeding the northeastward flowing East Indian Coast Current (EICC) (Tiwari et al., 2006). Thus, the SMC along with the WICC flows from west to east transporting highly saline water from the Arabian Sea to the Bay of Bengal. During winter monsoon, EICC reverses its direction and flows in southwest direction feeding low salinity water to the west flowing northeast monsoon current (NMC), which in turn contributes to northward flowing WICC (Schott and McCreary, 2001). Thus, these currents play a crucial role in nutrient distribution and chlorophyll concentrations in the equatorial regions (Vidya et al., 2013).

Geochemical investigations have shown that the equatorial Indian Ocean, off Sri Lanka is largely composed of calcareous and smectite clays (Nath, 2001). The sediment trap study carried out for the measurement of biogenic fluxes in the Northern Indian Ocean found predominance of opal fluxes at western Arabian Sea and the Bay of Bengal. But the eastern Arabian Sea, the southern Bay of Bengal (SBBT), and the equatorial Indian Ocean (EIOT) traps are dominated by carbonate fluxes (Ramaswamy and Gaye, 2006). Strong seasonality in the biogenic flux has been observed at SBBT while EIOT remained deprived of such seasonal variations (Vidya et al., 2013).

Methodology

A ~410 cm gravity core (SK-304A/05; water depth—3,408 m) was raised off Srilanka (05°45.622′ N; 79°24.763′ E) in the equatorial Indian Ocean during the ORV Sagar Kanya cruise SK-304 in March 2013 (Figure 1). The core was sub-sampled at 1 cm interval with non-metallic knife to avoid metallic contamination and kept in a clean ziplock bags till further analysis. Subsamples were oven dried at 80°C and finely powdered with the help of agate mortar and pestle for its biogenic, geochemical and isotopic analysis.

FIGURE 1

Figure 1. Bathymetry map of Northern Indian Ocean with SK-304A/05 sediment core location retrieved during onboard ORV Sagarkanya. The sediment core lies at the mixing zone of the Arabian Sea and the Bay of Bengal near equatorial region.

The chronology for the upper 200 cm of the core was established based on nine AMS radiocarbon dates (¹⁴C) analyzed at NSF-AMS facility of Arizona University, USA on handpicked mixed planktonic foraminifera from different depths. The ¹⁴C dates were calibrated by Calib 7.0.2 using Marine13 calibration curve (Stuiver et al., 1998; Reimer et al., 2009, 2013) and were corrected with a reservoir age correction of ΔR 60 ± 52 years (Dutta et al., 2001; Southon et al., 2002).

In order to measure the trace elemental concentrations, ~300 mg of the dried and crushed samples was subjected to closed digestion by treating it with acid mixture (HNO₃, HCl, and HF) in microwave digestion system (Milestone, Start D). Trace elemental (Ti, Mo, V, Cr, Co, Mn) concentrations were measured by aspirating the digested solution in ICP-MS (Thermo-X series2). The accuracy and precision for the analysis were monitored by repeat measurements of reference sediment standards (marine sediment standards MAG-1 and NOVA) and was found to be better than ±6 and ±4% respectively. Calcium carbonate (CaCO₃) was analyzed on Coulometer (UIC Coulometer, Model 5012) with a precision of ~2%. Total organic carbon (OC) and total nitrogen (TN) was measured using NC Elemental Analyzer (Flash 2000) with a precision better than 0.2 and 2% respectively (Bhushan et al., 2001).

Results

Chronology

Table 1 summarizes detailed AMS ¹⁴C chronology results of the studied sediment core SK-304A/05 retrieved from the equatorial Indian Ocean. The reconstructed age-depth model for the sediment core based on the calibrated radiocarbon dates of foraminifers at various depths (upper 200 cm section) provides paleoclimatic records for the last 25 ka years BP (Figure 2). The sediment deposition rate at the core varies from ~5.0 to 13.8 cm.ka⁻¹. The highest and the lowest sedimentation rates were observed between ~8 to 11 ka years BP and ~13.5 to 19.5 ka years BP respectively. An average sedimentation rate of ~8 cm.ka⁻¹ was observed for the studied sediment core (Figure 2). The late-Quaternary period has been broadly divided into Last Glacial Maxima (LGM: 22.5–17.5 ka years BP), Deglacial Period (DP: 17.5–11 ka years BP), and Holocene Period (HP: 11-Present) (Rao et al., 2010).

