239 research outputs found

    Deepwater expansion and enhanced remineralization in the eastern equatorial Pacific during the last glacial maximum

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    Author Posting. © American Geophysical Union, 2018. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Paleoceanography and Paleoclimatology 33 (2018): 563-578, doi:10.1029/2017PA003221.Published estimates of the radiocarbon content of middepth waters suggest a decrease in ventilation in multiple locations during the last glacial maximum (LGM; 24.0–18.1 ka). Reduced glacial ventilation would have allowed respired carbon to accumulate in those waters. A subsequent deglacial release of this respired carbon reservoir to the atmosphere could then account for the observed increases in atmospheric CO2 and decline in atmospheric radiocarbon content. However, age model error and a release of 14C‐depleted mantle carbon have also been cited as possible explanations for the observed middepth radiocarbon depletions, calling into question the deep ocean's role in storing respired carbon during the LGM. Joint measurements of benthic foraminiferal carbon isotope values (δ13C) and cadmium/calcium (Cd/Ca) ratios provide a method for isolating the air‐sea component of a water mass from changes in remineralization. Here we use benthic foraminiferal δ13C and Cd/Ca records from the eastern equatorial Pacific to constrain changes in remineralization and water‐mass mixing over the last glacial‐interglacial transition. These records are complemented with elemental measurements of the authigenic coatings of foraminifera to monitor postdepositional changes in bottom water properties. Our results suggest an increase of deep waters at midwater depths consistent with a shoaling of the boundary between the upper and lower branches of Southern Ocean overturning circulation. Additionally, our records demonstrate increased organic matter remineralization in middepth waters during the LGM, suggesting that respired carbon did accumulate in middepth waters under periods of reduced ventilation.National Science foundation Grant Number: OCE‐09563682018-11-1

    Sea surface temperature changes in the southern California borderlands during the last glacial-interglacial cycle

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    A variety of evidence suggests that average sea surface temperatures (SSTs) during the last glacial maximum in the California Borderlands region were significantly colder than during the Holocene. Planktonic foraminiferal δ18O evidence and average SST estimates derived by the modern analog technique indicate that temperatures were 6°-10°C cooler during the last glacial relative to the present. The glacial plankton assemblage is dominated by the planktonic foraminifer Neogloboquadrina pachyderma (sinistral coiling) and the coccolith Coccolithus pelagicus, both of which are currently restricted to subpolar regions of the North Pacific. The glacial-interglacial average SST change determined in this study is considerably larger than the 2°C change estimated by Climate: Long-Range Investigation, Mapping, and Prediction (CLIMAP) [1981]. We propose that a strengthened California Current flow was associated with the advance of subpolar surface waters into the Borderlands region during the last glacial

    Western Arctic Ocean temperature variability during the last 8000 years

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    Author Posting. © American Geophysical Union, 2011. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 38 (2011): L24602, doi:10.1029/2011GL049714.We reconstructed subsurface (∼200–400 m) ocean temperature and sea-ice cover in the Canada Basin, western Arctic Ocean from foraminiferal δ18O, ostracode Mg/Ca ratios, and dinocyst assemblages from two sediment core records covering the last 8000 years. Results show mean temperature varied from −1 to 0.5°C and −0.5 to 1.5°C at 203 and 369 m water depths, respectively. Centennial-scale warm periods in subsurface temperature records correspond to reductions in summer sea-ice cover inferred from dinocyst assemblages around 6.5 ka, 3.5 ka, 1.8 ka and during the 15th century Common Era. These changes may reflect centennial changes in the temperature and/or strength of inflowing Atlantic Layer water originating in the eastern Arctic Ocean. By comparison, the 0.5 to 0.7°C warm temperature anomaly identified in oceanographic records from the Atlantic Layer of the Canada Basin exceeded reconstructed Atlantic Layer temperatures for the last 1200 years by about 0.5°C.J.R.F., T.M.C., and R.C.T. thank support by USGS Global Change Program, G.S.D. thanks support from the USGS Global Change Program and the NSF Office of Polar Programs, A.d.V. thanks support by Fond québécois de la recherché sur la nature et les technologies (FQRNT) and the Ministere du Développement économique, innovation et exportation (MDEIE) of Quebec.2012-06-1

    A study of the TEX86 paleothermometer in the water column and sediments of the Santa Barbara Basin, California