TABLE 1

Table 1. Calibrated radiocarbon ages for the sediment core SK-304A/05.

FIGURE 2

Figure 2. Age-depth model of AMS dates of foraminifers at selected depth of the sediment core SK-304A/05. Linear interpolation of sedimentation rates is assumed based on the AMS dates.

Geochemical Proxies

The downcore geochemical signatures were studied to reconstruct the paleoproductivity and paleoredox conditions prevailed during the last 25 ka years BP. Generally, Al and Ti are considered as extremely resistant to weathering and conservative elements as they remain unaffected due to changes in redox conditions (Nesbitt and Markovics, 1997; Wei et al., 2003) and has been extensively used to estimate the terrigenous material in the sedimentary environment (Murray and Leinen, 1993, 1996; Schroeder et al., 1997; Klump et al., 2000). Under certain circumstances, Al can form as a result of authigenic clay mineral formation (Timothy and Calvert, 1998) or it may get scavenged as hydroxides coating over biogenic particles (Murray and Leinen, 1996). Similar to Al, Si is also associated with biogenic opal and this limits its use as terrestrial tag. Thus, in the present study, the elements have been normalized by Ti instead of Al and Si. The Ti concentration in the studied sediment core varies between 1,923–3,585 ppm (Figure 3). Sedimentary OC and CaCO₃ are important constituents of the biogenic fraction of the marine sediments, and thus can be used as a proxy for paleoproductivity. However, OC and CaCO₃ constitute only a fraction of total biological productivity in the surface oceanic water due to its biological degradation during its passage through the water column (Tribovillard et al., 2006). The OC and CaCO₃ concentration ranges from 1.28–5.14 to 25.30–48.92 wt% respectively (Figures 4, 5). High OC concentration results in enhanced bacterial degradation causing oxygen deficient conditions (suboxic, anoxic, and euxinic) in the water column and at sediment-water interface. Under such oxygen deficient conditions at the sediment-water interface, the behavioral pattern of redox sensitive elements is generally used to comprehend the paleoredox conditions persisted at the time of sediment deposition. The elemental concentration of V, Mn, Cr, Mo, Ni, Co that has been used to access the paleoredox conditions ranges from 45–110, 204–380, 45–91, 0.6–2.8, 35–90, and 7–15 ppm respectively (Figures 3, 4).

FIGURE 3

Figure 3. Downcore variation of elemental concentration in the sediment core SK-304A/05 indicates low terrestrial flux during LGM with gradual increasing values during Deglacial and Holocene period. The dotted line in each plot indicates average crustal values for the respective elements.

FIGURE 4

Figure 4. Downcore variation of Mn, CaCO₃, and Mn/Ti indicates that Mn forms authegenic carbonate in presence of CaCO_3.

FIGURE 5

Figure 5. Downcore variation of Ti normalized redox sensitive elements (Co, Ni, V, Mo), OC and OC flux. High values of OC and redox sensitive elements observed during LGM.

Discussion

The organic matter (Shetye et al., 2014) and Fe- and Mn- oxyhydroxides (Tribovillard et al., 2006) are the major sources for the transportation of the trace elements from water column to the sediments. In oxic and anoxic environments, the trace elements behave differently based on their oxidation states which is influenced by the redox conditions (Shetye et al., 2014).

Biogenic Productivity during Glacial Interglacial Periods

Consistently high values for the CaCO₃ (Figure 4) were observed during LGM with gradually declining trend during the early Holocene and subsequently marginal increase during the late Holocene. Such consistently high values suggest high calcareous productivity during LGM. Two conspicuous peaks of OC (Figure 5) during ~21 ka years BP and at early Holocene (11–8 ka years BP) has been observed. The early Holocene OC peak corroborates well with the abrupt increase in the sedimentation rate ~13.5 cm.ka⁻¹ primarily suggesting preservation of OC with efficient burial and not due to abrupt high overhead productivity. The OC peak at ~21 ka years BP corresponding to LGM period, however, resulted due to high productivity and better OC preservation. High OC and CaCO₃ observed during LGM can be due to high productivity because of strong NE monsoonal winds that enhanced nutrient levels in the photic zone (Rostek et al., 1997; Punyu et al., 2014). With the commencement of deglacial period, weakening of NE monsoonal winds led to decrease in productivity during the Holocene period. Thus, high productivity could be one of the factors responsible for triggering reducing conditions at the sediment-water interface (Tribovillard et al., 2006).

Redox Proxy with Detrital Affect

Generally, Cr is present in the form of Cr (VI) as mobile chromate anion in oxygenated waters, while under anoxic conditions it gets reduced to Cr (III), which is very unstable and forms complex cations with humic and fulvic acids. It also gets adsorbed with Fe-Mn oxyhydroxides and transported to the sediments (Calvert and Pedersen, 1993; Tribovillard et al., 2006). Cr also gets transported to the sediments along with the detrital fraction due to its presence in chromite and ferromanganese minerals (Dill et al., 1988; Francois, 1988; Hild and Brumsack, 1998). The average Cr concentration in the studied sediment core is ~69 ppm, much higher than the average crustal value of 35 ppm (Taylor and McLennan, 1995). Synchronous variation in vertical profiles of detrital proxies Ti and C/N along with Cr has been observed in this study (Figure 3). Consistent low values of Ti and Cr till 18 ka years BP with C/N <12 suggests reduced terrestrial contribution at the core location due to weakening of summer monsoon (Naidu and Malmgren, 1996; Rashid et al., 2007; Anand et al., 2008). Gradual increase in Ti and Cr after 18 ka years BP till 8 ka years BP with C/N ≥12 indicates enhanced land-driven clastic fraction to the region instigated by the summer monsoon intensification (Govil and Naidu, 2011). The Cr concentrations in the studied sediment core is thus a function of changing detrital influx to the region rather than changing redox conditions in the water column and limits its application as redox proxy, but can be a potential proxy to decipher terrestrial influence.

Co has been used as potential tool to decipher paleoredox conditions at the sediment-water interface due to its complex formation with fluvic or humic acid under oxic seawaters (Achterberg et al., 2003). In oxygen deficient waters it can get incorporated into the solid phase authigenic by sulfide formation as Fe sulfides (Algeo and Maynard, 2004; Tribovillard et al., 2006). Co is prone to be influenced by detrital clastic material. The average Co concentration throughout the sediment core is ~11 ppm similar to the average crustal Co value of 10 ppm (Taylor and McLennan, 1995). Near similar values of Co with crustal values suggests its detrital contribution, but marginal enrichment in Co/Ti during LGM could be indicative of being a reasonable proxy to decipher past redox conditions.

Redox Proxy with Low Detrital Affect

Under oxic conditions, vanadium occurs in the form of V(V) as vanadate species getting adsorbed onto Mn-Fe oxyhydroxide (Morford and Emerson, 1999), whereas, Mo remains as unreactive dissolved molybdate species (${\text{MoO}}_4^{2-}$) (Emerson and Huested, 1991; Calvert and Pedersen, 1993; Tribovillard et al., 2006; Pattan and Pearce, 2009). Under oxygen deficient conditions, both V and Mo are removed from the water column and its enrichment in the sediment serves as potential tool to decipher reducing conditions at sediment-water interface (Calvert and Pedersen, 1993; Tribovillard et al., 2006; Pattan and Pearce, 2009).

The average V and Mo concentrations in the present study, are ~72 and ~1.4 ppm respectively. The co-occurrence of high values for Mo, V, OC, Mo/Ti, and V/Ti observed during LGM suggests prevalence of anoxic conditions at the sediment-water interface. Synchronous decline in Mo, V, OC, Mo/Ti, and V/Ti during deglacial period indicates resumption of oxic conditions at the sediment-water interface (Figures 3, 5). Unlike V and V/Ti, a conspicuous enrichment in OC, Mo, and Mo/Ti has been observed during early Holocene between 11 and 8 ka years BP. This can be corroborated well with the high sedimentation rate of ~13.5 cm.ka⁻¹ during early Holocene. This underpins better preservation of organic matter as a function of high sedimentation rate, while enhanced Mo and Mo/Ti plausibly resulted due to the formation of Mo-S complexes (Tribovillard et al., 2004).