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    Particulate organic matter collected during a 2-year period, as part of an ongoing sediment trap study, and a high-resolution sediment record from 1850 to 1987 A.D. from the Santa Barbara Basin were analyzed for TEX86, a temperature proxy based on marine crenarchaeotal membrane lipids. Highest fluxes of crenarchaeotal lipids in the water column were found in May-June 1996 and from October 1996 to January 1997 and, in general, showed a good correlation with mass fluxes. TEX86 reconstructed temperatures from the sediment trap series ranged from 8 to 11°C and were usually substantially lower than sea surface temperatures (SST), indicating that unlike in previous studies, the TEX86 corresponds to subsurface temperatures, likely between 100 and 150 m. TEX86 temperature variations observed in trap samples were not coupled to changes in SST or deep-water temperatures and only to some degree with crenarchaeotal lipid fluxes. This suggests that a complex combination of different depth origins and seasonal growth periods of Crenarchaeota contributed to the variations in TEX86 signal during the annual cycle. TEX86 temperatures in the two sediment cores studied (8-13°C) were also substantially lower than those of instrumental SST records (14-17.5°C) confirming that TEX86 records a subsurface temperature signal in the Santa Barbara Basin. This result highlights the importance of performing calibration studies using sediment traps and core tops before applying the TEX86 temperature proxy in a given study area

    The Impacts of Flood, Drought, and Turbidites on Organic Carbon Burial Over the Past 2,000 years in the Santa Barbara Basin, California

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    Climate conditions and instantaneous depositional events can influence the relative contribution of sediments from terrestrial and marine environments and ultimately the quantity and composition of carbon buried in the sediment record. Here, we analyze the elemental, isotopic, and organic geochemical composition of marine sediments to identify terrestrial and marine sources in sediment horizons associated with droughts, turbidites, and floods in the Santa Barbara Basin (SBB), California, during the last 2,000 years. Stable isotopes (δ13C and δ15N) indicate that more terrestrial organic carbon (OC) was deposited during floods relative to background sediment, while bulk C to nitrogen (C/N) ratios remained relatively constant (~10). Long- chain n- alkanes (C27, C29, C31, and C33), characteristic of terrestrial OC, dominated all types of sediment deposition but were 4 times more abundant in flood layers. Marine algae (C15, C17, and C19) and macrophytes (C21 and C23) were also 2 times higher in flood versus background sediments. Turbidites contained twice the terrestrial n- alkanes relative to background sediment. Conversely, drought intervals were only distinguishable from background sediment by their higher proportion of marine algal n- alkanes. Combined, our data indicate that 15% of the total OC buried in SBB over the past 2,000 years was deposited during 11 flood events where the sediment was mostly terrestrially derived, and another 12% of deep sediment OC burial was derived from shelf remobilization during six turbidite events. Relative to twentieth century river runoff, our data suggest that floods result in considerable terrestrial OC burial on the continental margins of California.Key PointsTerrestrial organic carbon is the dominant source of carbon to the SBB with deposition significantly increasing during flood eventsEpisodic flood and turbidite remobilization events were responsible for over 25% of the OC buried in the SBB over the past 2,000 yearsDrought sedimentation had significantly lower sedimentation rates and had an n- alkane composition consistent with increased marine inputsPeer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/156217/4/palo20901-sup-0002-2020PA003849-fs01.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/156217/3/palo20901_am.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/156217/2/palo20901.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/156217/1/palo20901-sup-0003-2020PA003849-fs02.pd

    Rapid Organic Matter Sulfurization in Sinking Particles from the Cariaco Basin Water Column

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    Organic matter (OM) burial in marine sediments is a potentially important control on global climate and the long-term redox state of the earth’s surface. Still, we have only a limited understanding of the processes that stabilize OM and facilitate its preservation in the geologic record. Abiotic reactions with (poly)sulfides can enhance the preservation potential of OM, but for this process to be significant it needs to compete with OM remineralization, the majority of which occurs before sinking particles reach the sea floor. Here we investigate whether OM sulfurization occurs within sinking particles in the Cariaco Basin, a modern sulfidic marine environment with high rates of OM burial. Proto-kerogen in sinking particles is frequently more sulfur-rich and ^(34)S-depleted than expectations for biomass, with a composition that is difficult to explain by mixing with resuspended or terrigenous material. Instead, it appears that sulfur is being incorporated into OM on a timescale of days in sinking particles. The flux of this abiogenic organic S from particles is equivalent to approximately two-thirds of the total amount of proto-kerogen S at 10 cm depth in underlying sediments (ODP Core 1002B); after 6000 years of more gradual sulfurization reactions, potential water column sources are still equivalent to nearly half of the total proto-kerogen S in Cariaco sediments. Water column sulfurization is most extensive during periods of upwelling and high primary productivity and appears to involve elemental S, possibly via polysulfides. This process has the potential to deliver large amounts of OM to the sediments by making it less available for remineralization, generating OM-rich deposits. It represents a potentially dynamic sink in the global carbon cycle that can respond to changes in environmental conditions, including the size and intensity of O_2-depleted environments. Water column OM sulfurization could also have played a more significant role in the carbon cycle during ocean anoxic events, for example during the Cretaceous

    Magnitude and Composition of Sinking Particulate Phosphorus Fluxes in Santa Barbara Basin, California

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    [1] The composition and bioavailability of particulate P influence marine biological community production on both modern and geologic time‐scales, and continental margins play a critical role in the supply, modification, and storage of particulate P. This study examined particulate P cycling in the Santa Barbara Basin (SBB) off the coast of southern California using a ∼520 m deep‐moored sediment trap deployed from 1993–2006 and a sediment core collected in 2005 directly beneath the sediment trap at 590 m. Total particulate P (TPP), particulate inorganic P (PIP), and particulate organic P (POP) were quantified using a 5‐step sequential extraction method (SEDEX) that chemically separates PIP into loosely bound, oxide‐bound, authigenic, and detrital P phases. POP fluxes, while similar in magnitude to other coastal regions (22 ± 10 μmol m−2 d−1) were a small component of the TPP pool (15%). Seasonal trends revealed significant increases in POP fluxes during upwelling due to increased biological production in surface waters by organisms that increased mineral ballast. High particulate organic carbon (POC) to POP ratios (337 ± 18) further indicated rapid and efficient remineralization of POP relative to POC as particles sank through the oxic water column; however, further reduction of POP ceased in the deeper anoxic waters. Loosely bound, oxide‐bound, and authigenic P, dominated the TPP pool, with PIP fluxes substantially higher than those measured in other coastal settings. Strong correlations between oxide‐associated, authigenic, and detrital P fluxes with lithogenic material indicated a terrestrial source associated with riverine discharge. Furthermore, more than 30% of the loosely bound and oxide‐bound P was remineralized prior to burial, with the magnitude of dissolution far exceeding that of POP. These results highlight the dynamic nature of the particulate P pool in coastal ecosystems and how changes in P source can alter the composition and lability of P that enters coastal waters

    Calcification of the Planktonic Foraminiferaglobigerinabulloidesand Carbonate Ion Concentration Resultsfrom the Santa Barbara Basin

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    Planktonic foraminiferal calcification intensity, reflected by shell wall thickness, has been hypothesized to covary with the carbonate chemistry of seawater. Here we use both sediment trap and box core samples from the Santa Barbara Basin to evaluate the relationship between the calcification intensity of the planktonic foraminifera species Globigerina bulloides, measured by area density (µg/µm2), and the carbonate ion concentration of seawater ([CO32−]). We also evaluate the influence of both temperature and nutrient concentration ([PO43−]) on foraminiferal calcification and growth. The presence of two G. bulloides morphospecies with systematically different calcification properties and offset stable isotopic compositions was identified within sampling populations using distinguishing morphometric characteristics. The calcification temperature and by extension calcification depth of the more abundant “normal” G. bulloides morphospecies was determined using δ18O temperature estimates. Calcification depths vary seasonally with upwelling and were used to select the appropriate [CO32−], temperature, and [PO43−] depth measurements for comparison with area density. Seasonal upwelling in the study region also results in collinearity between independent variables complicating a straightforward statistical analysis. To address this issue, we use additional statistical diagnostics and a down core record to disentangle the respective roles of each parameter on G. bulloides calcification. Our results indicate that [CO32−] is the primary variable controlling calcification intensity while temperature influences shell size. We report a modern calibration for the normal G. bulloides morphospecies that can be used in down core studies of well‐preserved sediments to estimate past [CO32−]

    Interannual and Subdecadal Variability in the Nutrient Geochemistry of the Cariaco Basin

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    The CARIACO Ocean Time Series program has made monthly measurements of oxygen, nutrients, and carbon system parameters (∑CO2, alkalinity, pH) in the Cariaco Basin since 1996. At the same time, sediment traps have collected settling particles at four to five depths ranging from 150 to 1,200 m. The depth of the transition from oxic to anoxic conditions has fluctuated dramatically over the time series due to changes in the occurrence of Caribbean water intrusions into the deep basin. Nutrient concentrations in the deep basin have increased steadily with time in a proportion reflective of the elemental ratios in the settling organic matter, although N:P ratios in the water column (approximately 16:1) differ from ratios in the accumulating nutrients (11:1) and the settling flux (ranging between 5:1 and 12.5:1). This difference is likely due to changes in the source material for remineralization, either because of sizeable ecosystem changes or changes in the relative importance of the terrestrial input of inorganic P or scavenging of P by mineral precipitation near the oxic/anoxic interface. Alternatively, there may have been changes in the degree of preferential remineralization of P
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