In oxygenated waters, Mn is present as Mn (II) which is highly unstable and gets oxidized to insoluble Mn (IV) (Mn-oxyhydroxides) and is delivered to the sediments (Tribovillard et al., 2006). Manganese thus plays a significant role in transferring trace metals by scavenging them from the water column to the ocean bottom. However, during anoxic conditions, at the sediment-water interface, the dissolution of oxides and hydroxides releases Mn (II) back to the waters (Rajendran et al., 1992). Identical vertical distribution in V/Ti and Mn/Ti suggests adsorption of vanadate onto Fe- and Mn-oxyhydroxides (Calvert and Piper, 1984). The co-occurrence of high values of Mo/Ti and V/Ti during LGM suggests anoxic conditions, which results in dissolution of oxides and hydroxides and releasing Mn (II) back to the waters (Rajendran et al., 1992) leading to depletion of Mn concentration in the sediment. Contrarily, the simultaneous enrichment of V/Ti and Mo/Ti with Mn/Ti is observed along with the enhancement of CaCO₃ during LGM (Figure 4). Such conspicuous behavior of Mn can be attributed to trapping of Mn in authigenic Mn-carbonates during its export to the sediments (Pedersen and Price, 1982; Morford et al., 2001; Tribovillard et al., 2006).

Similar to V/Ti and Mo/Ti, enhanced values of Ni/Ti during LGM indicate its role as a redox sensitive proxy. Generally, Ni acts as a micronutrient and occurs as soluble cation either as Ni²⁺ in soluble nickel carbonate (NiCO₃) or NiCl⁺ in oxic environments (Calvert and Pedersen, 1993; Whitfield, 2001). The average Ni concentration (60 ppm) in the present study is higher than the average crustal abundance of 20 ppm (Taylor and McLennan, 1995). Simultaneous enhancement in Ni/Ti and OC during LGM suggest scavenging of Ni by organic matter in the water column (Piper and Perkins, 2004; Naimo et al., 2005). During organic matter degradation under extreme reducing conditions (sulfate redution), Ni generally precipitates as NiS in sediments. Therefore, high Ni/Ti along with OC during LGM implies deposition of the sediments under anoxic conditions. During deglacial period (17.5–10 ka years BP), synchronous decrease in Ni/Ti ratio and OC suggests oxic conditions in the sediment-water interface (Figure 5).

High OC and CaCO₃ values observed in the sediment core during LGM indicate enhanced productivity, whereas abrupt enhancement of OC during early Holocene (11–8 ka years BP) can be attributed to better preservation with high sedimentation rate. Similarly, enhanced redox sensitive elements (Mo/Ti, V/Ti, Ni/Ti) along with high OC during LGM suggests anoxic conditions triggered by high bacterial degradation of organic matter at the sediment-water interface. Unlike CaCO₃ and redox sensitive elements, marginal enrichment in the OC is observed at ~21 ka years BP which later declined, but CaCO₃ and redox sensitive elements showed consistently high values with declining pattern until 11 ka years BP. Moreover, the OC values are nearly similar at LGM and the early Holocene. Thus, during LGM, anoxic conditions persisted as indicated by redox sensitive elements, while no decipherable reducing conditions occurred during the early Holocene (11–8 ka years BP). A similar observation in SE Arabian Sea suggests high productivity induced low oxygenated bottom water conditions during LGM (Rao et al., 2010). In comparison to the present study, it has been reported that the sediments from the equatorial Arabian Sea (Pailler et al., 2002) and SE Arabian Sea (Pattan and Pearce, 2009) never witnessed complete anoxic bottom water conditions, instead a fluctuation between oxic and suboxic conditions has been observed during LGM. While, another study from the SE Arabian Sea suggests near-anoxic conditions probably resulting in enhanced OC preservation and removal of U from seawater during LGM (Sarkar et al., 1993).

Therefore, it can be stated that anomalous high OC values and changing behavior of redox sensitive elements suggests that it is not only the high sedimentation rate or organic matter degradation which influenced the redox elements, but other processes too are responsible for instigating the oxygen deficient conditions at the sediment-water interface during LGM.

Evidence of Anoxic Bottom Waters at LGM

The redox conditions at the sediment-water interface is mainly controlled by bottom water oxic conditions influenced by deep water circulation and increased oxygen demand for enhanced OC supply and its degradation (Pattan and Pearce, 2009; Pattan et al., 2013). Enhanced overhead productivity leads to greater organic matter export to the sediments. C/N ratios has been extensively used to decipher the provenance of organic matter, i.e., values of C/N ≤12 and C/N ≥12 suggests provenance of marine and terrestrial origin of OC respectively (Hedges and Parker, 1976; Emerson and Hedges, 1988; Meyers, 1997; Bhushan et al., 2001; Pattan et al., 2013). The C/N ratio in the present study varies from 9 to 17 with an average of 12. The C/N ratio followed pattern similar to Ti with low values during LGM with gradual increasing trend during the early Holocene followed by marginal decrease till present (Figure 6). Low C/N (~10) and high OC (~5 wt%) during LGM suggests reduced contribution of terrestrial OC primarily derived from overhead productivity. Marine OC is more labile and prone to microbial activity leading to oxygen deficient conditions both in water column and sediment-water interface. In the present study, if the enhanced peak of OC is due to high overhead productivity, then similar pattern should have been displayed by the redox sensitive elements during ~21 ka years BP. However, in the present scenario, the OC peak at ~21 ka years BP clearly indicates better preservation of OC (Figure 6).

FIGURE 6

Figure 6. Comparative plot for detrital and redox proxies with OC suggesting preservation of OC during LGM and early Holocene Period.

Due to the geographical setup, the deep water in the Indian Ocean is ventilated solely from south (Piotrowski et al., 2009). Previous studies on δ¹³C and δ¹⁸O isotopic composition of foraminifera suggested significant changes during the glacial-interglacial period in the chemical characteristics of surface and deep water masses (Duplessy, 1982; Naqvi et al., 1994; Schmiedl and Leuschner, 2005; Ahmad et al., 2008). NADW is the main source for deep water ventilation in the Northern Indian Ocean and marginal change in deep water circulation alters the bottom water oxygen conditions. Previous studies have suggested that during LGM, the export of deep water from north Atlantic was reduced, which further compensated increased formation of Southern Ocean deep water (Kallel et al., 1988; Ahmad et al., 2008) and allowed replacement of NADW with AABW penetrating further northward (Curry et al., 1988; Curry and Oppo, 2005).

The present study based on a sediment core raised from a water depth of 3,400 m demonstrates anoxic conditions during LGM in the equatorial Indian Ocean. Such anoxic conditions were established due to enhanced productivity with OC degradation and deep water circulation changes originating from weakly ventilated (poor in O₂ and rich CO₂) Southern Ocean deep waters. This further augmented oxygen deficient conditions causing enhanced preservation of OC. High OC peak at ~21 ka years BP can be attributed to post depositional preservation of organic matter at the sediment-water interface due to the bottom water anoxic conditions (Figure 6). The present observations of anoxic bottom water due to poor ventilation is further supported by Ahmad et al. (2008) and Piotrowski et al. (2009) from the equatorial Indian Ocean. They suggested weak deep-water ventilation in Northern Indian Ocean as a result of reduced proportion of NADW (poor in CO₂ and rich in O₂) and increased proportion of AABW (rich in CO₂ and poor in O₂) during LGM. During early Holocene (11–8 ka years BP), enhanced OC with C/N >12 (~16) suggests terrestrial origin of organic carbon (Figure 6). The OC preservation during the Holocene period without any significant variation in redox sensitive elements is mainly due to high sedimentation rate with deposition under well ventilated bottom water conditions.

Conclusions

The behavior of redox sensitive elements has been extensively used to decipher paleo redox conditions at the sediment-water interface. On the basis of investigation of redox sensitive elements and OC content in a sediment core from the equatorial Indian Ocean, the present study demonstrates prevalence of anoxic conditions during LGM. The anoxic condition in the water column at the sediment-water interface during ~21 ka years BP is due to the degradation of organic matter exported from enhanced overhead productivity further instigated by poorly ventilated bottom water. This results in post depositional preservation of OC. The early Holocene period (11–8 ka years BP) with increased OC has been attributed to high sedimentation rate supported by high overhead OC flux without any significant variation in the redox sensitive elements. The present study provides a valuable signature of poor bottom water ventilation at the equatorial Indian Ocean during LGM and its role in better OC preservation with concurrent occurrence of high surface productivity.

Author Contributions

All the authors have significantly contributed to bring the manuscript in final form. RB collected the samples. KC conducted the experiments and measurements. RB and KC compiled the data, interpreted, and prepared the manuscript. AJ provided radiocarbon AMS dates and chronology estimation of the sediment core.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We are thankful for the support of Ministry of Earth Sciences, Govt. of India under GEOTRACES Project (MOES/36/OOIS. Siber07). We thank cruise participants for their help and support during sediment core collection. We also thank Captain and Crew members of Sagar Kanya and NCAOR for providing logistic support during the cruise. We thank Director, PRL for support.

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